Variant report

Variant	rs2811757
Chromosome Location	chr9:139795504-139795505
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ETS1	chr9:139795442-139796173	A549	lung:	n/a	n/a
2	CEBPB	chr9:139795490-139795837	A549	lung:	n/a	n/a
3	JUND	chr9:139795416-139797384	A549	lung:	n/a	n/a
4	RELA	chr9:139795400-139797411	GM18505	blood:	n/a	chr9:139797052-139797061 chr9:139797020-139797029 chr9:139797052-139797061 chr9:139797020-139797029
5	POLR2A	chr9:139795503-139795605	GM12878	blood:	n/a	n/a
6	EP300	chr9:139795352-139798269	A549	lung:	n/a	chr9:139796145-139796155 chr9:139796329-139796342
7	FOS	chr9:139795242-139796256	MCF10A-Er-Src	breast:	n/a	n/a
8	FOS	chr9:139795447-139796230	MCF10A-Er-Src	breast:	n/a	n/a
9	SP1	chr9:139795455-139798285	A549	lung:	n/a	chr9:139797084-139797096 chr9:139796308-139796318 chr9:139797085-139797095 chr9:139797084-139797096
10	CUX1	chr9:139795459-139795538	GM12878	blood:	n/a	n/a
11	GATA3	chr9:139795368-139798179	A549	lung:	n/a	n/a
12	SIN3AK20	chr9:139795359-139796088	A549	lung:	n/a	n/a
13	FOS	chr9:139795431-139796237	MCF10A-Er-Src	breast:	n/a	n/a
14	POLR2A	chr9:139795081-139797437	PANC-1	pancreas:	n/a	n/a
15	MTA3	chr9:139795402-139797488	GM12878	blood:	n/a	n/a
16	RUNX3	chr9:139795317-139795743	GM12878	blood:	n/a	n/a
17	BCL3	chr9:139795421-139797476	A549	lung:	n/a	chr9:139797347-139797356
18	SP1	chr9:139795188-139798278	A549	lung:	n/a	chr9:139797084-139797096 chr9:139796308-139796318 chr9:139797085-139797095 chr9:139797084-139797096
19	MAX	chr9:139795202-139797489	A549	lung:	n/a	chr9:139796992-139797001 chr9:139796994-139797001 chr9:139797085-139797095
20	NR3C1	chr9:139795406-139797393	A549	lung:	n/a	n/a
21	MYC	chr9:139795352-139798188	A549	lung:	n/a	chr9:139796992-139797001 chr9:139796994-139797001 chr9:139797085-139797095
22	NR3C1	chr9:139795451-139796768	A549	lung:	n/a	n/a
23	EP300	chr9:139795315-139796481	A549	lung:	n/a	chr9:139796145-139796155 chr9:139796329-139796342
24	REST	chr9:139795333-139797526	A549	lung:	n/a	chr9:139797031-139797051
25	FOSL2	chr9:139795046-139797461	A549	lung:	n/a	n/a
26	FOSL2	chr9:139795422-139796338	A549	lung:	n/a	n/a
27	POLR2A	chr9:139795394-139795728	HepG2	liver:	n/a	n/a
28	RUNX3	chr9:139795392-139795669	GM12878	blood:	n/a	n/a
29	MAX	chr9:139795464-139797287	A549	lung:	n/a	chr9:139796992-139797001 chr9:139796994-139797001 chr9:139797085-139797095
30	POLR2A	chr9:139795478-139795609	MCF-7	breast:	n/a	n/a
31	POLR2A	chr9:139795396-139795978	A549	lung:	n/a	n/a
32	POLR2A	chr9:139795410-139797413	GM12878	blood:	n/a	n/a
33	MAX	chr9:139794769-139798216	A549	lung:	n/a	chr9:139796992-139797001 chr9:139796994-139797001 chr9:139797085-139797095
34	TCF12	chr9:139795211-139798659	A549	lung:	n/a	chr9:139796145-139796154

No.	Distal block	Cell Line	Cell type
1	chr9:139741435..139745914-chr9:139791926..139799555,14	MCF-7	breast:
2	chr9:139792836..139799400-chr9:139842261..139846047,7	MCF-7	breast:
3	chr9:139756813..139762418-chr9:139794047..139799241,10	MCF-7	breast:
4	chr9:139750688..139755458-chr9:139795433..139799837,5	MCF-7	breast:
5	chr9:139780016..139781830-chr9:139794857..139797433,2	K562	blood:
6	chr9:139783203..139785610-chr9:139794854..139797810,2	K562	blood:
7	chr9:139741649..139744546-chr9:139793332..139795839,3	MCF-7	breast:
8	chr9:139795452..139797956-chr9:139962617..139965206,2	MCF-7	breast:
9	chr9:139755534..139766605-chr9:139787339..139798569,18	MCF-7	breast:
10	chr9:139795418..139796997-chr9:139886315..139888091,2	MCF-7	breast:
11	chr9:139745935..139747440-chr9:139794813..139796712,2	MCF-7	breast:
12	chr9:139791042..139798100-chr9:139837150..139840881,10	MCF-7	breast:
13	chr9:139794979..139797624-chr9:139802353..139803934,2	K562	blood:
14	chr9:139693022..139696090-chr9:139793195..139796394,4	MCF-7	breast:
15	chr9:139794720..139797503-chr9:139940161..139941750,2	MCF-7	breast:
16	chr9:139790926..139800327-chr9:139835284..139840384,15	MCF-7	breast:

Variant related genes	Relation type
TRAF2	TF binding region
ENSG00000186193	Chromatin interaction
ENSG00000272679	Chromatin interaction
ENSG00000054148	Chromatin interaction
ENSG00000176919	Chromatin interaction
ENSG00000159069	Chromatin interaction
ENSG00000177943	Chromatin interaction
ENSG00000127191	Chromatin interaction
ENSG00000266507	Chromatin interaction
ENSG00000107281	Chromatin interaction
ENSG00000107223	Chromatin interaction
ENSG00000148362	Chromatin interaction
ENSG00000213213	Chromatin interaction
ENSG00000184925	Chromatin interaction
ENSG00000273066	Chromatin interaction

Extended variants
information (count: 153 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:103)

rs_ID	r²[population]
rs10116850	0.86[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs10119096	0.94[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10123375	0.90[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs10735659	0.94[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10747036	0.82[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs10747037	0.90[CHB][hapmap];1.00[CHD][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap];0.83[MEX][hapmap];0.82[TSI][hapmap];0.83[YRI][hapmap];0.82[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs10747038	0.86[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs10747039	0.83[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs10747040	0.86[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs10781517	0.90[CHB][hapmap];1.00[CHD][hapmap];0.85[GIH][hapmap];0.85[JPT][hapmap];0.91[MEX][hapmap];0.85[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs10781519	0.86[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs10781520	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs10781521	0.89[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs10781524	1.00[JPT][hapmap]
rs10870140	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10870141	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11145913	0.81[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs11145918	0.88[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs12555238	0.82[JPT][hapmap]
rs13301872	0.90[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17250448	0.92[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1800631	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1806500	0.85[AMR][1000 genomes]
rs2077581	0.90[CHB][hapmap];1.00[JPT][hapmap]
rs2236544	0.90[CHB][hapmap];1.00[CHD][hapmap];0.86[GIH][hapmap];0.85[JPT][hapmap];0.87[MEX][hapmap];0.81[TSI][hapmap];0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs2386139	0.90[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs2386140	0.90[CHB][hapmap];0.87[CHD][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.92[ASN][1000 genomes]
rs2784032	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2784033	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2784074	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2784075	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2784076	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2784080	0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2784081	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2784084	0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2784085	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2784086	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2784087	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2784088	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2784095	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2784096	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2811758	0.86[ASW][hapmap];0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];0.89[TSI][hapmap];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2811759	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2811760	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2811761	1.00[ASW][hapmap];0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.96[MEX][hapmap];0.91[MKK][hapmap];0.92[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2811762	1.00[ASW][hapmap];0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.96[MEX][hapmap];0.91[MKK][hapmap];0.92[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2811763	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2811764	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3739942	0.90[CHB][hapmap];1.00[CHD][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap];0.87[MEX][hapmap];0.85[TSI][hapmap];0.83[YRI][hapmap];0.82[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs3739943	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.81[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs3750511	0.90[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs3750512	0.80[CHB][hapmap];1.00[JPT][hapmap]
rs4448378	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4567138	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4636298	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap];0.92[MEX][hapmap];0.93[TSI][hapmap];0.90[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4880071	0.85[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs4880074	0.95[ASN][1000 genomes]
rs4880075	0.95[ASN][1000 genomes]
rs4880076	0.90[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs4880147	0.87[ASN][1000 genomes]
rs4880148	0.83[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs4880149	0.84[ASN][1000 genomes]
rs4880152	0.84[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs4880153	0.90[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs4880154	0.83[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs4880157	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4880158	0.86[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.88[MKK][hapmap];0.81[TSI][hapmap];0.92[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4880159	0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4880160	1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.81[TSI][hapmap];0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4880161	1.00[CHB][hapmap];0.96[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs4880162	1.00[ASW][hapmap];0.90[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.91[MEX][hapmap];1.00[MKK][hapmap];0.85[TSI][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs4880163	0.90[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.91[MKK][hapmap];0.85[TSI][hapmap];1.00[YRI][hapmap];0.92[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs4880164	0.90[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs4880165	0.95[ASN][1000 genomes]
rs4880166	0.82[CEU][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs4880168	0.86[ASW][hapmap];0.82[CEU][hapmap];0.87[CHD][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.82[TSI][hapmap];0.84[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs6560650	0.81[AMR][1000 genomes]
rs7023607	0.86[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs7027246	0.90[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs7028413	0.86[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs7028806	0.94[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7028946	1.00[JPT][hapmap]
rs7030079	0.92[AMR][1000 genomes];0.80[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7034762	0.92[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs7037205	0.81[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs7039147	0.86[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs7039663	0.89[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs7047374	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];0.91[MKK][hapmap];0.93[TSI][hapmap];1.00[YRI][hapmap];0.94[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7048209	0.93[ASN][1000 genomes]
rs7048334	0.85[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs7048473	0.90[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs7048838	0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs7048940	0.92[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs7388748	0.94[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7854924	0.89[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs7868124	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7868660	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7868671	0.93[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7869864	0.90[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes]
rs7872595	0.92[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs872463	1.00[CHD][hapmap];1.00[JPT][hapmap];0.83[MEX][hapmap]
rs908831	0.80[CHB][hapmap];1.00[JPT][hapmap]
rs945385	0.80[CHB][hapmap];1.00[CHD][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap];0.87[MEX][hapmap];0.81[TSI][hapmap];0.81[AMR][1000 genomes];0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:50 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv430118	chr9:139101947-139795504	Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	299 gene(s)	inside rSNPs	diseases
2	nsv540342	chr9:139218422-139973312	Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Strong transcription Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	317 gene(s)	inside rSNPs	diseases
3	esv2758204	chr9:139252829-139826485	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	270 gene(s)	inside rSNPs	diseases
4	esv2759720	chr9:139252829-139826485	Weak transcription Enhancers Genic enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	270 gene(s)	inside rSNPs	diseases
5	nsv469918	chr9:139254317-140068342	Enhancers Active TSS Weak transcription Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	341 gene(s)	inside rSNPs	diseases
6	nsv540346	chr9:139360142-140164011	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	471 gene(s)	inside rSNPs	diseases
7	nsv1039149	chr9:139376829-139991102	Active TSS Enhancers Strong transcription Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	303 gene(s)	inside rSNPs	diseases
8	esv1803979	chr9:139395473-139979276	Genic enhancers Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	267 gene(s)	inside rSNPs	diseases
9	esv1831778	chr9:139395473-139979276	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	267 gene(s)	inside rSNPs	diseases
10	esv1821575	chr9:139395473-140068342	Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Bivalent TSS/Enh Strong transcription Weak transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	293 gene(s)	inside rSNPs	diseases
11	esv2422220	chr9:139478587-140244550	Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	454 gene(s)	inside rSNPs	diseases
12	nsv894409	chr9:139483954-139860264	Transcr. at gene 5' and 3' Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	209 gene(s)	inside rSNPs	diseases
13	nsv894432	chr9:139522101-139869914	Flanking Bivalent TSS/Enh Strong transcription Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	205 gene(s)	inside rSNPs	diseases
14	nsv894440	chr9:139544437-139841512	Active TSS Weak transcription Genic enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	194 gene(s)	inside rSNPs	diseases
15	nsv894441	chr9:139544437-139860264	Flanking Active TSS Weak transcription Bivalent Enhancer Strong transcription Bivalent/Poised TSS Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	201 gene(s)	inside rSNPs	diseases
16	nsv894442	chr9:139544437-140462099	Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	469 gene(s)	inside rSNPs	diseases
17	nsv894451	chr9:139598108-139995065	Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	200 gene(s)	inside rSNPs	diseases
18	nsv894452	chr9:139598108-140523429	Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	450 gene(s)	inside rSNPs	diseases
19	nsv894454	chr9:139607966-139904037	Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	172 gene(s)	inside rSNPs	diseases
20	nsv894455	chr9:139607966-140411547	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	417 gene(s)	inside rSNPs	diseases
21	nsv818738	chr9:139634495-139904037	Strong transcription Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	126 gene(s)	inside rSNPs	diseases
22	nsv894460	chr9:139683224-139810595	Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS Genic enhancers Enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	83 gene(s)	inside rSNPs	diseases
23	nsv894461	chr9:139683224-139860264	Strong transcription Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	97 gene(s)	inside rSNPs	diseases
24	nsv894462	chr9:139683224-140274164	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	353 gene(s)	inside rSNPs	diseases
25	nsv894463	chr9:139683224-140411547	Flanking Active TSS Bivalent/Poised TSS Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	376 gene(s)	inside rSNPs	diseases
26	nsv894465	chr9:139690144-139795504	Flanking Active TSS Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	76 gene(s)	inside rSNPs	diseases
27	esv1846327	chr9:139690144-139841512	Active TSS Genic enhancers Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	86 gene(s)	inside rSNPs	diseases
28	nsv524322	chr9:139690144-140376668	Genic enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	371 gene(s)	inside rSNPs	diseases
29	nsv894467	chr9:139693992-139810595	Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription Genic enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	77 gene(s)	inside rSNPs	diseases
30	nsv894468	chr9:139693992-139860264	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	92 gene(s)	inside rSNPs	diseases
31	nsv894469	chr9:139693992-140118448	Bivalent Enhancer Genic enhancers Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	200 gene(s)	inside rSNPs	diseases
32	nsv894470	chr9:139693992-140339091	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	358 gene(s)	inside rSNPs	diseases
33	nsv894473	chr9:139694521-139810595	Bivalent/Poised TSS Active TSS Strong transcription Weak transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	77 gene(s)	inside rSNPs	diseases
34	nsv894474	chr9:139694521-140432318	Genic enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	374 gene(s)	inside rSNPs	diseases
35	nsv540352	chr9:139695108-140351178	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	358 gene(s)	inside rSNPs	diseases
36	nsv894480	chr9:139700605-139795504	ZNF genes & repeats Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	74 gene(s)	inside rSNPs	diseases
37	nsv894481	chr9:139709976-139810595	Flanking Active TSS Enhancers Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	62 gene(s)	inside rSNPs	diseases
38	nsv894482	chr9:139709976-139860264	Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	78 gene(s)	inside rSNPs	diseases
39	nsv894483	chr9:139709976-139963091	Transcr. at gene 5' and 3' Enhancers Active TSS Strong transcription Genic enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	119 gene(s)	inside rSNPs	diseases
40	nsv894484	chr9:139709976-140382705	Flanking Active TSS Genic enhancers Enhancers Weak transcription Bivalent/Poised TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	360 gene(s)	inside rSNPs	diseases
41	nsv894485	chr9:139709976-140408904	Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	363 gene(s)	inside rSNPs	diseases
42	nsv894486	chr9:139725120-140382705	Bivalent Enhancer Strong transcription Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	359 gene(s)	inside rSNPs	diseases
43	nsv894487	chr9:139725120-140449582	Enhancers Bivalent/Poised TSS Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS Weak transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	363 gene(s)	inside rSNPs	diseases
44	nsv1047479	chr9:139754184-139869440	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	60 gene(s)	inside rSNPs	diseases
45	nsv540353	chr9:139754184-139869440	Enhancers Transcr. at gene 5' and 3' Weak transcription Genic enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	60 gene(s)	inside rSNPs	diseases
46	esv1803771	chr9:139776400-140274255	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	321 gene(s)	inside rSNPs	diseases
47	nsv894493	chr9:139781438-139820856	Weak transcription Genic enhancers Strong transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
48	nsv894494	chr9:139783292-139820856	Flanking Active TSS Strong transcription Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
49	nsv894495	chr9:139786465-139819625	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
50	nsv894496	chr9:139789093-139820363	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs2811757	C9orf142	cis	cerebellum	SCAN
rs2811757	GBGT1	cis	parietal	SCAN
rs2811757	PHPT1	cis	lymphoblastoid	seeQTL
rs2811757	NDOR1	cis	parietal	SCAN

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:139782200-139795600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
2	chr9:139782200-139795600	Weak transcription	Colon Smooth Muscle	Colon
3	chr9:139782200-139795600	Weak transcription	NHDF-Ad	bronchial
4	chr9:139782200-139796200	Weak transcription	Psoas Muscle	Psoas
5	chr9:139782200-139835800	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr9:139782200-139837000	Weak transcription	Fetal Brain Male	brain
7	chr9:139782400-139795600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
8	chr9:139783000-139823600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
9	chr9:139784000-139796000	Strong transcription	Fetal Stomach	stomach
10	chr9:139785000-139795800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
11	chr9:139785400-139801400	Weak transcription	Ovary	ovary
12	chr9:139785600-139812600	Strong transcription	Dnd41	blood
13	chr9:139792000-139823400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr9:139792400-139796000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr9:139792400-139796000	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr9:139792400-139796000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
17	chr9:139792600-139796000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
18	chr9:139792600-139796200	Strong transcription	Fetal Muscle Leg	muscle
19	chr9:139792600-139797400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr9:139792600-139823000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr9:139792800-139795600	Strong transcription	Fetal Muscle Trunk	muscle
22	chr9:139792800-139795800	Strong transcription	NHLF	lung
23	chr9:139792800-139796000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr9:139792800-139796200	Strong transcription	Placenta	Placenta
25	chr9:139792800-139796400	Strong transcription	Brain Cingulate Gyrus	brain
26	chr9:139792800-139797000	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr9:139792800-139797200	Strong transcription	Primary monocytes fromperipheralblood	blood
28	chr9:139792800-139797600	Strong transcription	Fetal Brain Female	brain
29	chr9:139792800-139798200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
30	chr9:139792800-139806200	Strong transcription	Monocytes-CD14+_RO01746	blood
31	chr9:139792800-139812600	Strong transcription	Cortex derived primary cultured neurospheres	brain
32	chr9:139793000-139796000	Strong transcription	Primary T cells from cord blood	blood
33	chr9:139793000-139797200	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr9:139793000-139798600	Strong transcription	HUES64 Cell Line	embryonic stem cell
35	chr9:139793000-139804200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr9:139793000-139805200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
37	chr9:139793000-139805400	Strong transcription	HUES48 Cell Line	embryonic stem cell
38	chr9:139793000-139806400	Strong transcription	Thymus	Thymus
39	chr9:139793000-139812600	Strong transcription	HUES6 Cell Line	embryonic stem cell
40	chr9:139793200-139795600	Strong transcription	Primary T cells fromperipheralblood	blood
41	chr9:139793200-139795600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
42	chr9:139793200-139795600	Strong transcription	Primary T helper cells PMA-I stimulated	--
43	chr9:139793200-139795600	Genic enhancers	HMEC	breast
44	chr9:139793200-139795800	Weak transcription	Small Intestine	intestine
45	chr9:139793200-139796000	Strong transcription	Brain Inferior Temporal Lobe	brain
46	chr9:139793200-139796200	Strong transcription	Brain Hippocampus Middle	brain
47	chr9:139793200-139796400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
48	chr9:139793200-139797600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr9:139793200-139798200	Genic enhancers	Fetal Intestine Small	intestine
50	chr9:139793200-139799800	Strong transcription	Brain Germinal Matrix	brain

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