Variant report

Variant	rs7768108
Chromosome Location	chr6:26442786-26442787
allele	A/G
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	RFX5	chr6:26439051-26443264	SK-N-SH	brain:	n/a	chr6:26440672-26440680 chr6:26440696-26440705 chr6:26440662-26440677 chr6:26439759-26439772

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:26441674..26444658-chr6:26456493..26459926,5	K562	blood:
2	chr6:26440449..26443327-chr6:26444566..26448075,3	K562	blood:

Variant related genes	Relation type
BTN3A3	TF binding region
ENSG00000112763	Chromatin interaction
ENSG00000111801	Chromatin interaction

Extended variants
information (count: 173 )
Associated
traits (count: 6 )

rSNPs within LD-proxies of this variant (count:144)

rs_ID	r²[population]
rs10447390	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs10447391	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs10456047	1.00[CEU][hapmap];0.81[MEX][hapmap]
rs10456331	1.00[CEU][hapmap];0.81[MEX][hapmap]
rs10484441	1.00[CEU][hapmap];0.82[MEX][hapmap]
rs10807008	0.91[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.80[GIH][hapmap];1.00[LWK][hapmap];0.94[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10946820	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs10946821	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs10946823	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs10946824	1.00[ASW][hapmap];0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[ASN][1000 genomes]
rs10946825	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs10946826	1.00[ASW][hapmap];0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[ASN][1000 genomes]
rs10946827	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs10946828	1.00[ASN][1000 genomes]
rs10946829	1.00[ASW][hapmap];0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[ASN][1000 genomes]
rs10946830	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10946832	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1131936	0.93[CEU][hapmap];0.83[TSI][hapmap]
rs12191917	1.00[ASW][hapmap];0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[ASN][1000 genomes]
rs12193283	1.00[CEU][hapmap]
rs12194001	0.83[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs12194036	1.00[CEU][hapmap]
rs12194073	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs12194412	1.00[ASN][1000 genomes]
rs12196371	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12198993	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs12201546	0.92[ASW][hapmap];0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[ASN][1000 genomes]
rs12203108	1.00[ASN][1000 genomes]
rs12203120	1.00[ASN][1000 genomes]
rs12203176	1.00[CHD][hapmap];0.83[LWK][hapmap];0.84[YRI][hapmap]
rs12205476	1.00[CHB][hapmap];0.84[ASN][1000 genomes]
rs12206812	1.00[ASW][hapmap];0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[ASN][1000 genomes]
rs12206839	1.00[ASN][1000 genomes]
rs12207930	1.00[ASW][hapmap];0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[ASN][1000 genomes]
rs12208211	1.00[CEU][hapmap];0.82[MEX][hapmap]
rs12208272	0.85[CEU][hapmap];0.82[MEX][hapmap]
rs12208329	1.00[ASN][1000 genomes]
rs12208788	0.93[CEU][hapmap];0.83[TSI][hapmap]
rs12211872	1.00[CEU][hapmap]
rs12213625	1.00[ASN][1000 genomes]
rs12214444	0.92[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.95[LWK][hapmap];0.88[MEX][hapmap];0.95[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12214486	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs12214924	1.00[ASW][hapmap];0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[ASN][1000 genomes]
rs12214976	1.00[ASN][1000 genomes]
rs12661560	1.00[CEU][hapmap]
rs12662604	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12664899	0.93[CEU][hapmap];1.00[CHB][hapmap];0.91[YRI][hapmap];0.84[ASN][1000 genomes]
rs16891681	0.82[LWK][hapmap]
rs17537465	0.93[CEU][hapmap];1.00[CHB][hapmap];0.92[YRI][hapmap];0.84[ASN][1000 genomes]
rs17539219	1.00[ASW][hapmap];0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[ASN][1000 genomes]
rs17610161	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.80[GIH][hapmap];0.87[LWK][hapmap];0.94[MEX][hapmap];1.00[MKK][hapmap];0.91[TSI][hapmap];0.91[YRI][hapmap];0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17611220	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs17611438	1.00[ASW][hapmap];0.85[CEU][hapmap];1.00[CHB][hapmap]
rs1884945	1.00[CEU][hapmap];0.82[MEX][hapmap]
rs2393652	1.00[ASW][hapmap];0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.92[ASN][1000 genomes]
rs2393655	1.00[ASN][1000 genomes]
rs2393656	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2393664	0.81[CEU][hapmap]
rs28571747	1.00[ASN][1000 genomes]
rs2893844	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs2893845	1.00[ASW][hapmap];0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[ASN][1000 genomes]
rs2893846	1.00[ASN][1000 genomes]
rs2893847	1.00[ASW][hapmap];0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.86[YRI][hapmap];1.00[ASN][1000 genomes]
rs2893848	1.00[ASW][hapmap];0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.86[YRI][hapmap];1.00[ASN][1000 genomes]
rs2893849	0.93[CEU][hapmap]
rs2893856	0.93[CEU][hapmap]
rs2893857	1.00[CEU][hapmap];0.82[MEX][hapmap]
rs3198487	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs3208734	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs34268421	1.00[ASN][1000 genomes]
rs3807025	1.00[ASN][1000 genomes]
rs3846843	1.00[ASW][hapmap];0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[ASN][1000 genomes]
rs3846844	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs3846847	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs3846848	1.00[ASW][hapmap];0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.83[MEX][hapmap];1.00[ASN][1000 genomes]
rs3846849	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs3902051	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.80[GIH][hapmap];0.88[MEX][hapmap];0.95[TSI][hapmap];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3903661	1.00[ASN][1000 genomes]
rs4083469	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs4305717	1.00[ASN][1000 genomes]
rs45499696	1.00[ASN][1000 genomes]
rs4609015	1.00[ASW][hapmap];0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[ASN][1000 genomes]
rs4711108	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4711109	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs4711110	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4711111	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs4712986	0.93[CEU][hapmap];0.83[TSI][hapmap]
rs4712988	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.88[MEX][hapmap];0.95[TSI][hapmap]
rs4712989	0.83[AFR][1000 genomes];0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4712990	0.91[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];0.96[LWK][hapmap];0.88[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4712992	1.00[ASN][1000 genomes]
rs4712993	1.00[ASW][hapmap];0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[ASN][1000 genomes]
rs4712994	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[ASN][1000 genomes]
rs4712995	1.00[ASN][1000 genomes]
rs4712996	1.00[ASW][hapmap];0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[ASN][1000 genomes]
rs4712999	0.92[CEU][hapmap]
rs4713000	1.00[CEU][hapmap]
rs4713001	1.00[CEU][hapmap];0.82[MEX][hapmap]
rs55775018	1.00[ASN][1000 genomes]
rs55786210	1.00[ASN][1000 genomes]
rs55957716	1.00[ASN][1000 genomes]
rs55994013	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56023587	0.83[AFR][1000 genomes];0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56143200	1.00[ASN][1000 genomes]
rs56157336	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56161420	1.00[ASN][1000 genomes]
rs56182232	1.00[ASN][1000 genomes]
rs56190518	1.00[ASN][1000 genomes]
rs56207464	1.00[ASN][1000 genomes]
rs56280732	1.00[ASN][1000 genomes]
rs56325223	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57275245	1.00[ASN][1000 genomes]
rs60750900	1.00[ASN][1000 genomes]
rs6456716	1.00[CHD][hapmap];0.83[LWK][hapmap];0.90[MKK][hapmap]
rs6456721	1.00[ASN][1000 genomes]
rs6456722	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs6456724	0.93[CEU][hapmap]
rs6900725	1.00[ASW][hapmap];0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[ASN][1000 genomes]
rs6901245	0.84[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs6910023	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs6912934	0.93[CEU][hapmap]
rs6920986	1.00[ASW][hapmap];0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[ASN][1000 genomes]
rs6926878	1.00[ASW][hapmap];0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[ASN][1000 genomes]
rs6928454	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs6929846	0.86[CEU][hapmap]
rs6931648	1.00[ASN][1000 genomes]
rs72841540	0.84[ASN][1000 genomes]
rs7355	0.93[CEU][hapmap];0.83[TSI][hapmap]
rs7356849	0.93[CEU][hapmap];0.83[TSI][hapmap]
rs7744254	1.00[ASW][hapmap];0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[ASN][1000 genomes]
rs7745238	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs7745767	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs7751280	1.00[ASW][hapmap];0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[ASN][1000 genomes]
rs7754940	1.00[ASN][1000 genomes]
rs7755398	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7770214	1.00[ASW][hapmap];0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[ASN][1000 genomes]
rs7770699	1.00[ASN][1000 genomes]
rs7775365	1.00[ASN][1000 genomes]
rs882010	1.00[CEU][hapmap]
rs9104	1.00[CHD][hapmap]
rs9295690	0.81[CEU][hapmap]
rs9461245	1.00[CHD][hapmap];0.91[LWK][hapmap];0.90[MKK][hapmap];0.92[YRI][hapmap]
rs9467759	0.93[CEU][hapmap]
rs9688949	1.00[CHD][hapmap]

Variant overlapped rSNPs/rCNVs (count:29 , 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	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
4	nsv482729	chr6:26291011-26470898	Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer Genic enhancers 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 target site	45 gene(s)	inside rSNPs	diseases
5	nsv482836	chr6:26352883-26520964	Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
6	nsv883493	chr6:26367689-26442786	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
7	nsv883494	chr6:26367833-26442786	Enhancers Genic enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
8	nsv883495	chr6:26367833-26443853	Weak transcription Strong transcription Enhancers Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
9	esv3334611	chr6:26367893-26443308	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
10	nsv482407	chr6:26369320-26550148	Active TSS Strong transcription Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	62 gene(s)	inside rSNPs	diseases
11	nsv883497	chr6:26369549-26442786	Flanking Active TSS Active TSS Strong transcription Weak transcription Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
12	nsv883498	chr6:26369549-26443853	Strong transcription Flanking Active TSS Weak transcription Active TSS Enhancers Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
13	nsv883499	chr6:26377591-26454454	Enhancers Flanking Active TSS Genic enhancers Active TSS Weak transcription Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
14	esv3427999	chr6:26378373-26453532	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
15	nsv462664	chr6:26379537-26451553	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
16	nsv601184	chr6:26379537-26451553	Active TSS Genic enhancers Weak transcription Flanking Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
17	esv2763996	chr6:26423901-26465384	Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
18	nsv1017824	chr6:26425410-26465384	Strong transcription Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
19	nsv1030289	chr6:26428314-26464017	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
20	nsv1033003	chr6:26428314-26465384	Transcr. at gene 5' and 3' Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
21	nsv1031229	chr6:26428314-26467182	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
22	nsv1031238	chr6:26428314-26471596	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
23	nsv1024483	chr6:26429262-26465384	Flanking Active TSS Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Weak transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
24	nsv1034561	chr6:26429262-26467182	Enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
25	nsv528172	chr6:26430981-26463660	Genic enhancers Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription 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 target site	15 gene(s)	inside rSNPs	diseases
26	nsv1029357	chr6:26432815-26464789	Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
27	nsv1023581	chr6:26432815-26465384	Enhancers Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
28	nsv1024222	chr6:26432815-26467182	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
29	nsv1022309	chr6:26434914-26464789	Enhancers Strong transcription Active TSS Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases

mRNA abundance (count:6)

SNP	Gene	Cis/trans	Tissue	Source
rs7768108	BTN2A1	cis	parietal	SCAN
rs7768108	LRRC16A	cis	parietal	SCAN
rs7768108	BTN2A3P	cis	Esophagus Muscularis	GTEx
rs7768108	GMNN	cis	parietal	SCAN
rs7768108	BTN2A2	Cis_1M	lymphoblastoid	RTeQTL
rs7768108	BTN3A1	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:89 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:26439600-26443000	Active TSS	Rectal Mucosa Donor 29	rectum
2	chr6:26440200-26442800	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
3	chr6:26441000-26442800	Flanking Active TSS	Primary B cells from cord blood	blood
4	chr6:26441000-26443000	Flanking Active TSS	Dnd41	blood
5	chr6:26441000-26443200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
6	chr6:26441200-26443000	Flanking Active TSS	Primary T cells from cord blood	blood
7	chr6:26441200-26444200	Weak transcription	Spleen	Spleen
8	chr6:26441200-26444600	Weak transcription	Gastric	stomach
9	chr6:26441200-26444600	Weak transcription	Skeletal Muscle Male	skeletal muscle
10	chr6:26441200-26444600	Weak transcription	K562	blood
11	chr6:26441200-26446400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr6:26441200-26449600	Weak transcription	Esophagus	oesophagus
13	chr6:26441200-26457000	Weak transcription	Brain Substantia Nigra	brain
14	chr6:26441200-26457600	Weak transcription	Pancreas	Pancrea
15	chr6:26441400-26442800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
16	chr6:26441400-26444400	Weak transcription	Fetal Muscle Trunk	muscle
17	chr6:26441400-26444600	Weak transcription	Small Intestine	intestine
18	chr6:26441400-26444800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr6:26441400-26445600	Weak transcription	Aorta	Aorta
20	chr6:26441400-26448200	Weak transcription	Right Ventricle	heart
21	chr6:26441400-26453000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr6:26441400-26455600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr6:26441400-26457000	Weak transcription	Brain Anterior Caudate	brain
24	chr6:26441400-26457400	Weak transcription	Psoas Muscle	Psoas
25	chr6:26441600-26442800	Enhancers	Primary hematopoietic stem cells short term culture	blood
26	chr6:26441600-26442800	Enhancers	NHDF-Ad	bronchial
27	chr6:26441600-26443000	Enhancers	Stomach Mucosa	stomach
28	chr6:26441600-26445000	Weak transcription	Thymus	Thymus
29	chr6:26441600-26446000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr6:26441600-26448000	Weak transcription	Placenta	Placenta
31	chr6:26441600-26448800	Weak transcription	Fetal Intestine Large	intestine
32	chr6:26441600-26451200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
33	chr6:26441600-26452400	Weak transcription	HSMMtube	muscle
34	chr6:26441600-26452800	Weak transcription	HSMM	muscle
35	chr6:26442000-26442800	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
36	chr6:26442000-26443000	Enhancers	Breast Myoepithelial Primary Cells	Breast
37	chr6:26442000-26443000	Enhancers	Fetal Thymus	thymus
38	chr6:26442000-26443200	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
39	chr6:26442000-26443200	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
40	chr6:26442000-26443200	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
41	chr6:26442200-26443000	Enhancers	Primary B cells from peripheral blood	blood
42	chr6:26442200-26443000	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
43	chr6:26442200-26443000	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
44	chr6:26442200-26443000	Weak transcription	NH-A	brain
45	chr6:26442200-26443200	Flanking Active TSS	Primary T cells fromperipheralblood	blood
46	chr6:26442200-26443200	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
47	chr6:26442200-26444800	Weak transcription	Colon Smooth Muscle	Colon
48	chr6:26442200-26447000	Weak transcription	Fetal Intestine Small	intestine
49	chr6:26442200-26449200	Weak transcription	HUVEC	blood vessel
50	chr6:26442200-26455800	Weak transcription	HepG2	liver

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