Variant report

Variant	rs3741168
Chromosome Location	chr11:67235351-67235352
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:28)
CpG islands
(count:0)
Chromatin interactive
region (count:20)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:28 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ZBTB7A	chr11:67235223-67235433	K562	blood:	n/a	n/a
2	HCFC1	chr11:67235249-67237451	Hela-S3	cervix:	n/a	n/a
3	POLR2A	chr11:67233847-67235390	GM12878	blood:	n/a	n/a
4	MTA3	chr11:67235106-67237227	GM12878	blood:	n/a	n/a
5	POLR2A	chr11:67235026-67237150	HCT-116	colon:	n/a	n/a
6	POLR2A	chr11:67233795-67237091	K562	blood:	n/a	n/a
7	POLR2A	chr11:67234507-67237181	K562	blood:	n/a	n/a
8	POLR2A	chr11:67235152-67235423	U87	brain:	n/a	n/a
9	NFIC	chr11:67235303-67236085	ECC-1	luminal epithelium:	n/a	n/a
10	POLR2A	chr11:67235344-67237176	MCF-7	breast:	n/a	n/a
11	POLR2A	chr11:67233884-67237113	Hela-S3	cervix:	n/a	n/a
12	POLR2A	chr11:67235072-67235658	Hela-S3	cervix:	n/a	n/a
13	SIN3AK20	chr11:67235244-67237281	MCF-7	breast:	n/a	n/a
14	POLR2A	chr11:67233884-67237151	Raji	blood:	n/a	n/a
15	POLR2A	chr11:67234515-67237185	ECC-1	luminal epithelium:	n/a	n/a
16	ZBTB7A	chr11:67235342-67235939	ECC-1	luminal epithelium:	n/a	n/a
17	POLR2A	chr11:67234959-67236169	ECC-1	luminal epithelium:	n/a	n/a
18	POLR2A	chr11:67235197-67237121	GM12891	blood:	n/a	n/a
19	POLR2A	chr11:67235247-67237155	MCF10A-Er-Src	breast:	n/a	n/a
20	POLR2A	chr11:67235119-67235503	SK-N-SH	brain:	n/a	n/a
21	POLR2A	chr11:67235259-67237302	PANC-1	pancreas:	n/a	n/a
22	ZBTB7A	chr11:67235237-67235870	ECC-1	luminal epithelium:	n/a	n/a
23	POLR2A	chr11:67234765-67237160	MCF-7	breast:	n/a	n/a
24	TCF12	chr11:67235351-67236091	ECC-1	luminal epithelium:	n/a	chr11:67235484-67235494
25	POLR2A	chr11:67233698-67237165	HCT-116	colon:	n/a	n/a
26	POLR2A	chr11:67230966-67237458	HepG2	liver:	n/a	n/a
27	POLR2A	chr11:67235142-67237212	Hela-S3	cervix:	n/a	n/a
28	POLR2A	chr11:67234754-67237283	K562	blood:	n/a	n/a

No data

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:67226396..67229007-chr11:67234982..67237548,2	K562	blood:
2	chr11:67234712..67238016-chr11:67274176..67276331,3	K562	blood:
3	chr11:67232230..67238185-chr11:67272105..67277120,9	K562	blood:
4	chr11:67234942..67238660-chr11:67246245..67252394,7	MCF-7	breast:
5	chr11:67069155..67071597-chr11:67234852..67239277,5	MCF-7	breast:
6	chr11:67156700..67160978-chr11:67234255..67237148,8	MCF-7	breast:
7	chr11:67222064..67223632-chr11:67234422..67237101,2	K562	blood:
8	chr11:67231244..67235869-chr11:67255079..67259378,6	MCF-7	breast:
9	chr11:67215208..67219901-chr11:67230573..67236211,5	K562	blood:
10	chr11:67137032..67142528-chr11:67234580..67238729,6	MCF-7	breast:
11	chr11:67234460..67237754-chr11:67271882..67275850,7	MCF-7	breast:
12	chr11:67201248..67204152-chr11:67232413..67236121,3	K562	blood:
13	chr11:67164667..67170931-chr11:67232207..67238345,15	MCF-7	breast:
14	chr11:67230107..67238941-chr11:67268499..67277838,23	MCF-7	breast:
15	chr11:67181921..67184734-chr11:67234626..67236825,2	K562	blood:
16	chr11:67175789..67179239-chr11:67234277..67236634,3	MCF-7	breast:
17	chr11:67166766..67171737-chr11:67231413..67236466,7	K562	blood:
18	chr11:67056211..67059053-chr11:67235087..67237043,2	MCF-7	breast:
19	chr11:67229962..67234772-chr11:67234827..67242516,28	K562	blood:
20	chr11:66383175..66385697-chr11:67233661..67236166,2	MCF-7	breast:

No data

Variant related genes	Relation type
TMEM134	TF binding region
ENSG00000239306	Chromatin interaction
ENSG00000172932	Chromatin interaction
ENSG00000255949	Chromatin interaction
ENSG00000269913	Chromatin interaction
ENSG00000175463	Chromatin interaction
ENSG00000175505	Chromatin interaction
ENSG00000172830	Chromatin interaction
ENSG00000172663	Chromatin interaction
ENSG00000172508	Chromatin interaction
ENSG00000172613	Chromatin interaction
ENSG00000167797	Chromatin interaction
ENSG00000175544	Chromatin interaction
ENSG00000248643	Chromatin interaction
ENSG00000110711	Chromatin interaction
ENSG00000256514	Chromatin interaction
ENSG00000110697	Chromatin interaction
ENSG00000172531	Chromatin interaction

Extended variants
information (count: 65 )
Associated
traits (count: 21 )

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10274	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[CHD][hapmap];0.94[GIH][hapmap];0.94[JPT][hapmap];0.91[MEX][hapmap];0.98[TSI][hapmap];0.80[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11227793	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11601325	0.89[CEU][hapmap];0.88[GIH][hapmap];0.91[MEX][hapmap];0.95[TSI][hapmap];0.89[EUR][1000 genomes]
rs12288107	0.82[CHD][hapmap];0.84[YRI][hapmap]
rs12290164	0.82[CHD][hapmap];0.84[YRI][hapmap]
rs12573992	0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12787021	0.89[ASW][hapmap];1.00[CEU][hapmap];0.80[CHD][hapmap];0.94[GIH][hapmap];1.00[LWK][hapmap];0.96[MEX][hapmap];0.93[MKK][hapmap];0.98[TSI][hapmap];0.84[YRI][hapmap];0.93[AFR][1000 genomes];0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12799746	0.80[EUR][1000 genomes]
rs13859	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1476792	1.00[ASW][hapmap];1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[CHD][hapmap];0.94[GIH][hapmap];0.94[JPT][hapmap];0.96[MEX][hapmap];0.84[MKK][hapmap];0.98[TSI][hapmap];0.84[YRI][hapmap];0.80[AFR][1000 genomes];0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1626067	1.00[ASW][hapmap];0.84[YRI][hapmap]
rs1628442	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1638555	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1638556	1.00[ASW][hapmap];1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[CHD][hapmap];0.94[GIH][hapmap];0.94[JPT][hapmap];0.96[LWK][hapmap];1.00[MEX][hapmap];0.93[MKK][hapmap];0.98[TSI][hapmap];0.84[YRI][hapmap];0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1638557	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1638565	0.87[AFR][1000 genomes];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1638588	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];0.89[MKK][hapmap];0.98[TSI][hapmap];0.84[YRI][hapmap];0.95[AFR][1000 genomes];0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1790733	0.80[CHD][hapmap];0.84[YRI][hapmap]
rs1790747	0.84[YRI][hapmap]
rs1790752	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[CHD][hapmap];0.88[GIH][hapmap];0.94[JPT][hapmap];0.96[MEX][hapmap];0.98[TSI][hapmap];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1790753	1.00[CEU][hapmap];0.94[CHB][hapmap];0.94[JPT][hapmap];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1790761	1.00[CEU][hapmap];0.94[CHB][hapmap];0.94[JPT][hapmap];0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1808279	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1893973	0.87[EUR][1000 genomes]
rs2109123	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2276118	0.89[CHB][hapmap];0.89[JPT][hapmap];0.93[TSI][hapmap]
rs2302264	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[CHD][hapmap];0.94[GIH][hapmap];0.88[JPT][hapmap];0.91[MEX][hapmap];0.98[TSI][hapmap];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs35787427	0.88[EUR][1000 genomes]
rs36089024	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4084113	0.81[CEU][hapmap];0.91[MEX][hapmap];0.91[TSI][hapmap]
rs4465371	0.86[TSI][hapmap]
rs4930427	1.00[CEU][hapmap];0.94[CHB][hapmap];0.94[JPT][hapmap];0.80[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs595130	0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs61889868	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs630172	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7110021	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7114510	0.89[CEU][hapmap];0.88[GIH][hapmap];0.91[MEX][hapmap];0.95[TSI][hapmap];0.89[EUR][1000 genomes]
rs7131041	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7479801	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[CHD][hapmap];0.94[GIH][hapmap];0.94[JPT][hapmap];1.00[MEX][hapmap];0.98[TSI][hapmap];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs869736	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]
rs872375	0.80[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs917570	0.81[CEU][hapmap];0.81[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	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
7	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
8	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
9	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
10	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
11	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
12	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
13	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
14	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
15	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
16	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
17	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
18	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
19	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
20	nsv527056	chr11:67207426-67294308	Genic enhancers Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS 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	115 gene(s)	inside rSNPs	diseases
21	esv1813337	chr11:67217703-67235815	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
22	nsv983155	chr11:67220251-67251432	Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	56 gene(s)	inside rSNPs	diseases
23	esv2422195	chr11:67234322-67626901	Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Active TSS Weak transcription 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	146 gene(s)	inside rSNPs	diseases

mRNA abundance (count:21)

SNP	Gene	Cis/trans	Tissue	Source
rs3741168	PTPRCAP	cis	Esophagus Muscularis	GTEx
rs3741168	PTPRCAP	cis	Skin Sun Exposed Lower leg	GTEx
rs3741168	RPS6KB2	cis	Lymphoblastoid	GTEx
rs3741168	PTPRCAP	cis	cerebellum	SCAN
rs3741168	PTPRCAP	cis	Heart Left Ventricle	GTEx
rs3741168	RPS6KB2	cis	lymphoblastoid	seeQTL
rs3741168	ATG2A	cis	parietal	SCAN
rs3741168	PTPRCAP	cis	Adipose Subcutaneous	GTEx
rs3741168	PTPRCAP	cis	Nerve Tibial	GTEx
rs3741168	NDUFV1	cis	parietal	SCAN
rs3741168	PTPRCAP	cis	Thyroid	GTEx
rs3741168	SYVN1	cis	parietal	SCAN
rs3741168	CDC42EP2	cis	parietal	SCAN
rs3741168	GSTP1	cis	parietal	SCAN
rs3741168	PTPRCAP	cis	Muscle Skeletal	GTEx
rs3741168	PTPRCAP	cis	Artery Tibial	GTEx
rs3741168	AP003419.16	cis	Heart Left Ventricle	GTEx
rs3741168	NRXN2	cis	cerebellum	SCAN
rs3741168	GSTP1	cis	cerebellum	SCAN
rs3741168	CORO1B	cis	cerebellum	SCAN
rs3741168	RPS6KB2	cis	multi-tissue	Pritchard

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:67232600-67235600	Weak transcription	Ovary	ovary
2	chr11:67232800-67235800	Weak transcription	Aorta	Aorta
3	chr11:67233000-67235400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr11:67233000-67235400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr11:67233000-67235400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
6	chr11:67233000-67235400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
7	chr11:67233000-67235400	Weak transcription	Pancreatic Islets	Pancreatic Islet
8	chr11:67233000-67235400	Weak transcription	Psoas Muscle	Psoas
9	chr11:67233000-67235400	Weak transcription	Small Intestine	intestine
10	chr11:67233000-67235400	Weak transcription	HSMM	muscle
11	chr11:67233000-67235400	Weak transcription	NHDF-Ad	bronchial
12	chr11:67233000-67235600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr11:67233000-67235600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr11:67233000-67235600	Weak transcription	Left Ventricle	heart
15	chr11:67233000-67235600	Weak transcription	HUVEC	blood vessel
16	chr11:67233000-67235800	Weak transcription	Fetal Kidney	kidney
17	chr11:67233200-67235400	Weak transcription	HUES48 Cell Line	embryonic stem cell
18	chr11:67233200-67235400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
19	chr11:67233200-67235400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr11:67233200-67235400	Genic enhancers	Fetal Intestine Small	intestine
21	chr11:67233200-67235400	Weak transcription	Rectal Smooth Muscle	rectum
22	chr11:67233200-67235400	Weak transcription	NH-A	brain
23	chr11:67233200-67235600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr11:67233200-67235600	Weak transcription	H9 Cell Line	embryonic stem cell
25	chr11:67233200-67235600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr11:67233200-67235600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
27	chr11:67233200-67235600	Weak transcription	Primary monocytes fromperipheralblood	blood
28	chr11:67233200-67235600	Enhancers	Primary hematopoietic stem cells short term culture	blood
29	chr11:67233200-67235600	Enhancers	Primary T helper cells PMA-I stimulated	--
30	chr11:67233200-67235600	Weak transcription	K562	blood
31	chr11:67233200-67235800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr11:67233200-67235800	Enhancers	Primary T helper naive cells from peripheral blood	blood
33	chr11:67233400-67235600	Weak transcription	Primary neutrophils fromperipheralblood	blood
34	chr11:67233800-67235400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
35	chr11:67233800-67235400	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
36	chr11:67233800-67235400	Genic enhancers	Placenta	Placenta
37	chr11:67233800-67235400	Enhancers	GM12878-XiMat	blood
38	chr11:67233800-67235600	Genic enhancers	Cortex derived primary cultured neurospheres	brain
39	chr11:67233800-67236000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
40	chr11:67234000-67236000	Enhancers	Spleen	Spleen
41	chr11:67234000-67236600	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr11:67234200-67235400	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr11:67234200-67235400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr11:67234200-67235400	Enhancers	Primary T cells from cord blood	blood
45	chr11:67234200-67235400	Enhancers	Stomach Mucosa	stomach
46	chr11:67234200-67235800	Enhancers	Primary T killer memory cells from peripheral blood	blood
47	chr11:67234200-67235800	Enhancers	Fetal Lung	lung
48	chr11:67234200-67237200	Active TSS	iPS-15b Cell Line	embryonic stem cell
49	chr11:67234400-67235400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr11:67234400-67235400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood

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