Variant report

Variant	rs7924355
Chromosome Location	chr11:3663552-3663553
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	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	POLR2A	chr11:3663383-3663617	MCF-7	breast:	n/a	n/a
3	HEY1	chr11:3663304-3663706	K562	blood:	n/a	chr11:3663386-3663401 chr11:3663559-3663574 chr11:3663461-3663476
4	E2F6	chr11:3663287-3664017	K562	blood:	n/a	n/a
5	SP1	chr11:3663315-3663609	H1-hESC	embryonic stem cell:	n/a	chr11:3663391-3663400
6	HDAC2	chr11:3663500-3663710	K562	blood:	n/a	n/a
7	ETS1	chr11:3663146-3663758	K562	blood:	n/a	chr11:3663266-3663277 chr11:3663389-3663400 chr11:3663264-3663275
8	UBTF	chr11:3663339-3663569	K562	blood:	n/a	n/a
9	TCF7L2	chr11:3663360-3663587	Hela-S3	cervix:	n/a	n/a
10	POLR2A	chr11:3663285-3664031	K562	blood:	n/a	n/a
11	TCF12	chr11:3663362-3663568	H1-hESC	embryonic stem cell:	n/a	n/a
12	USF2	chr11:3663430-3664127	H1-hESC	embryonic stem cell:	n/a	chr11:3663567-3663583 chr11:3663836-3663847 chr11:3663448-3663464
13	JUND	chr11:3663355-3664195	H1-hESC	embryonic stem cell:	n/a	chr11:3663659-3663670
14	TAF7	chr11:3663352-3663644	K562	blood:	n/a	n/a
15	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
16	SMC3	chr11:3663525-3663552	K562	blood:	n/a	n/a
17	POLR2A	chr11:3663281-3663668	HCT-116	colon:	n/a	n/a
18	KAP1	chr11:3663456-3664982	HEK293	kidney:	n/a	n/a
19	EP300	chr11:3663263-3663733	H1-hESC	embryonic stem cell:	n/a	n/a
20	ZBTB7A	chr11:3663005-3664016	K562	blood:	n/a	n/a
21	TAF1	chr11:3663200-3663720	ECC-1	luminal epithelium:	n/a	n/a
22	UBTF	chr11:3663250-3664171	K562	blood:	n/a	n/a
23	EP300	chr11:3663306-3663684	HepG2	liver:	n/a	n/a
24	HCFC1	chr11:3663332-3664011	K562	blood:	n/a	n/a
25	SMC3	chr11:3663386-3663574	Hela-S3	cervix:	n/a	n/a
26	MAX	chr11:3663397-3664040	Hela-S3	cervix:	n/a	chr11:3663836-3663849 chr11:3663836-3663851 chr11:3663838-3663848 chr11:3663834-3663849 chr11:3663838-3663847 chr11:3663839-3663846 chr11:3663836-3663849 chr11:3663836-3663849 chr11:3663838-3663847 chr11:3663837-3663848 chr11:3663837-3663848 chr11:3663837-3663847
27	E2F6	chr11:3663278-3664078	K562	blood:	n/a	n/a
28	TAF1	chr11:3663307-3664154	H1-hESC	embryonic stem cell:	n/a	n/a
29	ZBTB7A	chr11:3663434-3663827	HepG2	liver:	n/a	n/a
30	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
31	CTCF	chr11:3663480-3663630	HCPEpiC	choroid plexus:	n/a	chr11:3663574-3663587
32	IRF1	chr11:3663306-3663575	K562	blood:	n/a	n/a
33	POLR2A	chr11:3663288-3663938	MCF-7	breast:	n/a	n/a
34	GTF2F1	chr11:3663372-3664144	H1-hESC	embryonic stem cell:	n/a	n/a
35	NR2F2	chr11:3663109-3664757	K562	blood:	n/a	chr11:3664088-3664103
36	POLR2A	chr11:3662943-3663728	PANC-1	pancreas:	n/a	n/a
37	ATF2	chr11:3663209-3663719	H1-hESC	embryonic stem cell:	n/a	n/a
38	ZNF143	chr11:3663358-3664493	H1-hESC	embryonic stem cell:	n/a	chr11:3663455-3663465 chr11:3664445-3664463 chr11:3663862-3663880 chr11:3664184-3664202
39	MYBL2	chr11:3663267-3663813	HepG2	liver:	n/a	n/a
40	MAX	chr11:3663407-3664068	Hela-S3	cervix:	n/a	chr11:3663836-3663849 chr11:3663836-3663851 chr11:3663838-3663848 chr11:3663834-3663849 chr11:3663838-3663847 chr11:3663839-3663846 chr11:3663836-3663849 chr11:3663836-3663849 chr11:3663838-3663847 chr11:3663837-3663848 chr11:3663837-3663848 chr11:3663837-3663847
41	TAF1	chr11:3663260-3664058	H1-hESC	embryonic stem cell:	n/a	n/a
42	HEY1	chr11:3663260-3664056	HepG2	liver:	n/a	chr11:3663263-3663278 chr11:3663386-3663401 chr11:3663559-3663574 chr11:3663461-3663476
43	TBP	chr11:3663306-3664022	K562	blood:	n/a	n/a
44	MAZ	chr11:3663305-3663583	Hela-S3	cervix:	n/a	n/a
45	POLR2A	chr11:3662912-3663706	ECC-1	luminal epithelium:	n/a	n/a
46	JUN	chr11:3663486-3663874	H1-hESC	embryonic stem cell:	n/a	chr11:3663659-3663670
47	HDAC2	chr11:3663322-3663605	HepG2	liver:	n/a	n/a
48	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
49	MAX	chr11:3663492-3663572	A549	lung:	n/a	n/a
50	RCOR1	chr11:3663172-3664281	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:3663511-3663561	HUVEC	blood vessel:	n/a
2	chr11:3663543-3663593	HRE	kidney:	n/a
3	chr11:3663511-3663561	HRPEpiC	eye:	n/a
4	chr11:3663511-3663561	MCF-7	breast:	n/a
5	chr11:3663543-3663593	A549	lung:	n/a
6	chr11:3663532-3663582	SK-N-MC	brain:	n/a
7	chr11:3663532-3663582	GM12891	blood:	n/a
8	chr11:3663532-3663582	GM12892	blood:	n/a
9	chr11:3663511-3663561	HMEC	breast:	n/a
10	chr11:3663511-3663561	SK-N-SH	brain:	n/a
11	chr11:3663543-3663593	RPTEC	kidney:	n/a
12	chr11:3663511-3663561	LNCaP	prostate:	n/a
13	chr11:3663511-3663561	SKMC	muscle:	n/a
14	chr11:3663543-3663593	GM12891	blood:	n/a
15	chr11:3663511-3663561	AG04449	skin:	fetal
16	chr11:3663543-3663593	HRCEpiC	kidney:	n/a
17	chr11:3663543-3663593	GM19239	blood:	n/a
18	chr11:3663511-3663561	IMR90	lung:	fetal
19	chr11:3663543-3663593	HMEC	breast:	n/a
20	chr11:3663532-3663582	NHBE	bronchial:	n/a
21	chr11:3663532-3663582	HIPEpiC	eye:	n/a
22	chr11:3663543-3663593	AG04450	lung:	fetal
23	chr11:3663532-3663582	GM06990	blood:	n/a
24	chr11:3663511-3663561	ECC-1	luminal epithelium:	n/a
25	chr11:3663511-3663561	HL-60	blood:	n/a
26	chr11:3663511-3663561	SK-N-SH_RA	brain:	n/a
27	chr11:3663511-3663561	AG04450	lung:	fetal
28	chr11:3663543-3663593	LNCaP	prostate:	n/a
29	chr11:3663511-3663561	GM12878	blood:	n/a
30	chr11:3663532-3663582	BE2_C	brain:	n/a
31	chr11:3663511-3663561	RPTEC	kidney:	n/a
32	chr11:3663511-3663561	CMK	blood:	n/a
33	chr11:3663532-3663582	PANC-1	pancreas:	n/a
34	chr11:3663511-3663561	GM19239	blood:	n/a
35	chr11:3663532-3663582	T-47D	breast:	n/a
36	chr11:3663511-3663561	HEEpiC	esophagus:	n/a
37	chr11:3663511-3663561	SK-N-MC	brain:	n/a
38	chr11:3663511-3663561	HCPEpiC	choroid plexus:	n/a
39	chr11:3663543-3663593	H1-hESC	embryonic stem cell:	embryo
40	chr11:3663532-3663582	HUVEC	blood vessel:	n/a
41	chr11:3663532-3663582	PFSK-1	brain:	n/a
42	chr11:3663532-3663582	ovcar-3	ovarian:	n/a
43	chr11:3663532-3663582	AG09319	gingival:	n/a
44	chr11:3663532-3663582	HCF	heart:	n/a
45	chr11:3663511-3663561	T-47D	breast:	n/a
46	chr11:3663532-3663582	RPTEC	kidney:	n/a
47	chr11:3663511-3663561	ovcar-3	ovarian:	n/a
48	chr11:3663543-3663593	HNPCEpiC	eye:	n/a
49	chr11:3663543-3663593	AG09319	gingival:	n/a
50	chr11:3663511-3663561	HIPEpiC	eye:	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
ART5	TF binding region
ART1	TF binding region
ART1	CpG island
ART5	CpG island
ENSG00000129744	Chromatin interaction
ENSG00000148985	Chromatin interaction
ENSG00000110713	Chromatin interaction

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs12295190	1.00[EUR][1000 genomes]
rs16929858	1.00[EUR][1000 genomes]
rs16929943	1.00[EUR][1000 genomes]
rs2231537	1.00[EUR][1000 genomes]
rs74050772	1.00[EUR][1000 genomes]
rs868713	1.00[EUR][1000 genomes]

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:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:3662400-3663800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr11:3662600-3663800	Active TSS	Skeletal Muscle Female	skeletal muscle
3	chr11:3662600-3664600	Active TSS	H9 Cell Line	embryonic stem cell
4	chr11:3662800-3663600	Bivalent/Poised TSS	Brain Germinal Matrix	brain
5	chr11:3662800-3663800	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
6	chr11:3662800-3663800	Enhancers	Fetal Brain Male	brain
7	chr11:3662800-3663800	Active TSS	Rectal Smooth Muscle	rectum
8	chr11:3662800-3664000	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr11:3662800-3664200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr11:3662800-3664200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr11:3662800-3664200	Active TSS	HUES48 Cell Line	embryonic stem cell
12	chr11:3662800-3664400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
13	chr11:3662800-3664400	Active TSS	Fetal Kidney	kidney
14	chr11:3662800-3664600	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr11:3662800-3664600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr11:3662800-3664800	Active TSS	HUES64 Cell Line	embryonic stem cell
17	chr11:3662800-3664800	Active TSS	iPS-15b Cell Line	embryonic stem cell
18	chr11:3663000-3663600	Active TSS	Primary T helper naive cells fromperipheralblood	blood
19	chr11:3663000-3663600	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
20	chr11:3663000-3663600	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr11:3663000-3663600	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
22	chr11:3663000-3663600	Active TSS	Pancreas	Pancrea
23	chr11:3663000-3663600	Active TSS	Placenta Amnion	Placenta Amnion
24	chr11:3663000-3663600	Active TSS	Psoas Muscle	Psoas
25	chr11:3663000-3663800	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr11:3663000-3663800	Active TSS	Colon Smooth Muscle	Colon
27	chr11:3663000-3663800	Active TSS	Fetal Brain Female	brain
28	chr11:3663000-3663800	Enhancers	Fetal Heart	heart
29	chr11:3663000-3663800	Active TSS	Fetal Intestine Small	intestine
30	chr11:3663000-3663800	Active TSS	Right Ventricle	heart
31	chr11:3663000-3663800	Active TSS	A549	lung
32	chr11:3663000-3664000	Bivalent/Poised TSS	Brain Angular Gyrus	brain
33	chr11:3663000-3664200	Active TSS	iPS-18 Cell Line	embryonic stem cell
34	chr11:3663000-3664200	Active TSS	iPS-20b Cell Line	embryonic stem cell
35	chr11:3663000-3664200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
36	chr11:3663000-3664200	Bivalent/Poised TSS	HSMM	muscle
37	chr11:3663000-3664400	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
38	chr11:3663000-3664600	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr11:3663000-3664600	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
40	chr11:3663000-3664600	Enhancers	Spleen	Spleen
41	chr11:3663200-3663600	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr11:3663200-3663600	Active TSS	Primary hematopoietic stem cells	blood
43	chr11:3663200-3663600	Active TSS	Skeletal Muscle Male	skeletal muscle
44	chr11:3663200-3663600	Active TSS	HepG2	liver
45	chr11:3663200-3663600	Active TSS	K562	blood
46	chr11:3663200-3663800	Active TSS	H1 Cell Line	embryonic stem cell
47	chr11:3663200-3663800	Bivalent/Poised TSS	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr11:3663200-3663800	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr11:3663200-3663800	Active TSS	Breast Myoepithelial Primary Cells	Breast
50	chr11:3663200-3663800	Active TSS	Fetal Intestine Large	intestine

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