Variant report

Variant	rs869736
Chromosome Location	chr11:67205462-67205463
allele	G/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	chr11:67198736-67211579	HL-60	blood:	n/a	n/a
2	POLR2A	chr11:67205080-67206527	HUVEC	blood vessel:	n/a	n/a
3	RELA	chr11:67203641-67205476	GM18951	blood:	n/a	n/a
4	WRNIP1	chr11:67204991-67205534	GM12878	blood:	n/a	n/a
5	POLR2A	chr11:67203727-67205685	K562	blood:	n/a	n/a
6	POLR2A	chr11:67200617-67205780	GM12878	blood:	n/a	n/a
7	POLR2A	chr11:67200521-67212166	K562	blood:	n/a	n/a
8	POLR2A	chr11:67199088-67207292	GM18505	blood:	n/a	n/a
9	POLR2A	chr11:67199177-67206380	GM19099	blood:	n/a	n/a
10	POLR2A	chr11:67198947-67207334	HL-60	blood:	n/a	n/a
11	POLR2A	chr11:67204900-67205464	ProgFib	skin:	n/a	n/a
12	MXI1	chr11:67203597-67205479	GM12878	blood:	n/a	chr11:67205214-67205223
13	MAX	chr11:67205287-67205510	K562	blood:	n/a	n/a
14	POLR2A	chr11:67205014-67205500	A549	lung:	n/a	n/a
15	POLR2A	chr11:67201705-67209206	PFSK-1	brain:	n/a	n/a
16	PML	chr11:67200370-67206421	GM12878	blood:	n/a	n/a
17	MYC	chr11:67203883-67206373	NB4	blood:	n/a	n/a
18	POU2F2	chr11:67204668-67205516	GM12891	blood:	n/a	chr11:67205222-67205234 chr11:67204739-67204751 chr11:67204776-67204788 chr11:67204669-67204681
19	MAX	chr11:67203826-67206433	NB4	blood:	n/a	n/a
20	STAT5A	chr11:67200137-67206130	GM12878	blood:	n/a	chr11:67204620-67204631 chr11:67204709-67204716 chr11:67203878-67203890 chr11:67200355-67200367 chr11:67201441-67201453 chr11:67202211-67202219 chr11:67204675-67204687 chr11:67205486-67205498 chr11:67201551-67201563 chr11:67204583-67204591 chr11:67203902-67203913
21	PAX5	chr11:67203711-67205585	GM12878	blood:	n/a	chr11:67204707-67204716
22	MTA3	chr11:67204978-67205595	GM12878	blood:	n/a	n/a
23	POLR2A	chr11:67204690-67206893	H1-hESC	embryonic stem cell:	n/a	n/a
24	POLR2A	chr11:67205021-67205676	K562	blood:	n/a	n/a
25	FOXM1	chr11:67203291-67205608	GM12878	blood:	n/a	n/a
26	POLR2A	chr11:67199010-67205520	GM12892	blood:	n/a	n/a
27	POLR2A	chr11:67204881-67211417	Hela-S3	cervix:	n/a	n/a
28	POLR2A	chr11:67204617-67208372	PANC-1	pancreas:	n/a	n/a
29	POLR2A	chr11:67198625-67205482	GM12891	blood:	n/a	n/a
30	RFX5	chr11:67205272-67205642	Hela-S3	cervix:	n/a	n/a
31	POLR2A	chr11:67204867-67206145	MCF10A-Er-Src	breast:	n/a	n/a
32	POLR2A	chr11:67199678-67205474	GM18526	blood:	n/a	n/a
33	POLR2A	chr11:67204930-67205970	HepG2	liver:	n/a	n/a
34	POLR2A	chr11:67204710-67206005	H1-hESC	embryonic stem cell:	n/a	n/a
35	POLR2A	chr11:67201074-67209001	PFSK-1	brain:	n/a	n/a
36	POLR2A	chr11:67202451-67208499	SK-N-MC	brain:	n/a	n/a
37	POLR2A	chr11:67199974-67206444	GM12892	blood:	n/a	n/a
38	POLR2A	chr11:67198635-67206407	GM12891	blood:	n/a	n/a
39	POLR2A	chr11:67204657-67209717	ECC-1	luminal epithelium:	n/a	n/a
40	POLR2A	chr11:67200968-67205480	GM12878	blood:	n/a	n/a
41	POLR2A	chr11:67200187-67206414	GM15510	blood:	n/a	n/a
42	MTA3	chr11:67198952-67207449	GM12878	blood:	n/a	n/a
43	POLR2A	chr11:67203858-67206347	NB4	blood:	n/a	n/a
44	POLR2A	chr11:67204338-67206563	GM12878	blood:	n/a	n/a
45	POLR2A	chr11:67198622-67210790	GM12892	blood:	n/a	n/a
46	ELF1	chr11:67204344-67206363	GM12878	blood:	n/a	chr11:67204660-67204672
47	POLR2A	chr11:67198810-67206466	GM12878	blood:	n/a	n/a
48	CHD1	chr11:67203893-67205564	GM12878	blood:	n/a	n/a
49	STAT5A	chr11:67204683-67205582	GM12878	blood:	n/a	chr11:67204709-67204716 chr11:67205486-67205498
50	POLR2A	chr11:67204834-67211350	MCF-7	breast:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:67119575..67122290-chr11:67202664..67205561,2	K562	blood:
2	chr11:67201617..67208575-chr11:67270788..67277143,13	K562	blood:
3	chr11:67204954..67212426-chr11:67228820..67232211,6	K562	blood:
4	chr11:67138865..67141337-chr11:67205315..67206965,2	K562	blood:
5	chr11:67205296..67207654-chr11:67248873..67250891,2	MCF-7	breast:
6	chr11:67133399..67135942-chr11:67204970..67207093,2	K562	blood:

Variant related genes	Relation type
ENSG00000255949	TF binding region
ENSG00000110711	Chromatin interaction
ENSG00000167797	Chromatin interaction
ENSG00000175505	Chromatin interaction
ENSG00000270169	Chromatin interaction
ENSG00000256514	Chromatin interaction
ENSG00000110697	Chromatin interaction
ENSG00000175482	Chromatin interaction

Extended variants
information (count: 64 )
Associated
traits (count: 20 )

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10274	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];1.00[TSI][hapmap];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11227793	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11601325	0.89[CEU][hapmap];0.94[GIH][hapmap];0.83[MEX][hapmap];0.93[TSI][hapmap];0.87[EUR][1000 genomes]
rs12288107	0.82[CHD][hapmap]
rs12290164	0.82[CHD][hapmap]
rs12573992	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12787021	0.89[ASW][hapmap];1.00[CEU][hapmap];0.80[CHD][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.97[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13859	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1476792	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[MEX][hapmap];0.87[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1626067	1.00[ASW][hapmap]
rs1628442	0.88[AFR][1000 genomes];0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1638555	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1638556	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.96[LWK][hapmap];0.96[MEX][hapmap];0.97[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1638557	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1638565	0.89[AFR][1000 genomes];0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1638588	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];0.98[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17501521	0.85[GIH][hapmap]
rs1790733	0.80[CHD][hapmap]
rs1790752	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1790753	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1790761	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1808279	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1893973	0.88[EUR][1000 genomes]
rs2109123	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2276118	0.83[CHB][hapmap];0.84[JPT][hapmap];0.91[TSI][hapmap]
rs2302264	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.94[JPT][hapmap];0.96[MEX][hapmap];1.00[TSI][hapmap];0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs35787427	0.86[EUR][1000 genomes]
rs36089024	0.87[EUR][1000 genomes]
rs3741168	1.00[ASW][hapmap];1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[CHD][hapmap];0.94[GIH][hapmap];0.94[JPT][hapmap];1.00[LWK][hapmap];0.96[MEX][hapmap];0.90[MKK][hapmap];0.98[TSI][hapmap];0.84[YRI][hapmap];0.95[AFR][1000 genomes];0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4084113	0.81[CEU][hapmap];0.85[GIH][hapmap];0.83[MEX][hapmap];0.89[TSI][hapmap]
rs4465371	0.81[GIH][hapmap];0.84[TSI][hapmap]
rs4930427	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs595130	0.81[AFR][1000 genomes];0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs61889868	0.85[AFR][1000 genomes];0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs630172	1.00[ASW][hapmap];1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[CHD][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.91[MEX][hapmap];0.98[TSI][hapmap];0.84[YRI][hapmap];0.91[AFR][1000 genomes];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7110021	0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7114510	0.89[CEU][hapmap];0.94[GIH][hapmap];0.83[MEX][hapmap];0.93[TSI][hapmap];0.87[EUR][1000 genomes]
rs7131041	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7479801	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];1.00[TSI][hapmap];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs872375	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs917570	0.81[CEU][hapmap];0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:23 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531397	chr11:66653381-67465721	Active TSS Enhancers Strong transcription Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	271 gene(s)	inside rSNPs	diseases
2	nsv897797	chr11:67023040-67293234	Flanking Active TSS Strong transcription Enhancers Active TSS Weak transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	206 gene(s)	inside rSNPs	diseases
3	nsv1043037	chr11:67027193-67357425	Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Weak transcription Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	213 gene(s)	inside rSNPs	diseases
4	nsv897801	chr11:67033076-67432479	Bivalent Enhancer Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	236 gene(s)	inside rSNPs	diseases
5	nsv1048230	chr11:67058231-67252397	Active TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	146 gene(s)	inside rSNPs	diseases
6	nsv897804	chr11:67090571-67224278	Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	103 gene(s)	inside rSNPs	diseases
7	nsv1039205	chr11:67135246-67252397	Enhancers Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	122 gene(s)	inside rSNPs	diseases
8	esv1818769	chr11:67138811-67300457	Flanking Active TSS Active TSS Genic enhancers Weak transcription Enhancers Strong transcription 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 miRNA target site	167 gene(s)	inside rSNPs	diseases
9	esv1798859	chr11:67139954-67272983	Active TSS Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer 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	154 gene(s)	inside rSNPs	diseases
10	nsv897805	chr11:67155210-67283891	ZNF genes & repeats Flanking Active TSS Genic enhancers Enhancers Weak transcription Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	148 gene(s)	inside rSNPs	diseases
11	nsv897806	chr11:67155210-67294308	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	148 gene(s)	inside rSNPs	diseases
12	nsv897807	chr11:67155210-67414492	Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	176 gene(s)	inside rSNPs	diseases
13	nsv897808	chr11:67155210-67419855	Flanking Active TSS Strong transcription Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	176 gene(s)	inside rSNPs	diseases
14	nsv897809	chr11:67156875-67276235	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Strong transcription Weak transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	148 gene(s)	inside rSNPs	diseases
15	nsv555254	chr11:67164495-67288594	Weak transcription Flanking Active TSS Active TSS Genic enhancers Enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	146 gene(s)	inside rSNPs	diseases
16	nsv534229	chr11:67164667-67411909	Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	175 gene(s)	inside rSNPs	diseases
17	nsv897811	chr11:67166984-67218909	Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
18	nsv897813	chr11:67175692-67283891	Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	132 gene(s)	inside rSNPs	diseases
19	nsv521723	chr11:67175692-67311258	Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	132 gene(s)	inside rSNPs	diseases
20	esv1847460	chr11:67182600-67219337	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
21	nsv524096	chr11:67186000-67224988	Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
22	nsv468604	chr11:67186000-67283891	Active TSS Strong transcription Bivalent/Poised TSS Weak transcription Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	132 gene(s)	inside rSNPs	diseases
23	nsv555256	chr11:67186000-67283891	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	132 gene(s)	inside rSNPs	diseases

mRNA abundance (count:20)

SNP	Gene	Cis/trans	Tissue	Source
rs869736	PTPRCAP	cis	Adipose Subcutaneous	GTEx
rs869736	ATG2A	cis	parietal	SCAN
rs869736	PTPRCAP	cis	Artery Tibial	GTEx
rs869736	RPS6KB2	cis	lymphoblastoid	seeQTL
rs869736	PTPRCAP	cis	Muscle Skeletal	GTEx
rs869736	RPS6KB2	cis	multi-tissue	Pritchard
rs869736	PTPRCAP	cis	Esophagus Muscularis	GTEx
rs869736	CDC42EP2	cis	parietal	SCAN
rs869736	PTPRCAP	cis	Skin Sun Exposed Lower leg	GTEx
rs869736	SYVN1	cis	parietal	SCAN
rs869736	AP003419.16	cis	Heart Left Ventricle	GTEx
rs869736	CORO1B	cis	cerebellum	SCAN
rs869736	PTPRCAP	cis	cerebellum	SCAN
rs869736	NDUFV1	cis	parietal	SCAN
rs869736	GSTP1	cis	parietal	SCAN
rs869736	PTPRCAP	cis	Nerve Tibial	GTEx
rs869736	RPS6KB2	cis	Lymphoblastoid	GTEx
rs869736	GSTP1	cis	cerebellum	SCAN
rs869736	PTPRCAP	cis	Heart Left Ventricle	GTEx
rs869736	PTPRCAP	cis	Thyroid	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:67196800-67210200	Weak transcription	Fetal Kidney	kidney
2	chr11:67197200-67206200	Strong transcription	Brain Cingulate Gyrus	brain
3	chr11:67197200-67206800	Weak transcription	Hela-S3	cervix
4	chr11:67197200-67206800	Weak transcription	NHDF-Ad	bronchial
5	chr11:67197200-67207000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr11:67197200-67207000	Weak transcription	Right Atrium	heart
7	chr11:67197200-67209400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr11:67197200-67209800	Weak transcription	Fetal Heart	heart
9	chr11:67197200-67210000	Strong transcription	Fetal Brain Female	brain
10	chr11:67197200-67210000	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr11:67197400-67206800	Strong transcription	Brain Hippocampus Middle	brain
12	chr11:67197400-67209400	Strong transcription	Fetal Intestine Large	intestine
13	chr11:67197600-67208200	Strong transcription	Brain Germinal Matrix	brain
14	chr11:67197600-67209400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr11:67198200-67206800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr11:67198200-67207000	Strong transcription	Brain Anterior Caudate	brain
17	chr11:67198200-67207000	Strong transcription	Brain Inferior Temporal Lobe	brain
18	chr11:67198200-67209600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr11:67198200-67209600	Strong transcription	Cortex derived primary cultured neurospheres	brain
20	chr11:67198200-67209800	Strong transcription	NHLF	lung
21	chr11:67198400-67207800	Strong transcription	Lung	lung
22	chr11:67198800-67207400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr11:67199400-67207000	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr11:67200600-67208800	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr11:67201000-67209800	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr11:67201200-67207600	Weak transcription	Fetal Lung	lung
27	chr11:67201200-67207600	Weak transcription	HUVEC	blood vessel
28	chr11:67201600-67210000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr11:67202000-67207200	Transcr. at gene 5' and 3'	Dnd41	blood
30	chr11:67202200-67206200	Transcr. at gene 5' and 3'	Primary hematopoietic stem cells short term culture	blood
31	chr11:67202200-67210200	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
32	chr11:67202400-67207000	Weak transcription	Osteobl	bone
33	chr11:67202400-67209800	Weak transcription	HepG2	liver
34	chr11:67202400-67210200	Weak transcription	Psoas Muscle	Psoas
35	chr11:67202800-67206200	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr11:67202800-67206600	Genic enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr11:67203000-67207600	Transcr. at gene 5' and 3'	Colonic Mucosa	Colon
38	chr11:67203200-67207000	Weak transcription	NHEK	skin
39	chr11:67203200-67210000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr11:67203200-67210400	Weak transcription	Ovary	ovary
41	chr11:67203400-67205600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr11:67203400-67206000	Transcr. at gene 5' and 3'	Sigmoid Colon	Sigmoid Colon
43	chr11:67203400-67206600	Active TSS	Rectal Smooth Muscle	rectum
44	chr11:67203600-67206000	Active TSS	Small Intestine	intestine
45	chr11:67203600-67206200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr11:67203600-67206600	Weak transcription	HSMMtube	muscle
47	chr11:67203600-67206800	Genic enhancers	H1 Cell Line	embryonic stem cell
48	chr11:67203600-67207000	Weak transcription	Brain Substantia Nigra	brain
49	chr11:67203600-67207000	Weak transcription	Colon Smooth Muscle	Colon
50	chr11:67203600-67208000	Weak transcription	Duodenum Smooth Muscle	Duodenum

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