Variant report

Variant	rs2286614
Chromosome Location	chr11:64068310-64068311
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	REST	chr11:64068046-64068412	GM12878	blood:	n/a	n/a
2	CTCF	chr11:64068197-64068852	IMR90	lung:	n/a	chr11:64068631-64068649 chr11:64068633-64068646 chr11:64068632-64068648
3	RAD21	chr11:64067835-64069007	HCT-116	colon:	n/a	chr11:64068629-64068648
4	REST	chr11:64068008-64068706	PANC-1	pancreas:	n/a	n/a
5	POLR2A	chr11:64067567-64068958	H1-neurons	neurons:	n/a	n/a
6	CTCF	chr11:64067820-64068953	A549	lung:	n/a	chr11:64068631-64068649 chr11:64068633-64068646 chr11:64068632-64068648
7	MAX	chr11:64067917-64068872	HepG2	liver:	n/a	n/a
8	BHLHE40	chr11:64068137-64068754	K562	blood:	n/a	n/a
9	CCNT2	chr11:64068245-64068623	K562	blood:	n/a	n/a
10	CTCF	chr11:64067969-64068857	K562	blood:	n/a	chr11:64068631-64068649 chr11:64068633-64068646 chr11:64068632-64068648
11	UBTF	chr11:64068082-64068772	K562	blood:	n/a	n/a
12	REST	chr11:64068098-64068339	HepG2	liver:	n/a	n/a
13	ZNF143	chr11:64068114-64068810	H1-hESC	embryonic stem cell:	n/a	n/a
14	REST	chr11:64067930-64068631	ECC-1	luminal epithelium:	n/a	n/a
15	CTCF	chr11:64068220-64068370	GM12871	blood:	n/a	n/a
16	MAX	chr11:64068046-64068818	K562	blood:	n/a	n/a
17	REST	chr11:64067984-64068477	PANC-1	pancreas:	n/a	n/a
18	REST	chr11:64067964-64068721	A549	lung:	n/a	n/a
19	CTCF	chr11:64068236-64068924	HCT-116	colon:	n/a	chr11:64068631-64068649 chr11:64068633-64068646 chr11:64068632-64068648
20	TCF12	chr11:64067905-64069022	A549	lung:	n/a	n/a
21	E2F6	chr11:64067864-64068883	A549	lung:	n/a	n/a
22	REST	chr11:64068115-64068334	HepG2	liver:	n/a	n/a
23	BCL3	chr11:64067971-64068729	A549	lung:	n/a	n/a
24	MAX	chr11:64068217-64068722	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr11:64068200-64068350	BE2_C	brain:	n/a	n/a
26	POLR2A	chr11:64068206-64068864	K562	blood:	n/a	n/a
27	REST	chr11:64068091-64068402	K562	blood:	n/a	n/a
28	REST	chr11:64068034-64068377	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr11:64068011-64068796	GM12892	blood:	n/a	chr11:64068631-64068649 chr11:64068633-64068646 chr11:64068632-64068648
30	SIN3AK20	chr11:64067959-64068841	PANC-1	pancreas:	n/a	n/a
31	REST	chr11:64068010-64068439	HepG2	liver:	n/a	n/a
32	CTCF	chr11:64068013-64068809	GM19238	blood:	n/a	chr11:64068631-64068649 chr11:64068633-64068646 chr11:64068632-64068648
33	MAX	chr11:64068128-64068852	A549	lung:	n/a	n/a
34	POLR2A	chr11:64068027-64068910	PANC-1	pancreas:	n/a	n/a
35	GABPA	chr11:64067883-64068400	H1-hESC	embryonic stem cell:	n/a	n/a
36	USF1	chr11:64068281-64068799	A549	lung:	n/a	n/a
37	REST	chr11:64068055-64068400	SK-N-SH	brain:	n/a	n/a
38	REST	chr11:64068031-64068380	PFSK-1	brain:	n/a	n/a
39	POLR2A	chr11:64068002-64068905	H1-neurons	neurons:	n/a	n/a
40	CTCF	chr11:64067986-64068848	GM12878	blood:	n/a	chr11:64068631-64068649 chr11:64068633-64068646 chr11:64068632-64068648
41	CTCF	chr11:64068027-64068789	GM19240	blood:	n/a	chr11:64068631-64068649 chr11:64068633-64068646 chr11:64068632-64068648
42	GTF3C2	chr11:64068067-64069262	K562	blood:	n/a	n/a
43	RCOR1	chr11:64067945-64068921	IMR90	lung:	n/a	n/a
44	SUZ12	chr11:64066782-64068589	H1-hESC	embryonic stem cell:	n/a	n/a
45	MAX	chr11:64067965-64068670	HepG2	liver:	n/a	n/a
46	CHD2	chr11:64068106-64068734	H1-hESC	embryonic stem cell:	n/a	n/a
47	MYC	chr11:64068031-64068823	K562	blood:	n/a	n/a
48	MAX	chr11:64068041-64068497	K562	blood:	n/a	n/a
49	CTCF	chr11:64068240-64068390	WI-38	lung:	n/a	n/a
50	MAX	chr11:64067854-64068940	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:64068201..64068706-chr11:64417059..64417670,2	K562	blood:
2	chr11:64067348..64069448-chr11:64121257..64124209,2	K562	blood:
3	chr11:64033188..64045448-chr11:64059274..64075790,38	MCF-7	breast:
4	chr11:63992244..63993214-chr11:64068161..64068696,2	K562	blood:
5	chr11:64028825..64031822-chr11:64066908..64069442,2	MCF-7	breast:
6	chr11:64066836..64070235-chr11:64070747..64073935,5	MCF-7	breast:
7	chr11:64003628..64022712-chr11:64064086..64078429,56	MCF-7	breast:
8	chr11:63971720..63972767-chr11:64067921..64069107,6	K562	blood:
9	chr11:63962905..63964449-chr11:64068026..64070756,2	MCF-7	breast:
10	chr11:64036497..64040979-chr11:64067017..64069343,5	MCF-7	breast:
11	chr11:64053956..64054808-chr11:64068204..64069163,2	MCF-7	breast:
12	chr11:63932166..63933935-chr11:64068001..64069547,2	MCF-7	breast:
13	chr11:64018424..64019424-chr11:64068141..64069014,5	K562	blood:
14	chr11:64038644..64039412-chr11:64067782..64068670,2	MCF-7	breast:
15	chr11:64005251..64012775-chr11:64065543..64076594,19	MCF-7	breast:

Variant related genes	Relation type
TEX40	TF binding region
ESRRA	TF binding region
ENSG00000168439	Chromatin interaction
ENSG00000219435	Chromatin interaction
ENSG00000149743	Chromatin interaction
ENSG00000133315	Chromatin interaction
ENSG00000149782	Chromatin interaction
ENSG00000256940	Chromatin interaction
ENSG00000257086	Chromatin interaction
ENSG00000173511	Chromatin interaction
ENSG00000173153	Chromatin interaction
ENSG00000173486	Chromatin interaction
ENSG00000173264	Chromatin interaction
ENSG00000168071	Chromatin interaction
ENSG00000002330	Chromatin interaction
ENSG00000173457	Chromatin interaction

Extended variants
information (count: 59 )
Associated
traits (count: 15 )

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs1047206	0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1059440	1.00[ASW][hapmap]
rs11600990	1.00[ASW][hapmap];0.85[CEU][hapmap];1.00[CHB][hapmap];0.90[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.96[TSI][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11602181	1.00[ASW][hapmap]
rs11603212	1.00[ASW][hapmap]
rs11605738	1.00[ASW][hapmap]
rs11606014	0.82[AFR][1000 genomes];0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11607165	1.00[ASW][hapmap]
rs12575642	1.00[ASW][hapmap]
rs12785488	0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12788266	0.82[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12793347	0.81[EUR][1000 genomes]
rs12794145	1.00[ASW][hapmap]
rs12808002	0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2001003	1.00[ASW][hapmap]
rs2070765	1.00[ASW][hapmap]
rs2276014	1.00[CHB][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2282490	1.00[ASW][hapmap]
rs28395875	0.91[AFR][1000 genomes];0.88[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs28395876	0.91[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs34292685	0.85[CEU][hapmap];0.82[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs35692796	0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs41294396	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs477895	0.85[CEU][hapmap];0.85[MEX][hapmap];0.93[TSI][hapmap];0.96[EUR][1000 genomes]
rs66968227	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71456304	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs71456309	0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7938380	0.82[AFR][1000 genomes];0.95[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs7939107	0.82[AFR][1000 genomes];0.95[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs7939784	1.00[ASW][hapmap]
rs7947143	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs882146	1.00[ASW][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:15)

SNP	Gene	Cis/trans	Tissue	Source
rs2286614	CPSF7	cis	cerebellum	SCAN
rs2286614	ASRGL1	cis	parietal	SCAN
rs2286614	CD248	cis	parietal	SCAN
rs2286614	PRDX5	cis	parietal	SCAN
rs2286614	FAM89B	cis	parietal	SCAN
rs2286614	FLRT1	cis	cerebellum	SCAN
rs2286614	CHKA	cis	cerebellum	SCAN
rs2286614	PPP1R14B	cis	multi-tissue	Pritchard
rs2286614	MALAT1	cis	cerebellum	SCAN
rs2286614	ESRRA	cis	parietal	SCAN
rs2286614	FAU	cis	parietal	SCAN
rs2286614	TRPT1	cis	Muscle Skeletal	GTEx
rs2286614	TEX40	cis	Thyroid	GTEx
rs2286614	CDK2AP2	cis	parietal	SCAN
rs2286614	PPP1R14B	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:64066600-64068400	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr11:64066600-64068400	Bivalent Enhancer	Fetal Brain Male	brain
3	chr11:64066600-64068400	Enhancers	Lung	lung
4	chr11:64066600-64068400	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
5	chr11:64066600-64068600	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr11:64066600-64068600	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr11:64066600-64068600	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr11:64066600-64068600	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr11:64066600-64068600	Flanking Active TSS	Right Ventricle	heart
10	chr11:64066600-64068800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
11	chr11:64066600-64068800	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
12	chr11:64066600-64068800	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
13	chr11:64066800-64068400	Flanking Bivalent TSS/Enh	Adipose Nuclei	Adipose
14	chr11:64066800-64068600	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
15	chr11:64066800-64068600	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
16	chr11:64066800-64068600	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr11:64066800-64068600	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr11:64066800-64068600	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr11:64066800-64068600	Flanking Bivalent TSS/Enh	Colonic Mucosa	Colon
20	chr11:64066800-64068600	Bivalent Enhancer	Fetal Lung	lung
21	chr11:64066800-64068600	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
22	chr11:64066800-64068800	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
23	chr11:64066800-64068800	Flanking Bivalent TSS/Enh	Primary T regulatory cells fromperipheralblood	blood
24	chr11:64066800-64068800	Enhancers	Spleen	Spleen
25	chr11:64067000-64068400	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
26	chr11:64067000-64068400	Enhancers	Gastric	stomach
27	chr11:64067000-64068600	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
28	chr11:64067000-64068800	Flanking Bivalent TSS/Enh	Primary T cells from cord blood	blood
29	chr11:64067000-64068800	Flanking Bivalent TSS/Enh	Primary T helper naive cells fromperipheralblood	blood
30	chr11:64067000-64069000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
31	chr11:64067200-64068400	Flanking Bivalent TSS/Enh	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr11:64067200-64068400	Bivalent Enhancer	Fetal Brain Female	brain
33	chr11:64067200-64068600	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
34	chr11:64067200-64068600	Flanking Active TSS	Brain Substantia Nigra	brain
35	chr11:64067200-64068600	Flanking Bivalent TSS/Enh	HepG2	liver
36	chr11:64067200-64068800	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
37	chr11:64067200-64068800	Flanking Active TSS	Brain Hippocampus Middle	brain
38	chr11:64067200-64068800	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
39	chr11:64067200-64069200	Bivalent Enhancer	Fetal Thymus	thymus
40	chr11:64067200-64069400	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
41	chr11:64067400-64068400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
42	chr11:64067400-64068400	Enhancers	Ovary	ovary
43	chr11:64067400-64068400	Bivalent Enhancer	Placenta Amnion	Placenta Amnion
44	chr11:64067400-64068600	Flanking Active TSS	Brain Anterior Caudate	brain
45	chr11:64067400-64068600	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
46	chr11:64067400-64069000	Flanking Bivalent TSS/Enh	Primary T helper cells PMA-I stimulated	--
47	chr11:64067600-64068400	Flanking Bivalent TSS/Enh	Breast Myoepithelial Primary Cells	Breast
48	chr11:64067600-64068400	Enhancers	Fetal Heart	heart
49	chr11:64067600-64068600	Flanking Bivalent TSS/Enh	Primary neutrophils fromperipheralblood	blood
50	chr11:64067600-64068600	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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