Variant report

Variant	rs9393691
Chromosome Location	chr6:26272829-26272830
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	POLR2A	chr6:26270354-26274437	Raji	blood:	n/a	n/a
2	RELA	chr6:26272777-26273652	GM19099	blood:	n/a	n/a
3	POLR2A	chr6:26266613-26275023	H1-hESC	embryonic stem cell:	n/a	n/a
4	CHD1	chr6:26270342-26274429	GM12878	blood:	n/a	n/a
5	GATA1	chr6:26272469-26273436	PBDE	blood:	n/a	n/a
6	SP1	chr6:26272779-26273334	H1-hESC	embryonic stem cell:	n/a	chr6:26273080-26273101 chr6:26272906-26272927
7	CHD1	chr6:26269438-26274500	H1-hESC	embryonic stem cell:	n/a	n/a
8	RCOR1	chr6:26270357-26273588	Hela-S3	cervix:	n/a	n/a
9	POLR2A	chr6:26268846-26274052	Hela-S3	cervix:	n/a	n/a
10	POLR2A	chr6:26269656-26274808	H1-hESC	embryonic stem cell:	n/a	n/a
11	SP1	chr6:26272722-26273611	A549	lung:	n/a	chr6:26273080-26273101 chr6:26272906-26272927
12	ZKSCAN1	chr6:26272374-26273449	Hela-S3	cervix:	n/a	n/a
13	POLR2A	chr6:26272087-26274531	HUVEC	blood vessel:	n/a	n/a
14	POU2F2	chr6:26272789-26273718	GM12878	blood:	n/a	chr6:26273112-26273122 chr6:26273113-26273124 chr6:26273109-26273127 chr6:26273114-26273122 chr6:26273111-26273123 chr6:26273113-26273122 chr6:26273112-26273122 chr6:26273111-26273125 chr6:26273114-26273121 chr6:26273113-26273123 chr6:26273110-26273125
15	ATF2	chr6:26272151-26273859	H1-hESC	embryonic stem cell:	n/a	n/a
16	WRNIP1	chr6:26272656-26273627	GM12878	blood:	n/a	n/a
17	RUNX3	chr6:26272188-26273854	GM12878	blood:	n/a	n/a
18	RCOR1	chr6:26272712-26273605	GM12878	blood:	n/a	n/a
19	ATF2	chr6:26272563-26273821	GM12878	blood:	n/a	n/a
20	ZBTB33	chr6:26272745-26273844	SK-N-SH	brain:	n/a	n/a
21	ZNF143	chr6:26272641-26273386	GM12878	blood:	n/a	n/a
22	CEBPB	chr6:26272817-26273278	A549	lung:	n/a	chr6:26272998-26273009 chr6:26272908-26272916 chr6:26272999-26273010 chr6:26272998-26273011 chr6:26272998-26273011
23	NFIC	chr6:26272628-26273885	GM12878	blood:	n/a	n/a
24	CTCF	chr6:26272640-26272870	GM12864	blood:	n/a	n/a
25	NR2F2	chr6:26272656-26273287	MCF-7	breast:	n/a	chr6:26272987-26273002
26	RELA	chr6:26272748-26274560	GM10847	blood:	n/a	n/a
27	TBP	chr6:26272792-26273358	Hela-S3	cervix:	n/a	n/a
28	POLR2A	chr6:26272453-26274170	GM15510	blood:	n/a	n/a
29	TCF12	chr6:26272814-26274269	A549	lung:	n/a	chr6:26273093-26273100
30	POLR2A	chr6:26269040-26274454	Hela-S3	cervix:	n/a	n/a
31	PML	chr6:26272667-26274707	GM12878	blood:	n/a	n/a
32	CTCF	chr6:26272680-26272830	GM06990	blood:	n/a	n/a
33	MAFK	chr6:26272738-26273566	Hela-S3	cervix:	n/a	n/a
34	POLR2A	chr6:26272821-26274028	U87	brain:	n/a	n/a
35	MTA3	chr6:26269886-26274743	GM12878	blood:	n/a	n/a
36	SIN3AK20	chr6:26270143-26273935	MCF-7	breast:	n/a	n/a
37	MYBL2	chr6:26272669-26273512	HepG2	liver:	n/a	n/a
38	CHD2	chr6:26272591-26273394	Hela-S3	cervix:	n/a	n/a
39	MXI1	chr6:26272473-26273830	IMR90	lung:	n/a	n/a
40	RUNX3	chr6:26272430-26272846	GM12878	blood:	n/a	n/a
41	NR2F2	chr6:26272434-26273286	MCF-7	breast:	n/a	chr6:26272987-26273002
42	POLR2A	chr6:26272431-26274472	GM18951	blood:	n/a	n/a
43	SIN3AK20	chr6:26272696-26273869	MCF-7	breast:	n/a	n/a
44	EP300	chr6:26272770-26273847	SK-N-SH	brain:	n/a	n/a
45	FOXM1	chr6:26272807-26274345	GM12878	blood:	n/a	n/a
46	TAF7	chr6:26268962-26274860	H1-hESC	embryonic stem cell:	n/a	n/a
47	NFYB	chr6:26272783-26273330	GM12878	blood:	n/a	chr6:26273076-26273091 chr6:26273079-26273094 chr6:26272904-26272916 chr6:26273079-26273094 chr6:26273079-26273093 chr6:26272905-26272919 chr6:26273081-26273091
48	CEBPB	chr6:26272807-26273378	Hela-S3	cervix:	n/a	chr6:26272998-26273009 chr6:26272908-26272916 chr6:26272999-26273010 chr6:26272998-26273011 chr6:26272998-26273011
49	GTF2F1	chr6:26272691-26273349	H1-hESC	embryonic stem cell:	n/a	n/a
50	FOXM1	chr6:26272406-26273849	GM12878	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:207494905..207496421-chr6:26271169..26273910,2	MCF-7	breast:
2	chr5:177631246..177631924-chr6:26272486..26273166,2	Hela-S3	cervix:
3	chr6:26270251..26272974-chr6:27776913..27779571,3	MCF-7	breast:
4	chr6:26271163..26276024-chr6:27111926..27116309,5	MCF-7	breast:
5	chr6:26270357..26275628-chr6:27773210..27778290,5	MCF-7	breast:
6	chr6:26270978..26274693-chr6:27098356..27103484,7	MCF-7	breast:
7	chr6:26270164..26274435-chr6:27112425..27114820,4	MCF-7	breast:
8	chr6:26270273..26274919-chr6:27857077..27861037,6	MCF-7	breast:
9	chr6:26271344..26273410-chr6:26517921..26519773,2	MCF-7	breast:
10	chr12:69978181..69979981-chr6:26271470..26273073,2	MCF-7	breast:
11	chr6:26271682..26274545-chr6:27832998..27834644,2	MCF-7	breast:
12	chr19:1268856..1271453-chr6:26271863..26274067,2	MCF-7	breast:
13	chr6:26269718..26276565-chr6:27099393..27105112,10	MCF-7	breast:
14	chr14:50153414..50155005-chr6:26272692..26275211,2	MCF-7	breast:
15	chr13:36919647..36921156-chr6:26271932..26274514,2	MCF-7	breast:
16	chr12:100591588..100593211-chr6:26271479..26273991,2	MCF-7	breast:
17	chr1:156252625..156254328-chr6:26272141..26274407,2	MCF-7	breast:
18	chr6:26020614..26023729-chr6:26272152..26276212,4	MCF-7	breast:

Variant related genes	Relation type
HIST1H2APS4	TF binding region
HIST1H3G	TF binding region
HIST1H2BI	TF binding region
ENSG00000124635	Chromatin interaction
ENSG00000198366	Chromatin interaction
ENSG00000163472	Chromatin interaction
ENSG00000196787	Chromatin interaction
ENSG00000196176	Chromatin interaction
ENSG00000133104	Chromatin interaction
ENSG00000267493	Chromatin interaction
ENSG00000233224	Chromatin interaction
ENSG00000264405	Chromatin interaction
ENSG00000217862	Chromatin interaction
ENSG00000265565	Chromatin interaction
ENSG00000198374	Chromatin interaction
ENSG00000196747	Chromatin interaction
ENSG00000100479	Chromatin interaction
ENSG00000199289	Chromatin interaction
ENSG00000120664	Chromatin interaction
ENSG00000099622	Chromatin interaction
ENSG00000185130	Chromatin interaction
ENSG00000203813	Chromatin interaction
ENSG00000196352	Chromatin interaction
ENSG00000197153	Chromatin interaction
ENSG00000197903	Chromatin interaction
ENSG00000184825	Chromatin interaction
ENSG00000197451	Chromatin interaction
ENSG00000166226	Chromatin interaction
ENSG00000075089	Chromatin interaction

Extended variants
information (count: 68 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs1053860	0.92[JPT][hapmap]
rs10946808	0.82[JPT][hapmap]
rs10946810	0.81[CEU][hapmap];0.92[JPT][hapmap]
rs11755943	0.82[JPT][hapmap]
rs11759682	0.82[JPT][hapmap]
rs11759720	0.82[JPT][hapmap]
rs12525187	0.83[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12660432	0.80[EUR][1000 genomes]
rs12661552	0.81[EUR][1000 genomes]
rs12665035	0.81[CEU][hapmap];0.91[JPT][hapmap]
rs17608582	0.80[EUR][1000 genomes]
rs1883213	0.92[CEU][hapmap];0.89[GIH][hapmap];0.92[JPT][hapmap];0.81[EUR][1000 genomes]
rs1987244	0.82[EUR][1000 genomes]
rs1997768	0.82[JPT][hapmap]
rs2893820	0.92[CEU][hapmap];0.89[GIH][hapmap];0.92[JPT][hapmap];0.82[EUR][1000 genomes]
rs2893842	0.81[CEU][hapmap];0.82[JPT][hapmap]
rs2893843	1.00[CEU][hapmap];0.93[CHB][hapmap];0.91[JPT][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs3734533	0.82[JPT][hapmap]
rs3778279	0.92[JPT][hapmap]
rs3823157	0.82[JPT][hapmap]
rs4412192	0.81[GIH][hapmap]
rs4412193	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[CHD][hapmap];0.91[GIH][hapmap];0.91[JPT][hapmap];0.92[LWK][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs61324092	0.82[EUR][1000 genomes]
rs62394764	0.81[EUR][1000 genomes]
rs62394768	0.81[EUR][1000 genomes]
rs6901243	0.82[JPT][hapmap]
rs6908402	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6916289	0.81[GIH][hapmap]
rs6918325	0.80[EUR][1000 genomes]
rs6930616	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[CHD][hapmap];0.91[GIH][hapmap];0.91[JPT][hapmap];0.92[LWK][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6932584	0.89[JPT][hapmap]
rs725575	0.81[EUR][1000 genomes]
rs7755741	0.81[CEU][hapmap];0.82[JPT][hapmap]
rs7773004	0.86[ASN][1000 genomes]
rs811041	0.82[JPT][hapmap]
rs9357005	0.83[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9358913	0.82[JPT][hapmap]
rs9358914	0.80[CEU][hapmap];0.90[JPT][hapmap]
rs9358916	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9358918	0.91[ASW][hapmap];0.96[CEU][hapmap];0.85[CHB][hapmap];1.00[CHD][hapmap];0.91[GIH][hapmap];0.91[JPT][hapmap];0.92[LWK][hapmap];0.92[MEX][hapmap];0.97[TSI][hapmap];0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9358920	0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9358925	0.92[CEU][hapmap];0.92[JPT][hapmap];0.81[EUR][1000 genomes]
rs9358926	0.84[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap]
rs9358927	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[CHD][hapmap];0.91[GIH][hapmap];0.91[JPT][hapmap];0.92[LWK][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9366648	0.88[CEU][hapmap];0.89[GIH][hapmap];0.92[JPT][hapmap];0.81[EUR][1000 genomes]
rs9366650	0.83[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9379842	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9379844	0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9379846	0.80[EUR][1000 genomes]
rs9393693	1.00[YRI][hapmap]
rs9393696	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9393697	0.92[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs994379	0.80[GIH][hapmap];0.92[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1029920	chr6:25638507-26585842	Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1215 gene(s)	inside rSNPs	diseases
2	nsv538162	chr6:25638507-26585842	Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Weak transcription Strong transcription Enhancers 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 target site	1215 gene(s)	inside rSNPs	diseases
3	nsv1030351	chr6:25813178-26352046	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1189 gene(s)	inside rSNPs	diseases
4	nsv1023453	chr6:25853830-26528250	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1201 gene(s)	inside rSNPs	diseases
5	nsv1025237	chr6:25874326-26280867	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1166 gene(s)	inside rSNPs	diseases
6	nsv538163	chr6:25874326-26280867	Enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1166 gene(s)	inside rSNPs	diseases
7	nsv428137	chr6:25987413-26351920	Enhancers Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1181 gene(s)	inside rSNPs	diseases
8	nsv916992	chr6:25991630-26280921	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1159 gene(s)	inside rSNPs	diseases
9	nsv1028232	chr6:26005449-26319756	Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1171 gene(s)	inside rSNPs	diseases
10	nsv870314	chr6:26008435-26280807	Flanking Active TSS Enhancers Active TSS Genic enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1151 gene(s)	inside rSNPs	diseases
11	nsv1023457	chr6:26014014-26305407	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1170 gene(s)	inside rSNPs	diseases
12	nsv1023979	chr6:26026870-26287399	Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1113 gene(s)	inside rSNPs	diseases
13	nsv1015782	chr6:26026870-26323895	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1114 gene(s)	inside rSNPs	diseases
14	nsv1018665	chr6:26026870-26352046	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1116 gene(s)	inside rSNPs	diseases
15	nsv601173	chr6:26239404-26322524	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	184 gene(s)	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs9393691	WDR90	trans	parietal	SCAN
rs9393691	ACOT13	cis	cerebellum	SCAN
rs9393691	HIST1H3C	cis	parietal	SCAN
rs9393691	HIST1H4H	cis	cerebellum	SCAN

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:26269000-26274200	Active TSS	iPS-20b Cell Line	embryonic stem cell
2	chr6:26269000-26274800	Active TSS	iPS-15b Cell Line	embryonic stem cell
3	chr6:26269200-26273200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr6:26269200-26274600	Active TSS	ES-I3 Cell Line	embryonic stem cell
5	chr6:26269200-26274600	Active TSS	iPS-18 Cell Line	embryonic stem cell
6	chr6:26269400-26273400	Active TSS	Hela-S3	cervix
7	chr6:26269400-26274400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
8	chr6:26269400-26274400	Active TSS	HUES48 Cell Line	embryonic stem cell
9	chr6:26269400-26274800	Active TSS	H9 Cell Line	embryonic stem cell
10	chr6:26269400-26275000	Active TSS	H1 Cell Line	embryonic stem cell
11	chr6:26269800-26274400	Active TSS	HUES6 Cell Line	embryonic stem cell
12	chr6:26269800-26274400	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
13	chr6:26269800-26274800	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr6:26269800-26274800	Active TSS	NHLF	lung
15	chr6:26270000-26273000	Flanking Active TSS	NHEK	skin
16	chr6:26270000-26274200	Active TSS	HUES64 Cell Line	embryonic stem cell
17	chr6:26270000-26274600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr6:26270000-26274800	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr6:26270200-26274400	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr6:26270200-26274800	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr6:26270400-26273000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
22	chr6:26270400-26273600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr6:26270400-26274200	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr6:26270400-26275400	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr6:26270600-26274400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr6:26270600-26274600	Active TSS	Dnd41	blood
27	chr6:26270600-26274800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr6:26270600-26275000	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr6:26270800-26274600	Active TSS	GM12878-XiMat	blood
30	chr6:26271000-26273000	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
31	chr6:26271000-26274000	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
32	chr6:26271200-26273000	Flanking Active TSS	Primary B cells from peripheral blood	blood
33	chr6:26271200-26274400	Active TSS	Esophagus	oesophagus
34	chr6:26271200-26274400	Active TSS	Small Intestine	intestine
35	chr6:26271200-26274600	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
36	chr6:26271200-26274600	Bivalent/Poised TSS	Brain Substantia Nigra	brain
37	chr6:26271200-26274800	Active TSS	Right Ventricle	heart
38	chr6:26271200-26274800	Active TSS	HSMM	muscle
39	chr6:26271400-26274400	Bivalent/Poised TSS	Brain Angular Gyrus	brain
40	chr6:26271400-26274600	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
41	chr6:26271400-26274800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr6:26271400-26274800	Active TSS	Aorta	Aorta
43	chr6:26271400-26274800	Bivalent/Poised TSS	Colon Smooth Muscle	Colon
44	chr6:26271600-26273000	Enhancers	Lung	lung
45	chr6:26271600-26273200	Weak transcription	Gastric	stomach
46	chr6:26271600-26274600	Bivalent/Poised TSS	Brain Inferior Temporal Lobe	brain
47	chr6:26271600-26274800	Active TSS	Colonic Mucosa	Colon
48	chr6:26271600-26274800	Active TSS	Placenta Amnion	Placenta Amnion
49	chr6:26271600-26274800	Active TSS	Sigmoid Colon	Sigmoid Colon
50	chr6:26271800-26273000	Flanking Active TSS	Primary monocytes fromperipheralblood	blood

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