Variant report

Variant	rs2286612
Chromosome Location	chr11:63994230-63994231
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	FOXM1	chr11:63993010-63994348	GM12878	blood:	n/a	n/a
2	ELF1	chr11:63994104-63994630	K562	blood:	n/a	n/a
3	POLR2A	chr11:63993063-63994621	GM10847	blood:	n/a	n/a
4	ELF1	chr11:63993119-63994612	K562	blood:	n/a	chr11:63993633-63993642 chr11:63993724-63993733
5	HMGN3	chr11:63993156-63994587	K562	blood:	n/a	n/a
6	POLR2A	chr11:63992736-63995293	Hela-S3	cervix:	n/a	n/a
7	POLR2A	chr11:63989232-63995299	K562	blood:	n/a	n/a
8	EBF1	chr11:63993736-63994470	GM12878	blood:	n/a	n/a
9	HCFC1	chr11:63992684-63994367	Hela-S3	cervix:	n/a	n/a
10	YY1	chr11:63993355-63994451	K562	blood:	n/a	chr11:63993647-63993656 chr11:63993645-63993656 chr11:63993947-63993966
11	SIN3AK20	chr11:63994049-63994456	HepG2	liver:	n/a	n/a
12	POLR2A	chr11:63989880-63995323	GM12891	blood:	n/a	n/a
13	POLR2A	chr11:63991338-63994677	GM12891	blood:	n/a	n/a
14	CTCF	chr11:63993207-63994348	K562	blood:	n/a	chr11:63993772-63993790 chr11:63993338-63993356 chr11:63993774-63993787 chr11:63993781-63993794
15	MAZ	chr11:63994087-63994308	HepG2	liver:	n/a	n/a
16	POLR2A	chr11:63991343-63995010	U87	brain:	n/a	n/a
17	MTA3	chr11:63991287-63995175	GM12878	blood:	n/a	n/a
18	SIN3AK20	chr11:63994083-63994537	PANC-1	pancreas:	n/a	n/a
19	POLR2A	chr11:63991349-63994680	GM12891	blood:	n/a	n/a
20	CTCF	chr11:63994200-63994350	SK-N-SH_RA	brain:	n/a	n/a
21	POLR2A	chr11:63991516-63995277	Raji	blood:	n/a	n/a
22	POLR2A	chr11:63991337-63995010	U87	brain:	n/a	n/a
23	NR2F2	chr11:63993181-63994570	K562	blood:	n/a	n/a
24	POLR2A	chr11:63991399-63994678	GM12878	blood:	n/a	n/a
25	POLR2A	chr11:63990418-63994603	GM12878	blood:	n/a	n/a
26	MAX	chr11:63993278-63994277	ECC-1	luminal epithelium:	n/a	n/a
27	POLR2A	chr11:63989946-63994682	HL-60	blood:	n/a	n/a
28	MAX	chr11:63992564-63994729	HepG2	liver:	n/a	chr11:63993229-63993239 chr11:63993079-63993088
29	PAX5	chr11:63993927-63994683	GM12878	blood:	n/a	n/a
30	GABPA	chr11:63993192-63994679	SK-N-SH	brain:	n/a	chr11:63993726-63993733 chr11:63993816-63993825
31	ELK1	chr11:63994179-63994543	K562	blood:	n/a	n/a
32	MAZ	chr11:63992605-63994798	IMR90	lung:	n/a	chr11:63993229-63993239 chr11:63993079-63993088
33	CTCF	chr11:63994160-63994310	GM06990	blood:	n/a	n/a
34	POLR2A	chr11:63990068-63995245	GM18505	blood:	n/a	n/a
35	YY1	chr11:63993391-63994461	HepG2	liver:	n/a	chr11:63993647-63993656 chr11:63993645-63993656 chr11:63993947-63993966
36	TCF7L2	chr11:63993455-63994465	HCT-116	colon:	n/a	n/a
37	POLR2A	chr11:63989981-63995376	GM12892	blood:	n/a	n/a
38	MAX	chr11:63992728-63994709	K562	blood:	n/a	chr11:63993229-63993239 chr11:63993079-63993088
39	GABPA	chr11:63994193-63994455	HepG2	liver:	n/a	n/a
40	POLR2A	chr11:63991347-63994715	GM12892	blood:	n/a	n/a
41	POLR2A	chr11:63993360-63994538	A549	lung:	n/a	n/a
42	CBX3	chr11:63993907-63994396	K562	blood:	n/a	n/a
43	POLR2A	chr11:63993380-63994377	Gliobla	brain:	n/a	n/a
44	ELF1	chr11:63994172-63994521	HepG2	liver:	n/a	n/a
45	GABPA	chr11:63993097-63994506	MCF-7	breast:	n/a	chr11:63993726-63993733 chr11:63993816-63993825
46	MYC	chr11:63993231-63994545	NB4	blood:	n/a	n/a
47	RCOR1	chr11:63993334-63994408	K562	blood:	n/a	n/a
48	ZBTB7A	chr11:63993031-63994618	K562	blood:	n/a	chr11:63993773-63993782 chr11:63993739-63993746
49	EBF1	chr11:63994095-63994514	GM12878	blood:	n/a	n/a
50	POLR2A	chr11:63993283-63994453	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:63932568..63935141-chr11:63993755..63995910,2	MCF-7	breast:
2	chr11:63993205..63994873-chr11:64060700..64063524,2	MCF-7	breast:
3	chr11:63990938..63995618-chr11:64068467..64075569,11	MCF-7	breast:
4	chr11:63993921..63994825-chr9:33001104..33001661,2	Hela-S3	cervix:
5	chr11:63993461..63994315-chr12:13044108..13044821,2	Hela-S3	cervix:
6	chr11:63993605..63994359-chr17:79885128..79885645,2	Hela-S3	cervix:
7	chr11:63579430..63582335-chr11:63993670..63995611,2	K562	blood:
8	chr11:63993441..63994299-chr16:31084853..31085645,2	Hela-S3	cervix:
9	chr11:63962580..63965391-chr11:63991959..63994483,2	MCF-7	breast:
10	chr11:63992108..63994970-chr11:64050201..64053443,5	MCF-7	breast:
11	chr11:63994007..63994575-chr15:60689413..60690315,2	Hela-S3	cervix:
12	chr11:63951654..63956341-chr11:63991514..63996131,9	MCF-7	breast:

Variant related genes	Relation type
DNAJC4	TF binding region
TRPT1	TF binding region
NUDT22	TF binding region
ENSG00000197063	Chromatin interaction
ENSG00000207024	Chromatin interaction
ENSG00000167394	Chromatin interaction
ENSG00000168005	Chromatin interaction
ENSG00000002330	Chromatin interaction
ENSG00000137074	Chromatin interaction
ENSG00000133315	Chromatin interaction
ENSG00000173153	Chromatin interaction
ENSG00000013588	Chromatin interaction
ENSG00000173264	Chromatin interaction
ENSG00000182718	Chromatin interaction
ENSG00000168439	Chromatin interaction
ENSG00000219435	Chromatin interaction

Extended variants
information (count: 79 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs10128649	0.88[ASN][1000 genomes]
rs10556	0.90[ASN][1000 genomes]
rs10897477	0.94[AFR][1000 genomes]
rs11231700	1.00[CEU][hapmap]
rs11231706	1.00[CEU][hapmap]
rs1124660	0.88[CHD][hapmap];0.92[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.91[AMR][1000 genomes]
rs1207462	1.00[CHB][hapmap]
rs1213140	0.84[ASN][1000 genomes]
rs12281471	0.84[ASN][1000 genomes]
rs12283639	0.84[ASN][1000 genomes]
rs12283842	0.87[AFR][1000 genomes]
rs12287065	0.90[ASN][1000 genomes]
rs12574188	1.00[CHB][hapmap]
rs12575515	1.00[CHB][hapmap]
rs12575690	0.82[ASN][1000 genomes]
rs1468558	1.00[CHB][hapmap];0.82[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.90[ASN][1000 genomes]
rs17158870	1.00[CEU][hapmap];0.81[YRI][hapmap]
rs17159027	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs1783518	0.89[CHB][hapmap]
rs2079786	1.00[MEX][hapmap]
rs2232410	1.00[CHB][hapmap];0.82[JPT][hapmap];1.00[MEX][hapmap];0.88[ASN][1000 genomes]
rs2282548	1.00[CHB][hapmap];0.84[ASN][1000 genomes]
rs2289572	0.82[ASN][1000 genomes]
rs2302262	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs3751120	0.81[GIH][hapmap]
rs3759056	0.84[ASN][1000 genomes]
rs41294376	0.82[ASN][1000 genomes]
rs493052	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.86[ASN][1000 genomes]
rs58009222	0.83[ASN][1000 genomes]
rs58694215	0.83[ASN][1000 genomes]
rs58721876	1.00[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs58747362	0.86[ASN][1000 genomes]
rs59283629	0.90[ASN][1000 genomes]
rs59747132	0.83[ASN][1000 genomes]
rs60095771	0.83[ASN][1000 genomes]
rs60421451	0.88[ASN][1000 genomes]
rs60571265	0.81[ASN][1000 genomes]
rs61143549	0.83[ASN][1000 genomes]
rs61431997	0.90[ASN][1000 genomes]
rs61629200	0.92[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs621816	0.90[ASN][1000 genomes]
rs7102415	0.94[ASW][hapmap];1.00[CEU][hapmap];0.89[GIH][hapmap];0.95[LWK][hapmap];1.00[MEX][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes]
rs7110262	0.90[ASN][1000 genomes]
rs7123004	0.91[AFR][1000 genomes]
rs7934801	0.94[ASW][hapmap];1.00[CEU][hapmap];0.89[GIH][hapmap];0.91[LWK][hapmap];1.00[MEX][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes]
rs7950596	0.94[ASW][hapmap];1.00[CEU][hapmap];0.88[CHD][hapmap];0.89[GIH][hapmap];1.00[JPT][hapmap];0.95[LWK][hapmap];1.00[MEX][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs7950922	0.84[ASN][1000 genomes]
rs7951858	0.88[ASN][1000 genomes]
rs7952435	1.00[JPT][hapmap];1.00[MEX][hapmap]

Variant overlapped rSNPs/rCNVs (count:30 , 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	nsv468592	chr11:63924446-64042997	Enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	166 gene(s)	inside rSNPs	diseases
11	nsv555184	chr11:63924446-64042997	Genic enhancers Enhancers Flanking Active TSS Active TSS Strong transcription Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	166 gene(s)	inside rSNPs	diseases
12	nsv897665	chr11:63927695-64026144	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	155 gene(s)	inside rSNPs	diseases
13	nsv897666	chr11:63929493-64026144	Enhancers Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	155 gene(s)	inside rSNPs	diseases
14	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
15	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
16	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
17	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
18	nsv468595	chr11:63953121-64027888	Enhancers Flanking Active TSS Active TSS Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	146 gene(s)	inside rSNPs	diseases
19	nsv555187	chr11:63953121-64027888	Strong transcription Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	146 gene(s)	inside rSNPs	diseases
20	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
21	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
22	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
23	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
24	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
25	nsv541061	chr11:63970174-64010995	Strong transcription Active TSS Flanking Active TSS Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	76 gene(s)	inside rSNPs	diseases
26	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
27	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
28	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
29	nsv897673	chr11:63991581-64018687	Flanking Active TSS Bivalent/Poised TSS Genic enhancers Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	92 gene(s)	inside rSNPs	diseases
30	esv992196	chr11:63992534-64002355	Active TSS Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:63992400-63995200	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
2	chr11:63992600-63994400	Active TSS	Thymus	Thymus
3	chr11:63992600-63995200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr11:63992600-63995200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr11:63992600-63995400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
6	chr11:63992800-63994400	Active TSS	HUES48 Cell Line	embryonic stem cell
7	chr11:63992800-63994800	Transcr. at gene 5' and 3'	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr11:63992800-63995000	Active TSS	H9 Cell Line	embryonic stem cell
9	chr11:63992800-63995000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr11:63992800-63995000	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
11	chr11:63992800-63995200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
12	chr11:63992800-63995200	Flanking Active TSS	Adipose Nuclei	Adipose
13	chr11:63993000-63994400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
14	chr11:63993000-63994400	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr11:63993000-63994400	Active TSS	Psoas Muscle	Psoas
16	chr11:63993000-63994400	Active TSS	NHLF	lung
17	chr11:63993000-63994600	Active TSS	ES-I3 Cell Line	embryonic stem cell
18	chr11:63993000-63994600	Active TSS	iPS-18 Cell Line	embryonic stem cell
19	chr11:63993000-63994800	Flanking Active TSS	Primary hematopoietic stem cells	blood
20	chr11:63993000-63994800	Active TSS	Aorta	Aorta
21	chr11:63993000-63995000	Flanking Active TSS	Primary B cells from cord blood	blood
22	chr11:63993000-63995000	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
23	chr11:63993000-63995000	Active TSS	HSMMtube	muscle
24	chr11:63993000-63995200	Active TSS	Fetal Kidney	kidney
25	chr11:63993000-63995200	Active TSS	Pancreatic Islets	Pancreatic Islet
26	chr11:63993000-63995400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr11:63993200-63994400	Active TSS	iPS-20b Cell Line	embryonic stem cell
28	chr11:63993200-63994400	Active TSS	Duodenum Smooth Muscle	Duodenum
29	chr11:63993200-63994400	Active TSS	Esophagus	oesophagus
30	chr11:63993200-63994400	Active TSS	Left Ventricle	heart
31	chr11:63993200-63994400	Active TSS	Pancreas	Pancrea
32	chr11:63993200-63994400	Active TSS	Sigmoid Colon	Sigmoid Colon
33	chr11:63993200-63994400	Active TSS	Stomach Mucosa	stomach
34	chr11:63993200-63994400	Bivalent/Poised TSS	HepG2	liver
35	chr11:63993200-63994400	Active TSS	HSMM	muscle
36	chr11:63993200-63994400	Active TSS	K562	blood
37	chr11:63993200-63994600	Active TSS	Small Intestine	intestine
38	chr11:63993200-63994600	Active TSS	GM12878-XiMat	blood
39	chr11:63993200-63995200	Active TSS	iPS-15b Cell Line	embryonic stem cell
40	chr11:63993200-63995400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
41	chr11:63993400-63994400	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
42	chr11:63993400-63994400	Active TSS	Primary T helper naive cells from peripheral blood	blood
43	chr11:63993400-63994400	Active TSS	Primary T helper cells PMA-I stimulated	--
44	chr11:63993400-63994400	Active TSS	Brain Inferior Temporal Lobe	brain
45	chr11:63993400-63994400	Active TSS	Gastric	stomach
46	chr11:63993600-63994400	Active TSS	Primary T killer memory cells from peripheral blood	blood
47	chr11:63993600-63995400	Enhancers	Fetal Heart	heart
48	chr11:63993800-63994400	Active TSS	Right Atrium	heart
49	chr11:63993800-63994600	Flanking Active TSS	HUVEC	blood vessel
50	chr11:63993800-63994800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived

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