Variant report

Variant	rs1638587
Chromosome Location	chr11:67177797-67177798
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	TAF1	chr11:67177339-67177926	H1-hESC	embryonic stem cell:	n/a	n/a
2	POLR2A	chr11:67176203-67178342	NB4	blood:	n/a	n/a
3	FOXA1	chr11:67177575-67177858	HepG2	liver:	n/a	n/a
4	POLR2A	chr11:67175796-67179861	HL-60	blood:	n/a	n/a
5	CTCF	chr11:67177731-67177806	K562	blood:	n/a	chr11:67177779-67177787
6	FOXA1	chr11:67177505-67177823	HepG2	liver:	n/a	n/a
7	ZBTB7A	chr11:67177323-67178143	ECC-1	luminal epithelium:	n/a	n/a
8	MTA3	chr11:67175100-67179965	GM12878	blood:	n/a	n/a
9	POLR2A	chr11:67176221-67179699	GM12891	blood:	n/a	n/a
10	STAT5A	chr11:67176054-67178296	GM12878	blood:	n/a	chr11:67176338-67176350 chr11:67176192-67176204 chr11:67177642-67177654 chr11:67176831-67176839 chr11:67177842-67177854
11	POLR2A	chr11:67176412-67178416	GM12878	blood:	n/a	n/a
12	POLR2A	chr11:67176537-67178308	GM12878	blood:	n/a	n/a
13	CTCF	chr11:67177753-67177837	MCF-7	breast:	n/a	chr11:67177779-67177787
14	CTCF	chr11:67177770-67177827	GM12891	blood:	n/a	chr11:67177779-67177787
15	POLR2A	chr11:67177422-67178432	GM15510	blood:	n/a	n/a
16	POLR2A	chr11:67177318-67178406	GM18505	blood:	n/a	n/a
17	CHD2	chr11:67177761-67177871	HepG2	liver:	n/a	n/a
18	ELF1	chr11:67176224-67177924	GM12878	blood:	n/a	n/a
19	POLR2A	chr11:67177165-67178698	GM12878	blood:	n/a	n/a
20	CTCF	chr11:67177700-67177850	GM12868	blood:	n/a	chr11:67177779-67177787
21	MYC	chr11:67176306-67177868	NB4	blood:	n/a	chr11:67176436-67176446 chr11:67177646-67177656
22	FOXA1	chr11:67177527-67177859	T-47D	breast:	n/a	n/a
23	POLR2A	chr11:67175692-67179867	GM12892	blood:	n/a	n/a
24	NFYB	chr11:67177579-67177878	Hela-S3	cervix:	n/a	n/a
25	POLR2A	chr11:67177743-67177856	Hela-S3	cervix:	n/a	n/a
26	CTCF	chr11:67177680-67177830	GM12872	blood:	n/a	chr11:67177779-67177787
27	CHD2	chr11:67177662-67177862	H1-hESC	embryonic stem cell:	n/a	n/a
28	POLR2A	chr11:67176168-67179252	HL-60	blood:	n/a	n/a
29	CTCF	chr11:67177700-67177850	HepG2	liver:	n/a	chr11:67177779-67177787
30	CTCF	chr11:67177700-67177850	GM06990	blood:	n/a	chr11:67177779-67177787
31	EBF1	chr11:67177644-67177877	GM12878	blood:	n/a	chr11:67177752-67177763
32	POLR2A	chr11:67177593-67178140	ECC-1	luminal epithelium:	n/a	n/a
33	POLR2A	chr11:67176013-67179736	GM12878	blood:	n/a	n/a
34	POLR2A	chr11:67177208-67178430	GM12878	blood:	n/a	n/a
35	POLR2A	chr11:67175740-67178488	GM12892	blood:	n/a	n/a
36	RFX5	chr11:67177796-67177804	H1-hESC	embryonic stem cell:	n/a	n/a
37	POLR2A	chr11:67177156-67178508	K562	blood:	n/a	n/a
38	CTCF	chr11:67177728-67177817	H1-hESC	embryonic stem cell:	n/a	chr11:67177779-67177787
39	NFYA	chr11:67177576-67177880	Hela-S3	cervix:	n/a	n/a
40	CTCF	chr11:67177762-67177820	MCF-7	breast:	n/a	chr11:67177779-67177787
41	SP1	chr11:67177436-67177909	H1-hESC	embryonic stem cell:	n/a	chr11:67177646-67177656 chr11:67177645-67177657 chr11:67177646-67177655 chr11:67177645-67177656 chr11:67177645-67177657 chr11:67177646-67177660 chr11:67177647-67177656
42	CTCF	chr11:67177734-67177828	MCF-7	breast:	n/a	chr11:67177779-67177787
43	MAX	chr11:67176286-67177860	NB4	blood:	n/a	chr11:67176436-67176446 chr11:67177646-67177656
44	POLR2A	chr11:67176293-67178650	GM12892	blood:	n/a	n/a
45	CTCF	chr11:67177706-67177838	Spleen_OC	spleen:	n/a	chr11:67177779-67177787
46	POLR2A	chr11:67176190-67179080	GM12892	blood:	n/a	n/a
47	POLR2A	chr11:67177767-67177856	MCF10A-Er-Src	breast:	n/a	n/a
48	CTCF	chr11:67177660-67177810	GM12869	blood:	n/a	chr11:67177779-67177787
49	CTCF	chr11:67177740-67177891	GM19239	blood:	n/a	chr11:67177779-67177787
50	POLR2A	chr11:67177284-67178205	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:67177350..67179552-chr11:67244883..67247528,2	K562	blood:
2	chr11:67176964..67178797-chr11:67202823..67204626,2	K562	blood:
3	chr11:67177049..67178732-chr17:56707856..56710336,2	MCF-7	breast:
4	chr11:67175789..67179239-chr11:67234277..67236634,3	MCF-7	breast:
5	chr11:67177386..67180366-chr17:57935264..57937336,3	MCF-7	breast:
6	chr11:67175949..67181191-chr11:67230601..67234346,6	K562	blood:
7	chr11:67176577..67178931-chr11:67250966..67253943,2	MCF-7	breast:

Variant related genes	Relation type
PPP1CA	TF binding region
CARNS1	TF binding region
ENSG00000255949	Chromatin interaction
ENSG00000172663	Chromatin interaction
ENSG00000212195	Chromatin interaction

Extended variants
information (count: 129 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:104)

rs_ID	r²[population]
rs10896175	1.00[EUR][1000 genomes]
rs11227796	1.00[EUR][1000 genomes]
rs11227804	1.00[EUR][1000 genomes]
rs12293606	1.00[EUR][1000 genomes]
rs1382089	1.00[EUR][1000 genomes]
rs1618605	1.00[EUR][1000 genomes]
rs1620333	1.00[EUR][1000 genomes]
rs1624189	1.00[EUR][1000 genomes]
rs1625032	1.00[EUR][1000 genomes]
rs1625892	1.00[EUR][1000 genomes]
rs1630068	1.00[EUR][1000 genomes]
rs1632616	1.00[EUR][1000 genomes]
rs1638558	1.00[EUR][1000 genomes]
rs1638559	1.00[EUR][1000 genomes]
rs1638560	1.00[EUR][1000 genomes]
rs1638561	1.00[EUR][1000 genomes]
rs1638562	1.00[EUR][1000 genomes]
rs1638563	1.00[EUR][1000 genomes]
rs1638570	1.00[EUR][1000 genomes]
rs1638572	1.00[EUR][1000 genomes]
rs1638575	1.00[EUR][1000 genomes]
rs1638576	1.00[EUR][1000 genomes]
rs1638577	1.00[EUR][1000 genomes]
rs1638581	1.00[EUR][1000 genomes]
rs1638584	1.00[EUR][1000 genomes]
rs1790729	1.00[EUR][1000 genomes]
rs1790730	1.00[EUR][1000 genomes]
rs1790734	1.00[EUR][1000 genomes]
rs1790736	1.00[EUR][1000 genomes]
rs1790741	1.00[EUR][1000 genomes]
rs1790743	1.00[EUR][1000 genomes]
rs1790744	1.00[EUR][1000 genomes]
rs1790745	1.00[EUR][1000 genomes]
rs1790749	1.00[MEX][hapmap];1.00[EUR][1000 genomes]
rs1790750	1.00[EUR][1000 genomes]
rs1790754	1.00[EUR][1000 genomes]
rs1790756	1.00[EUR][1000 genomes]
rs1790763	1.00[EUR][1000 genomes]
rs1790764	1.00[EUR][1000 genomes]
rs1790765	1.00[EUR][1000 genomes]
rs1824712	1.00[EUR][1000 genomes]
rs2511058	1.00[EUR][1000 genomes]
rs2511059	1.00[EUR][1000 genomes]
rs2514013	1.00[EUR][1000 genomes]
rs2514014	1.00[EUR][1000 genomes]
rs2514015	1.00[EUR][1000 genomes]
rs2514021	1.00[AMR][1000 genomes]
rs2514064	1.00[EUR][1000 genomes]
rs2514262	1.00[EUR][1000 genomes]
rs2514263	1.00[EUR][1000 genomes]
rs3016861	1.00[EUR][1000 genomes]
rs35363135	1.00[EUR][1000 genomes]
rs56050553	1.00[EUR][1000 genomes]
rs56102510	1.00[EUR][1000 genomes]
rs56173916	1.00[EUR][1000 genomes]
rs56405884	1.00[EUR][1000 genomes]
rs56973649	1.00[EUR][1000 genomes]
rs57047868	1.00[EUR][1000 genomes]
rs57748654	1.00[EUR][1000 genomes]
rs57749415	1.00[EUR][1000 genomes]
rs57757103	1.00[EUR][1000 genomes]
rs57955602	1.00[EUR][1000 genomes]
rs58999825	1.00[EUR][1000 genomes]
rs596431	1.00[EUR][1000 genomes]
rs596944	1.00[EUR][1000 genomes]
rs601363	1.00[EUR][1000 genomes]
rs60136955	1.00[EUR][1000 genomes]
rs60251934	1.00[EUR][1000 genomes]
rs602720	1.00[EUR][1000 genomes]
rs604540	1.00[EUR][1000 genomes]
rs60521870	1.00[EUR][1000 genomes]
rs60751057	1.00[EUR][1000 genomes]
rs611697	1.00[EUR][1000 genomes]
rs61282424	1.00[EUR][1000 genomes]
rs61429992	1.00[EUR][1000 genomes]
rs61610719	1.00[EUR][1000 genomes]
rs618633	1.00[EUR][1000 genomes]
rs641081	1.00[EUR][1000 genomes]
rs7104627	1.00[EUR][1000 genomes]
rs7121803	1.00[EUR][1000 genomes]
rs7124630	1.00[EUR][1000 genomes]
rs73490545	1.00[EUR][1000 genomes]
rs73490554	1.00[EUR][1000 genomes]
rs73501797	1.00[EUR][1000 genomes]
rs73501800	1.00[EUR][1000 genomes]
rs73503965	1.00[AMR][1000 genomes]
rs73506004	1.00[EUR][1000 genomes]
rs73506015	1.00[EUR][1000 genomes]
rs73506054	1.00[EUR][1000 genomes]
rs73506056	1.00[EUR][1000 genomes]
rs73506069	1.00[EUR][1000 genomes]
rs73506074	1.00[EUR][1000 genomes]
rs73508321	1.00[AMR][1000 genomes]
rs743679	1.00[EUR][1000 genomes]
rs7947114	1.00[EUR][1000 genomes]
rs8191436	1.00[EUR][1000 genomes]
rs8191446	1.00[EUR][1000 genomes]
rs8191449	1.00[EUR][1000 genomes]
rs949250	1.00[EUR][1000 genomes]
rs949251	1.00[EUR][1000 genomes]
rs949252	1.00[EUR][1000 genomes]
rs949253	1.00[EUR][1000 genomes]
rs949254	1.00[EUR][1000 genomes]
rs949255	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:25 , 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	nsv897796	chr11:67021518-67186000	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	103 gene(s)	inside rSNPs	diseases
3	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
4	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
5	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
6	nsv1047890	chr11:67058231-67184436	Flanking Active TSS Enhancers Strong transcription Genic enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
7	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
8	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
9	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
10	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
11	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
12	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
13	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
14	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
15	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
16	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
17	nsv516453	chr11:67164495-67186000	Genic enhancers Active TSS Flanking Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
18	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
19	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
20	nsv897810	chr11:67166310-67196237	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	54 gene(s)	inside rSNPs	diseases
21	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
22	nsv897812	chr11:67174597-67198887	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
23	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
24	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
25	nsv555255	chr11:67177797-67191449	Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:79 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:67169800-67177800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr11:67169800-67178000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr11:67170000-67182800	Weak transcription	Right Atrium	heart
4	chr11:67171600-67177800	Transcr. at gene 5' and 3'	Fetal Thymus	thymus
5	chr11:67172400-67177800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr11:67172400-67177800	Transcr. at gene 5' and 3'	Primary T cells fromperipheralblood	blood
7	chr11:67172400-67177800	Transcr. at gene 5' and 3'	Primary mononuclear cells fromperipheralblood	Blood
8	chr11:67172400-67178000	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
9	chr11:67172600-67177800	Weak transcription	K562	blood
10	chr11:67172600-67178400	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
11	chr11:67173800-67177800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
12	chr11:67173800-67177800	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
13	chr11:67173800-67178400	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
14	chr11:67173800-67181000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
15	chr11:67174000-67182200	Enhancers	Brain Hippocampus Middle	brain
16	chr11:67174200-67177800	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
17	chr11:67174200-67177800	Enhancers	Brain Substantia Nigra	brain
18	chr11:67174200-67181200	Enhancers	Brain Cingulate Gyrus	brain
19	chr11:67174400-67179200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
20	chr11:67174400-67181200	Enhancers	Brain Angular Gyrus	brain
21	chr11:67174400-67181400	Bivalent Enhancer	Fetal Muscle Leg	muscle
22	chr11:67175000-67178200	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
23	chr11:67175400-67177800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
24	chr11:67175400-67181200	Enhancers	Brain Anterior Caudate	brain
25	chr11:67175600-67177800	Enhancers	Primary monocytes fromperipheralblood	blood
26	chr11:67175800-67178400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr11:67175800-67178600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr11:67176000-67177800	Transcr. at gene 5' and 3'	Primary B cells from peripheral blood	blood
29	chr11:67176000-67178200	Flanking Active TSS	Primary T cells from cord blood	blood
30	chr11:67176000-67178200	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr11:67176200-67178400	Enhancers	Right Ventricle	heart
32	chr11:67176400-67177800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
33	chr11:67176400-67182400	Enhancers	Primary hematopoietic stem cells	blood
34	chr11:67176600-67178200	Enhancers	H1 Cell Line	embryonic stem cell
35	chr11:67176600-67178200	Enhancers	Primary B cells from cord blood	blood
36	chr11:67176600-67179000	Bivalent Enhancer	Placenta	Placenta
37	chr11:67176800-67178200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr11:67176800-67178200	Enhancers	Lung	lung
39	chr11:67177000-67178000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
40	chr11:67177000-67178200	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
41	chr11:67177000-67179200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr11:67177000-67179600	Weak transcription	Esophagus	oesophagus
43	chr11:67177000-67181200	Enhancers	Brain Inferior Temporal Lobe	brain
44	chr11:67177200-67177800	Transcr. at gene 5' and 3'	Primary Natural Killer cells fromperipheralblood	blood
45	chr11:67177200-67177800	Transcr. at gene 5' and 3'	Thymus	Thymus
46	chr11:67177200-67178000	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr11:67177200-67178000	Enhancers	iPS-20b Cell Line	embryonic stem cell
48	chr11:67177200-67178000	Enhancers	Fetal Intestine Small	intestine
49	chr11:67177200-67178200	Transcr. at gene 5' and 3'	Primary T regulatory cells fromperipheralblood	blood
50	chr11:67177200-67178400	Enhancers	Pancreas	Pancrea

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