Variant report

Variant	rs650012
Chromosome Location	chr11:64071693-64071694
allele	A/C
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	chr11:64071691-64074716	K562	blood:	n/a	n/a
2	SMC3	chr11:64071459-64073084	SK-N-SH	brain:	n/a	chr11:64071949-64071963 chr11:64072953-64072963 chr11:64071949-64071959 chr11:64072793-64072803
3	POLR2A	chr11:64071678-64072660	GM12891	blood:	n/a	n/a
4	PAX5	chr11:64071668-64072472	GM12878	blood:	n/a	n/a
5	RAD21	chr11:64071662-64072173	A549	lung:	n/a	chr11:64071998-64072010 chr11:64071949-64071959 chr11:64071949-64071963 chr11:64071947-64071959 chr11:64071945-64071964 chr11:64071948-64071961
6	POLR2A	chr11:64071688-64073210	ECC-1	luminal epithelium:	n/a	n/a
7	CREB1	chr11:64071691-64072514	H1-hESC	embryonic stem cell:	n/a	n/a
8	RAD21	chr11:64071690-64072170	ECC-1	luminal epithelium:	n/a	chr11:64071998-64072010 chr11:64071949-64071959 chr11:64071949-64071963 chr11:64071947-64071959 chr11:64071945-64071964 chr11:64071948-64071961
9	RAD21	chr11:64071636-64072278	MCF-7	breast:	n/a	chr11:64071998-64072010 chr11:64071949-64071959 chr11:64071949-64071963 chr11:64071947-64071959 chr11:64071945-64071964 chr11:64071948-64071961
10	RAD21	chr11:64071663-64072149	MCF-7	breast:	n/a	chr11:64071998-64072010 chr11:64071949-64071959 chr11:64071949-64071963 chr11:64071947-64071959 chr11:64071945-64071964 chr11:64071948-64071961
11	ZC3H11A	chr11:64071597-64072380	K562	blood:	n/a	n/a
12	SP4	chr11:64071690-64072532	H1-hESC	embryonic stem cell:	n/a	chr11:64072285-64072301
13	STAT5A	chr11:64071513-64072614	GM12878	blood:	n/a	chr11:64072289-64072301 chr11:64071926-64071940
14	POLR2A	chr11:64071693-64072191	H1-neurons	neurons:	n/a	n/a
15	BCL3	chr11:64071578-64072408	A549	lung:	n/a	n/a
16	HCFC1	chr11:64071097-64074523	Hela-S3	cervix:	n/a	n/a
17	REST	chr11:64071560-64072495	A549	lung:	n/a	n/a
18	POLR2A	chr11:64071638-64074206	GM12878	blood:	n/a	n/a
19	MAX	chr11:64071687-64074118	NB4	blood:	n/a	chr11:64072280-64072289 chr11:64073577-64073587 chr11:64073576-64073591 chr11:64072279-64072290 chr11:64072281-64072288 chr11:64073578-64073587 chr11:64072280-64072290 chr11:64073577-64073586 chr11:64073578-64073588 chr11:64073580-64073589 chr11:64072280-64072289
20	POLR2A	chr11:64071465-64075532	K562	blood:	n/a	n/a
21	POLR2A	chr11:64071613-64072794	K562	blood:	n/a	n/a
22	POLR2A	chr11:64071636-64073198	PFSK-1	brain:	n/a	n/a
23	POLR2A	chr11:64071691-64072776	GM12878	blood:	n/a	n/a
24	MAX	chr11:64071575-64074336	A549	lung:	n/a	chr11:64072280-64072289 chr11:64073577-64073587 chr11:64073576-64073591 chr11:64072279-64072290 chr11:64072281-64072288 chr11:64073578-64073587 chr11:64072280-64072290 chr11:64073577-64073586 chr11:64073578-64073588 chr11:64073580-64073589 chr11:64072280-64072289
25	TEAD4	chr11:64071566-64072786	K562	blood:	n/a	n/a
26	MAX	chr11:64071686-64074279	MCF-7	breast:	n/a	chr11:64072280-64072289 chr11:64073577-64073587 chr11:64073576-64073591 chr11:64072279-64072290 chr11:64072281-64072288 chr11:64073578-64073587 chr11:64072280-64072290 chr11:64073577-64073586 chr11:64073578-64073588 chr11:64073580-64073589 chr11:64072280-64072289
27	POLR2A	chr11:64071636-64072775	GM12878	blood:	n/a	n/a
28	SP1	chr11:64071672-64073224	GM12878	blood:	n/a	chr11:64072950-64072960 chr11:64072700-64072712 chr11:64072780-64072792 chr11:64072880-64072889 chr11:64072950-64072959 chr11:64072837-64072849 chr11:64072951-64072960 chr11:64072837-64072849 chr11:64072700-64072712 chr11:64072982-64072992 chr11:64072702-64072711 chr11:64072951-64072964 chr11:64072981-64072993 chr11:64072287-64072299 chr11:64072949-64072961 chr11:64072566-64072578 chr11:64072983-64072992 chr11:64072781-64072791 chr11:64072839-64072848 chr11:64072781-64072790 chr11:64072759-64072771 chr11:64072567-64072576 chr11:64072981-64072993 chr11:64072950-64072960 chr11:64072288-64072302 chr11:64071997-64072011 chr11:64072949-64072961 chr11:64072288-64072297 chr11:64072287-64072299 chr11:64072982-64072992 chr11:64072566-64072578 chr11:64072950-64072964 chr11:64072701-64072710 chr11:64072879-64072891 chr11:64072781-64072791 chr11:64072782-64072791 chr11:64072879-64072891 chr11:64072761-64072770 chr11:64072780-64072792 chr11:64072982-64072991 chr11:64072701-64072715 chr11:64072760-64072774 chr11:64072513-64072527 chr11:64072781-64072790 chr11:64072950-64072959 chr11:64072781-64072795 chr11:64072857-64072869
29	POLR2A	chr11:64071681-64072841	U87	brain:	n/a	n/a
30	HEY1	chr11:64071652-64072723	K562	blood:	n/a	n/a
31	POLR2A	chr11:64071316-64073205	SK-N-MC	brain:	n/a	n/a
32	POLR2A	chr11:64071470-64074232	Raji	blood:	n/a	n/a
33	POLR2A	chr11:64071681-64072620	GM12892	blood:	n/a	n/a
34	POLR2A	chr11:64071690-64072789	Hela-S3	cervix:	n/a	n/a
35	CREB1	chr11:64071686-64073153	H1-hESC	embryonic stem cell:	n/a	n/a
36	POLR2A	chr11:64071652-64073251	GM12878	blood:	n/a	n/a
37	MAX	chr11:64071649-64072895	ECC-1	luminal epithelium:	n/a	chr11:64072280-64072289 chr11:64072279-64072290 chr11:64072281-64072288 chr11:64072280-64072290 chr11:64072280-64072289
38	POLR2A	chr11:64071681-64072804	GM12892	blood:	n/a	n/a
39	SIN3AK20	chr11:64071678-64072255	A549	lung:	n/a	n/a
40	POLR2A	chr11:64071492-64074705	K562	blood:	n/a	n/a
41	RAD21	chr11:64071691-64072259	H1-hESC	embryonic stem cell:	n/a	chr11:64071998-64072010 chr11:64071949-64071959 chr11:64071949-64071963 chr11:64071947-64071959 chr11:64071945-64071964 chr11:64071948-64071961
42	FOXM1	chr11:64071626-64072491	GM12878	blood:	n/a	n/a
43	BACH1	chr11:64071651-64072844	H1-hESC	embryonic stem cell:	n/a	n/a
44	CREB1	chr11:64071570-64073156	K562	blood:	n/a	n/a
45	CREB1	chr11:64071665-64073258	GM12878	blood:	n/a	n/a
46	RUNX3	chr11:64071650-64072855	GM12878	blood:	n/a	n/a
47	CBX3	chr11:64071689-64072868	K562	blood:	n/a	n/a
48	CTCF	chr11:64071690-64072112	T-47D	breast:	n/a	chr11:64071950-64071960 chr11:64071953-64071962 chr11:64071947-64071965 chr11:64071948-64071964 chr11:64071942-64071963 chr11:64071949-64071962 chr11:64071949-64071962
49	POLR2A	chr11:64071582-64074239	GM19193	blood:	n/a	n/a
50	CTCF	chr11:64071603-64072485	HCT-116	colon:	n/a	chr11:64071950-64071960 chr11:64071953-64071962 chr11:64071947-64071965 chr11:64071948-64071964 chr11:64071942-64071963 chr11:64071949-64071962 chr11:64071949-64071962

No.	Distal block	Cell Line	Cell type
1	chr11:64068655..64075946-chr11:64105786..64111623,11	K562	blood:
2	chr11:64070986..64076286-chr11:64124810..64128616,7	K562	blood:
3	chr11:64033188..64045448-chr11:64059274..64075790,38	MCF-7	breast:
4	chr11:63997014..63999742-chr11:64070693..64073511,5	MCF-7	breast:
5	chr11:63535885..63536509-chr11:64071588..64072193,2	K562	blood:
6	chr11:64052533..64053108-chr11:64071541..64072443,2	K562	blood:
7	chr11:64071328..64072338-chr11:64111400..64111928,3	MCF-7	breast:
8	chr11:64003628..64022712-chr11:64064086..64078429,56	MCF-7	breast:
9	chr11:64070411..64072227-chr11:64108642..64111595,2	MCF-7	breast:
10	chr11:63990938..63995618-chr11:64068467..64075569,11	MCF-7	breast:
11	chr11:64071691..64076218-chr11:64119080..64123328,5	MCF-7	breast:
12	chr11:64071470..64071981-chr11:64122658..64123242,2	MCF-7	breast:
13	chr11:64070461..64072737-chr2:174827568..174830464,2	K562	blood:
14	chr11:64070250..64072559-chr11:64125217..64126731,2	MCF-7	breast:
15	chr11:64071519..64072480-chr3:52444484..52444992,2	NB4	blood:
16	chr11:63997990..64000103-chr11:64070945..64073334,3	MCF-7	breast:
17	chr11:64062581..64067286-chr11:64069885..64074549,10	MCF-7	breast:
18	chr11:63973802..63976476-chr11:64070377..64073257,2	MCF-7	breast:
19	chr11:64038921..64039477-chr11:64071498..64072466,3	MCF-7	breast:
20	chr11:64069494..64072253-chr11:64119496..64122184,3	MCF-7	breast:
21	chr11:64012813..64019826-chr11:64070484..64074683,9	MCF-7	breast:
22	chr11:63971732..63972680-chr11:64071516..64072440,6	MCF-7	breast:
23	chr11:64066836..64070235-chr11:64070747..64073935,5	MCF-7	breast:
24	chr11:64069665..64072267-chr11:64127421..64129255,2	MCF-7	breast:
25	chr11:64034991..64040375-chr11:64070988..64074526,14	MCF-7	breast:
26	chr11:63950774..63958537-chr11:64070493..64074690,13	MCF-7	breast:
27	chr11:64005251..64012775-chr11:64065543..64076594,19	MCF-7	breast:

Variant related genes	Relation type
ESRRA	TF binding region
ENSG00000010318	Chromatin interaction
ENSG00000149782	Chromatin interaction
ENSG00000168439	Chromatin interaction
ENSG00000149781	Chromatin interaction
ENSG00000256940	Chromatin interaction
ENSG00000149743	Chromatin interaction
ENSG00000110011	Chromatin interaction
ENSG00000149761	Chromatin interaction
ENSG00000173486	Chromatin interaction
ENSG00000162302	Chromatin interaction
ENSG00000168071	Chromatin interaction
ENSG00000182450	Chromatin interaction
ENSG00000002330	Chromatin interaction
ENSG00000219435	Chromatin interaction
ENSG00000173457	Chromatin interaction
ENSG00000173264	Chromatin interaction
ENSG00000172845	Chromatin interaction
ENSG00000173511	Chromatin interaction
ENSG00000207024	Chromatin interaction
ENSG00000257086	Chromatin interaction
ENSG00000255651	Chromatin interaction

Extended variants
information (count: 29 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs505626	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs655896	0.90[LWK][hapmap]

Variant overlapped rSNPs/rCNVs (count:27 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv897631	chr11:63664882-64129722	Flanking Active TSS Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer 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	254 gene(s)	inside rSNPs	diseases
2	esv1802079	chr11:63746066-64151373	Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	247 gene(s)	inside rSNPs	diseases
3	nsv897646	chr11:63754986-64150370	Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	245 gene(s)	inside rSNPs	diseases
4	nsv1035875	chr11:63800238-64132030	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	234 gene(s)	inside rSNPs	diseases
5	nsv469961	chr11:63822940-64085967	Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	224 gene(s)	inside rSNPs	diseases
6	nsv897660	chr11:63860826-64125142	Weak transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription 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	231 gene(s)	inside rSNPs	diseases
7	nsv897661	chr11:63863405-64129722	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	233 gene(s)	inside rSNPs	diseases
8	nsv897662	chr11:63889749-64150370	Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	237 gene(s)	inside rSNPs	diseases
9	nsv897664	chr11:63919742-64150370	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh 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	237 gene(s)	inside rSNPs	diseases
10	nsv869944	chr11:63932152-64123062	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	227 gene(s)	inside rSNPs	diseases
11	nsv468593	chr11:63941734-64089874	Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Genic enhancers Strong transcription Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	212 gene(s)	inside rSNPs	diseases
12	nsv555185	chr11:63941734-64089874	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription 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	212 gene(s)	inside rSNPs	diseases
13	nsv555186	chr11:63949095-64097233	Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	212 gene(s)	inside rSNPs	diseases
14	nsv897667	chr11:63964657-64078380	Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	141 gene(s)	inside rSNPs	diseases
15	nsv897668	chr11:63964657-64085298	Weak transcription Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	163 gene(s)	inside rSNPs	diseases
16	nsv897669	chr11:63964657-64089874	Genic enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	164 gene(s)	inside rSNPs	diseases
17	nsv897670	chr11:63964657-64097233	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	164 gene(s)	inside rSNPs	diseases
18	nsv897671	chr11:63964657-64150370	Active TSS Flanking Active TSS Genic enhancers Weak transcription Enhancers Strong transcription Bivalent Enhancer 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 miRNA target site	179 gene(s)	inside rSNPs	diseases
19	nsv832186	chr11:63972260-64170059	Active TSS Genic enhancers Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	180 gene(s)	inside rSNPs	diseases
20	nsv897672	chr11:63979643-64082807	Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Weak transcription Strong transcription Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	140 gene(s)	inside rSNPs	diseases
21	esv1802320	chr11:63987425-64154633	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	178 gene(s)	inside rSNPs	diseases
22	nsv897679	chr11:63994692-64150370	Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	169 gene(s)	inside rSNPs	diseases
23	nsv897682	chr11:63999529-64170500	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	164 gene(s)	inside rSNPs	diseases
24	nsv1043277	chr11:64002997-64132030	Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
25	nsv897685	chr11:64048912-64150370	Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	102 gene(s)	inside rSNPs	diseases
26	nsv897686	chr11:64049021-64072244	Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
27	nsv897687	chr11:64049021-64078380	Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	59 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs650012	CXCL14	trans	lymphoblastoid	seeQTL

Chromatin state (count:121 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:64067600-64072000	Weak transcription	Aorta	Aorta
2	chr11:64068800-64071800	Weak transcription	HSMMtube	muscle
3	chr11:64070600-64071800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
4	chr11:64070800-64071800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
5	chr11:64070800-64071800	Enhancers	Fetal Heart	heart
6	chr11:64071200-64071800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr11:64071200-64071800	Enhancers	Primary B cells from cord blood	blood
8	chr11:64071200-64071800	Enhancers	Primary B cells from peripheral blood	blood
9	chr11:64071200-64071800	Enhancers	Primary hematopoietic stem cells	blood
10	chr11:64071200-64071800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
11	chr11:64071200-64071800	Enhancers	Fetal Intestine Small	intestine
12	chr11:64071200-64071800	Enhancers	Placenta	Placenta
13	chr11:64071200-64071800	Enhancers	Stomach Mucosa	stomach
14	chr11:64071200-64072000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr11:64071200-64072000	Flanking Active TSS	HepG2	liver
16	chr11:64071200-64072200	Flanking Active TSS	Hela-S3	cervix
17	chr11:64071200-64072400	Flanking Active TSS	Stomach Smooth Muscle	stomach
18	chr11:64071200-64072400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
19	chr11:64071200-64073000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr11:64071400-64071800	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr11:64071400-64071800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr11:64071400-64071800	Enhancers	Primary T cells from cord blood	blood
23	chr11:64071400-64071800	Enhancers	Primary T helper naive cells from peripheral blood	blood
24	chr11:64071400-64071800	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
25	chr11:64071400-64071800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
26	chr11:64071400-64071800	Enhancers	Cortex derived primary cultured neurospheres	brain
27	chr11:64071400-64071800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr11:64071400-64071800	Enhancers	Fetal Muscle Trunk	muscle
29	chr11:64071400-64071800	Enhancers	Fetal Muscle Leg	muscle
30	chr11:64071400-64071800	Enhancers	Fetal Thymus	thymus
31	chr11:64071400-64071800	Enhancers	Pancreas	Pancrea
32	chr11:64071400-64071800	Genic enhancers	Right Atrium	heart
33	chr11:64071400-64071800	Enhancers	NHEK	skin
34	chr11:64071400-64072000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
35	chr11:64071400-64072000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
36	chr11:64071400-64072000	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
37	chr11:64071400-64072000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr11:64071400-64072000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr11:64071400-64072000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr11:64071400-64072000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
41	chr11:64071400-64072000	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
42	chr11:64071400-64072000	Enhancers	Gastric	stomach
43	chr11:64071400-64072000	Flanking Active TSS	Rectal Smooth Muscle	rectum
44	chr11:64071400-64072000	Flanking Active TSS	Right Ventricle	heart
45	chr11:64071400-64072000	Enhancers	Sigmoid Colon	Sigmoid Colon
46	chr11:64071400-64072000	Flanking Active TSS	Spleen	Spleen
47	chr11:64071400-64072000	Flanking Active TSS	GM12878-XiMat	blood
48	chr11:64071400-64072000	Flanking Active TSS	K562	blood
49	chr11:64071400-64072400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
50	chr11:64071400-64072400	Flanking Active TSS	Colonic Mucosa	Colon

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