Variant report

Variant	rs139864558
Chromosome Location	chr11:3663224-3663225
allele	-/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	EGR1	chr11:3663120-3663955	H1-hESC	embryonic stem cell:	n/a	chr11:3663230-3663252 chr11:3663235-3663246 chr11:3663234-3663247 chr11:3663122-3663135 chr11:3663263-3663273 chr11:3663234-3663247 chr11:3663234-3663247 chr11:3663237-3663246 chr11:3663264-3663277 chr11:3663239-3663249 chr11:3663386-3663399 chr11:3663284-3663297 chr11:3663236-3663246 chr11:3663234-3663247 chr11:3663234-3663248 chr11:3663235-3663246 chr11:3663236-3663246 chr11:3663233-3663248
2	ETS1	chr11:3663146-3663758	K562	blood:	n/a	chr11:3663266-3663277 chr11:3663389-3663400 chr11:3663264-3663275
3	SP1	chr11:3663201-3664211	H1-hESC	embryonic stem cell:	n/a	chr11:3663238-3663250 chr11:3663239-3663249 chr11:3663263-3663272 chr11:3663283-3663292 chr11:3663964-3663973 chr11:3663962-3663974 chr11:3663269-3663278 chr11:3663271-3663284 chr11:3663240-3663249 chr11:3663238-3663250 chr11:3663963-3663972 chr11:3663668-3663679 chr11:3663298-3663308 chr11:3663239-3663249 chr11:3664181-3664195 chr11:3663391-3663400 chr11:3663963-3663977 chr11:3663270-3663279 chr11:3663233-3663243 chr11:3663281-3663293 chr11:3663962-3663974 chr11:3663239-3663248 chr11:3663963-3663973
4	ZBTB7A	chr11:3663005-3664016	K562	blood:	n/a	n/a
5	TAF1	chr11:3662962-3663246	H1-hESC	embryonic stem cell:	n/a	n/a
6	TAF1	chr11:3663200-3663720	ECC-1	luminal epithelium:	n/a	n/a
7	MAX	chr11:3663197-3664228	HepG2	liver:	n/a	chr11:3663836-3663849 chr11:3663836-3663851 chr11:3663838-3663848 chr11:3663834-3663849 chr11:3663838-3663847 chr11:3663839-3663846 chr11:3663836-3663849 chr11:3663239-3663249 chr11:3663836-3663849 chr11:3663838-3663847 chr11:3663837-3663848 chr11:3663837-3663848 chr11:3663236-3663245 chr11:3663837-3663847
8	NR2F2	chr11:3663109-3664757	K562	blood:	n/a	chr11:3664088-3664103
9	POLR2A	chr11:3662943-3663728	PANC-1	pancreas:	n/a	n/a
10	ATF2	chr11:3663209-3663719	H1-hESC	embryonic stem cell:	n/a	n/a
11	POLR2A	chr11:3662912-3663706	ECC-1	luminal epithelium:	n/a	n/a
12	MAX	chr11:3662983-3664206	HepG2	liver:	n/a	chr11:3663836-3663849 chr11:3663836-3663851 chr11:3663838-3663848 chr11:3663834-3663849 chr11:3663838-3663847 chr11:3663839-3663846 chr11:3663836-3663849 chr11:3663239-3663249 chr11:3663836-3663849 chr11:3663838-3663847 chr11:3663837-3663848 chr11:3663837-3663848 chr11:3663236-3663245 chr11:3663837-3663847
13	RCOR1	chr11:3663172-3664281	K562	blood:	n/a	n/a
14	E2F4	chr11:3663185-3664014	K562	blood:	n/a	chr11:3663263-3663272 chr11:3663243-3663253
15	IRF1	chr11:3663099-3663626	K562	blood:	n/a	chr11:3663279-3663293 chr11:3663238-3663252 chr11:3663126-3663140
16	POLR2A	chr11:3663000-3664101	HepG2	liver:	n/a	n/a
17	POLR2A	chr11:3663186-3663957	HepG2	liver:	n/a	n/a
18	CCNT2	chr11:3663210-3664109	K562	blood:	n/a	chr11:3663964-3663973
19	MAX	chr11:3663212-3664218	H1-hESC	embryonic stem cell:	n/a	chr11:3663836-3663849 chr11:3663836-3663851 chr11:3663838-3663848 chr11:3663834-3663849 chr11:3663838-3663847 chr11:3663839-3663846 chr11:3663836-3663849 chr11:3663239-3663249 chr11:3663836-3663849 chr11:3663838-3663847 chr11:3663837-3663848 chr11:3663837-3663848 chr11:3663236-3663245 chr11:3663837-3663847
20	POLR2A	chr11:3662972-3664221	H1-hESC	embryonic stem cell:	n/a	n/a
21	POLR2A	chr11:3663176-3663704	K562	blood:	n/a	n/a
22	TAF7	chr11:3663030-3664063	H1-hESC	embryonic stem cell:	n/a	n/a
23	MAZ	chr11:3663205-3664294	K562	blood:	n/a	chr11:3663836-3663849 chr11:3663836-3663851 chr11:3663838-3663848 chr11:3663834-3663849 chr11:3663838-3663847 chr11:3663839-3663846 chr11:3663836-3663849 chr11:3663239-3663249 chr11:3663836-3663849 chr11:3663838-3663847 chr11:3663837-3663848 chr11:3663837-3663848 chr11:3663236-3663245 chr11:3663837-3663847
24	POLR2A	chr11:3663061-3664252	K562	blood:	n/a	n/a
25	SIN3A	chr11:3663053-3664353	H1-hESC	embryonic stem cell:	n/a	chr11:3663455-3663464
26	POLR2A	chr11:3662992-3663965	HEK293	kidney:	n/a	n/a
27	HMGN3	chr11:3663094-3664052	K562	blood:	n/a	n/a
28	POLR2A	chr11:3662921-3663745	HepG2	liver:	n/a	n/a
29	ELF1	chr11:3663140-3663640	K562	blood:	n/a	chr11:3663568-3663580
30	TAF1	chr11:3663180-3663712	K562	blood:	n/a	n/a
31	POLR2A	chr11:3662821-3664519	H1-hESC	embryonic stem cell:	n/a	n/a
32	POLR2A	chr11:3663168-3663689	K562	blood:	n/a	n/a
33	HEY1	chr11:3662954-3663734	HepG2	liver:	n/a	chr11:3663263-3663278 chr11:3663386-3663401 chr11:3663234-3663249 chr11:3663559-3663574 chr11:3663461-3663476
34	HEY1	chr11:3662915-3663266	K562	blood:	n/a	chr11:3663234-3663249
35	ZBTB7A	chr11:3663219-3664129	ECC-1	luminal epithelium:	n/a	n/a
36	MAZ	chr11:3662941-3664236	IMR90	lung:	n/a	chr11:3663836-3663849 chr11:3663836-3663851 chr11:3663838-3663848 chr11:3663834-3663849 chr11:3663838-3663847 chr11:3663839-3663846 chr11:3663836-3663849 chr11:3663239-3663249 chr11:3663836-3663849 chr11:3663838-3663847 chr11:3663837-3663848 chr11:3663837-3663848 chr11:3663236-3663245 chr11:3663837-3663847
37	CEBPD	chr11:3663218-3663659	HepG2	liver:	n/a	n/a
38	E2F6	chr11:3663024-3664064	H1-hESC	embryonic stem cell:	n/a	chr11:3663263-3663272 chr11:3663243-3663253
39	EGR1	chr11:3663076-3663639	K562	blood:	n/a	chr11:3663230-3663252 chr11:3663235-3663246 chr11:3663234-3663247 chr11:3663122-3663135 chr11:3663263-3663273 chr11:3663234-3663247 chr11:3663234-3663247 chr11:3663237-3663246 chr11:3663264-3663277 chr11:3663239-3663249 chr11:3663386-3663399 chr11:3663284-3663297 chr11:3663236-3663246 chr11:3663234-3663247 chr11:3663234-3663248 chr11:3663235-3663246 chr11:3663236-3663246 chr11:3663233-3663248
40	EGR1	chr11:3662961-3664090	HCT-116	colon:	n/a	chr11:3663230-3663252 chr11:3663235-3663246 chr11:3663234-3663247 chr11:3662973-3662982 chr11:3663122-3663135 chr11:3663263-3663273 chr11:3663234-3663247 chr11:3663234-3663247 chr11:3663237-3663246 chr11:3663264-3663277 chr11:3663239-3663249 chr11:3663386-3663399 chr11:3663284-3663297 chr11:3663236-3663246 chr11:3663234-3663247 chr11:3663234-3663248 chr11:3663235-3663246 chr11:3663236-3663246 chr11:3663233-3663248
41	RAD21	chr11:3663216-3663711	H1-hESC	embryonic stem cell:	n/a	chr11:3663424-3663438 chr11:3663423-3663437 chr11:3663573-3663587
42	TBP	chr11:3662870-3664168	H1-hESC	embryonic stem cell:	n/a	n/a
43	MAX	chr11:3663196-3664246	K562	blood:	n/a	chr11:3663836-3663849 chr11:3663836-3663851 chr11:3663838-3663848 chr11:3663834-3663849 chr11:3663838-3663847 chr11:3663839-3663846 chr11:3663836-3663849 chr11:3663239-3663249 chr11:3663836-3663849 chr11:3663838-3663847 chr11:3663837-3663848 chr11:3663837-3663848 chr11:3663236-3663245 chr11:3663837-3663847
44	POLR2A	chr11:3663058-3663235	H1-hESC	embryonic stem cell:	n/a	n/a
45	POLR2A	chr11:3662881-3664045	K562	blood:	n/a	n/a
46	ELF1	chr11:3663163-3663597	K562	blood:	n/a	chr11:3663568-3663580
47	EGR1	chr11:3663089-3663972	K562	blood:	n/a	chr11:3663230-3663252 chr11:3663235-3663246 chr11:3663234-3663247 chr11:3663122-3663135 chr11:3663263-3663273 chr11:3663234-3663247 chr11:3663234-3663247 chr11:3663237-3663246 chr11:3663264-3663277 chr11:3663239-3663249 chr11:3663386-3663399 chr11:3663284-3663297 chr11:3663236-3663246 chr11:3663234-3663247 chr11:3663234-3663248 chr11:3663235-3663246 chr11:3663236-3663246 chr11:3663233-3663248
48	MAX	chr11:3663219-3664222	A549	lung:	n/a	chr11:3663836-3663849 chr11:3663836-3663851 chr11:3663838-3663848 chr11:3663834-3663849 chr11:3663838-3663847 chr11:3663839-3663846 chr11:3663836-3663849 chr11:3663239-3663249 chr11:3663836-3663849 chr11:3663838-3663847 chr11:3663837-3663848 chr11:3663837-3663848 chr11:3663236-3663245 chr11:3663837-3663847
49	JUN	chr11:3662400-3664604	K562	blood:	n/a	chr11:3663264-3663273 chr11:3663659-3663670
50	POLR2A	chr11:3662930-3664732	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:3663198-3663248	HCT-116	colon:	n/a
2	chr11:3663198-3663248	HCM	heart:	n/a
3	chr11:3663198-3663248	NH-A	brain:	n/a
4	chr11:3663198-3663248	AG04449	skin:	fetal
5	chr11:3663198-3663248	GM12891	blood:	n/a
6	chr11:3663198-3663248	GM12892	blood:	n/a
7	chr11:3663198-3663248	SKMC	muscle:	n/a
8	chr11:3663198-3663248	HL-60	blood:	n/a
9	chr11:3663198-3663248	IMR90	lung:	fetal
10	chr11:3663198-3663248	HAEpiC	amniotic membrane:	n/a
11	chr11:3663198-3663248	NHBE	bronchial:	n/a
12	chr11:3663198-3663248	A549	lung:	n/a
13	chr11:3663198-3663248	NHDF-neo	bronchial:	n/a
14	chr11:3663198-3663248	MCF10A-Er-Src	breast:	n/a
15	chr11:3663198-3663248	NT2-D1	testis:	n/a
16	chr11:3663198-3663248	Jurkat	blood:	n/a
17	chr11:3663198-3663248	HEK293	kidney:	embryo
18	chr11:3663198-3663248	HEEpiC	esophagus:	n/a
19	chr11:3663198-3663248	Hepatocyte	liver:	n/a
20	chr11:3663198-3663248	SAEC	small airway:	n/a
21	chr11:3663198-3663248	HCPEpiC	choroid plexus:	n/a
22	chr11:3663198-3663248	ECC-1	luminal epithelium:	n/a
23	chr11:3663198-3663248	PrEC	prostate:	n/a
24	chr11:3663198-3663248	SK-N-MC	brain:	n/a
25	chr11:3663198-3663248	Caco-2	colon:	n/a
26	chr11:3663198-3663248	HepG2	liver:	n/a
27	chr11:3663198-3663248	SK-N-SH	brain:	n/a
28	chr11:3663198-3663248	HRCEpiC	kidney:	n/a
29	chr11:3663198-3663248	ovcar-3	ovarian:	n/a
30	chr11:3663198-3663248	GM19239	blood:	n/a
31	chr11:3663198-3663248	SK-N-SH_RA	brain:	n/a
32	chr11:3663198-3663248	MCF-7	breast:	n/a
33	chr11:3663198-3663248	Hela-S3	cervix:	n/a
34	chr11:3663198-3663248	HMEC	breast:	n/a
35	chr11:3663198-3663248	LNCaP	prostate:	n/a
36	chr11:3663198-3663248	RPTEC	kidney:	n/a
37	chr11:3663198-3663248	PFSK-1	brain:	n/a
38	chr11:3663198-3663248	AG09319	gingival:	n/a
39	chr11:3663198-3663248	AG09309	skin:	n/a
40	chr11:3663198-3663248	HPAEpiC	pulmonary alveolar:	n/a
41	chr11:3663198-3663248	U87	brain:	n/a
42	chr11:3663198-3663248	CMK	blood:	n/a
43	chr11:3663198-3663248	HRPEpiC	eye:	n/a
44	chr11:3663198-3663248	NB4	blood:	n/a
45	chr11:3663198-3663248	AG04450	lung:	fetal
46	chr11:3663198-3663248	HRE	kidney:	n/a
47	chr11:3663198-3663248	BE2_C	brain:	n/a
48	chr11:3663198-3663248	HCF	heart:	n/a
49	chr11:3663198-3663248	HUVEC	blood vessel:	n/a
50	chr11:3663198-3663248	AoSMC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:3663179..3665930-chr11:3817516..3820122,2	K562	blood:
2	chr11:3661894..3664122-chr11:3664715..3667131,2	K562	blood:

Variant related genes	Relation type
ART1	TF binding region
ART5	TF binding region
ART1	CpG island
ART5	CpG island
ENSG00000148985	Chromatin interaction
ENSG00000110713	Chromatin interaction
ENSG00000129744	Chromatin interaction

Extended variants
information (count: 18 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1047763	chr11:2918998-3751029	Strong transcription Bivalent Enhancer Flanking Active TSS Enhancers Genic enhancers Weak transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
2	esv2758252	chr11:3236512-3801429	Weak transcription Enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
3	esv2759796	chr11:3236512-3801429	Strong transcription Enhancers ZNF genes & repeats Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
4	esv2760300	chr11:3416489-3667988	Flanking Active TSS Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
5	esv18699	chr11:3426081-3674989	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Weak transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
6	nsv832051	chr11:3523947-3728714	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
7	esv1820972	chr11:3616884-3801429	Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
8	esv1821329	chr11:3616884-3801429	Strong transcription Weak transcription Enhancers Genic enhancers Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
9	nsv832052	chr11:3616884-3801429	Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
10	nsv428247	chr11:3616884-3801429	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Enhancers Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
11	nsv526441	chr11:3626177-3756686	Strong transcription Weak transcription ZNF genes & repeats Enhancers Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
12	nsv1046356	chr11:3628837-3774215	Genic enhancers Strong transcription Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
13	nsv1044345	chr11:3628912-3739222	Enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
14	nsv540906	chr11:3628912-3739222	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
15	nsv1044419	chr11:3628912-3751029	Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription Genic enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
16	nsv1052573	chr11:3637802-3665561	Weak transcription Bivalent/Poised TSS Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
17	esv2760179	chr11:3652893-3677096	Bivalent Enhancer Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
18	nsv8775	chr11:3663012-3664867	Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:97 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:3662400-3663400	Weak transcription	Right Atrium	heart
2	chr11:3662400-3663800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr11:3662600-3663800	Active TSS	Skeletal Muscle Female	skeletal muscle
4	chr11:3662600-3664600	Active TSS	H9 Cell Line	embryonic stem cell
5	chr11:3662800-3663400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
6	chr11:3662800-3663400	Active TSS	Stomach Smooth Muscle	stomach
7	chr11:3662800-3663600	Bivalent/Poised TSS	Brain Germinal Matrix	brain
8	chr11:3662800-3663800	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
9	chr11:3662800-3663800	Enhancers	Fetal Brain Male	brain
10	chr11:3662800-3663800	Active TSS	Rectal Smooth Muscle	rectum
11	chr11:3662800-3664000	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr11:3662800-3664200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr11:3662800-3664200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr11:3662800-3664200	Active TSS	HUES48 Cell Line	embryonic stem cell
15	chr11:3662800-3664400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
16	chr11:3662800-3664400	Active TSS	Fetal Kidney	kidney
17	chr11:3662800-3664600	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr11:3662800-3664600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr11:3662800-3664800	Active TSS	HUES64 Cell Line	embryonic stem cell
20	chr11:3662800-3664800	Active TSS	iPS-15b Cell Line	embryonic stem cell
21	chr11:3663000-3663400	Bivalent Enhancer	Primary B cells from peripheral blood	blood
22	chr11:3663000-3663400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
23	chr11:3663000-3663400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
24	chr11:3663000-3663400	Active TSS	Primary T helper cells fromperipheralblood	blood
25	chr11:3663000-3663400	Flanking Bivalent TSS/Enh	Primary T regulatory cells fromperipheralblood	blood
26	chr11:3663000-3663400	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
27	chr11:3663000-3663400	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr11:3663000-3663400	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr11:3663000-3663400	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr11:3663000-3663400	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr11:3663000-3663400	Bivalent/Poised TSS	Primary mononuclear cells fromperipheralblood	Blood
32	chr11:3663000-3663400	Enhancers	Adipose Nuclei	Adipose
33	chr11:3663000-3663400	Active TSS	Colonic Mucosa	Colon
34	chr11:3663000-3663400	Flanking Bivalent TSS/Enh	Duodenum Smooth Muscle	Duodenum
35	chr11:3663000-3663400	Enhancers	Fetal Lung	lung
36	chr11:3663000-3663400	Bivalent Enhancer	Placenta	Placenta
37	chr11:3663000-3663400	Bivalent Enhancer	HMEC	breast
38	chr11:3663000-3663400	Bivalent/Poised TSS	HSMMtube	muscle
39	chr11:3663000-3663400	Active TSS	NH-A	brain
40	chr11:3663000-3663600	Active TSS	Primary T helper naive cells fromperipheralblood	blood
41	chr11:3663000-3663600	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
42	chr11:3663000-3663600	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr11:3663000-3663600	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
44	chr11:3663000-3663600	Active TSS	Pancreas	Pancrea
45	chr11:3663000-3663600	Active TSS	Placenta Amnion	Placenta Amnion
46	chr11:3663000-3663600	Active TSS	Psoas Muscle	Psoas
47	chr11:3663000-3663800	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr11:3663000-3663800	Active TSS	Colon Smooth Muscle	Colon
49	chr11:3663000-3663800	Active TSS	Fetal Brain Female	brain
50	chr11:3663000-3663800	Enhancers	Fetal Heart	heart

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