Variant report

Variant	nsv1039186
Chromosome Location	chr11:4563343-4598185
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:262)
CpG islands
(count:489)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:262 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:4568278-4568297	HepG2	liver:	n/a	n/a
2	BACH1	chr11:4580944-4580984	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr11:4578528-4578549	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr11:4569325-4569525	A549	lung:	n/a	chr11:4569397-4569410
5	CEBPB	chr11:4568337-4568455	HepG2	liver:	n/a	n/a
6	CHD1	chr11:4591087-4591112	H1-hESC	embryonic stem cell:	n/a	n/a
7	CTCF	chr11:4572822-4573161	H1-hESC	embryonic stem cell:	n/a	n/a
8	CTCF	chr11:4572920-4573070	HEK293	kidney:	n/a	n/a
9	CTCF	chr11:4572920-4573070	HPF	lung:	n/a	n/a
10	CTCF	chr11:4572920-4573070	HRE	kidney:	n/a	n/a
11	CTCF	chr11:4572960-4573110	HPAF	blood vessel:	n/a	n/a
12	CTCF	chr11:4572920-4573070	BJ	skin:	n/a	n/a
13	CTCF	chr11:4572920-4573070	AG09319	gingival:	n/a	n/a
14	CTCF	chr11:4572940-4573090	HUVEC	blood vessel:	n/a	n/a
15	CTCF	chr11:4572920-4573070	SAEC	small airway:	n/a	n/a
16	CTCF	chr11:4572900-4573050	HUVEC	blood vessel:	n/a	n/a
17	CTCF	chr11:4583883-4583944	GM20000	blood:	n/a	n/a
18	CTCF	chr11:4572916-4573130	GM12878	blood:	n/a	n/a
19	CTCF	chr11:4572940-4573090	GM12868	blood:	n/a	n/a
20	CTCF	chr11:4572920-4573070	GM12870	blood:	n/a	n/a
21	CTCF	chr11:4572940-4573090	GM12874	blood:	n/a	n/a
22	CTCF	chr11:4572960-4573110	AG09309	skin:	n/a	n/a
23	CTCF	chr11:4572940-4573090	AoAF	blood vessel:	n/a	n/a
24	CTCF	chr11:4572923-4573080	SK-N-SH_RA	brain:	n/a	n/a
25	CTCF	chr11:4573317-4573336	GM12892	blood:	n/a	n/a
26	CTCF	chr11:4572960-4573110	AG04450	lung:	n/a	n/a
27	CTCF	chr11:4572960-4573110	SAEC	small airway:	n/a	n/a
28	CTCF	chr11:4573000-4573150	A549	lung:	n/a	n/a
29	CTCF	chr11:4572960-4573110	HFF-Myc	foreskin:	n/a	n/a
30	CTCF	chr11:4572949-4573099	MCF-7	breast:	n/a	n/a
31	CTCF	chr11:4572960-4573110	A549	lung:	n/a	n/a
32	CTCF	chr11:4572880-4573030	K562	blood:	n/a	n/a
33	CTCF	chr11:4572820-4572970	GM12868	blood:	n/a	n/a
34	CTCF	chr11:4572900-4573050	RPTEC	kidney:	n/a	n/a
35	CTCF	chr11:4572980-4573130	NHEK	skin:	n/a	n/a
36	CTCF	chr11:4573040-4573190	HL-60	blood:	n/a	n/a
37	CTCF	chr11:4572940-4573090	HRPEpiC	eye:	n/a	n/a
38	CTCF	chr11:4572940-4573090	GM12875	blood:	n/a	n/a
39	CTCF	chr11:4572920-4573070	HFF-Myc	foreskin:	n/a	n/a
40	CTCF	chr11:4572672-4572808	GM12892	blood:	n/a	n/a
41	CTCF	chr11:4572920-4573070	Caco-2	colon:	n/a	n/a
42	CTCF	chr11:4572999-4573093	GM10248	blood:	n/a	n/a
43	CTCF	chr11:4572940-4573090	GM12870	blood:	n/a	n/a
44	CTCF	chr11:4573285-4573354	GM12878	blood:	n/a	n/a
45	CTCF	chr11:4573000-4573150	HCT-116	colon:	n/a	n/a
46	CTCF	chr11:4572920-4573070	K562	blood:	n/a	n/a
47	CTCF	chr11:4572878-4573190	IMR90	lung:	n/a	n/a
48	CTCF	chr11:4572960-4573110	GM12878	blood:	n/a	n/a
49	CTCF	chr11:4572915-4573135	SK-N-SH_RA	brain:	n/a	n/a
50	CTCF	chr11:4572940-4573132	A549	lung:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:4565475-4565525	MCF-7	breast:	n/a
2	chr11:4565475-4565525	MCF-7	breast:	n/a
3	chr11:4590491-4590541	HEK293	kidney:	embryo
4	chr11:4590536-4590586	NB4	blood:	n/a
5	chr11:4566380-4566430	AG09309	skin:	n/a
6	chr11:4590491-4590541	Hepatocyte	liver:	n/a
7	chr11:4566169-4566219	ovcar-3	ovarian:	n/a
8	chr11:4566853-4566903	RPTEC	kidney:	n/a
9	chr11:4597246-4597296	HUVEC	blood vessel:	n/a
10	chr11:4590536-4590586	HMEC	breast:	n/a
11	chr11:4565489-4565539	GM12878	blood:	n/a
12	chr11:4565489-4565539	T-47D	breast:	n/a
13	chr11:4565475-4565525	HAEpiC	amniotic membrane:	n/a
14	chr11:4597246-4597296	GM19239	blood:	n/a
15	chr11:4565489-4565539	HIPEpiC	eye:	n/a
16	chr11:4566380-4566430	HepG2	liver:	n/a
17	chr11:4566380-4566430	IMR90	lung:	fetal
18	chr11:4565489-4565539	ovcar-3	ovarian:	n/a
19	chr11:4566380-4566430	PFSK-1	brain:	n/a
20	chr11:4597246-4597296	Hepatocyte	liver:	n/a
21	chr11:4565489-4565539	AoSMC	blood vessel:	n/a
22	chr11:4590491-4590541	CMK	blood:	n/a
23	chr11:4566380-4566430	HRPEpiC	eye:	n/a
24	chr11:4565489-4565539	U87	brain:	n/a
25	chr11:4590536-4590586	HRE	kidney:	n/a
26	chr11:4590491-4590541	AG10803	skin:	n/a
27	chr11:4566169-4566219	HRE	kidney:	n/a
28	chr11:4566169-4566219	SK-N-MC	brain:	n/a
29	chr11:4566853-4566903	U87	brain:	n/a
30	chr11:4597246-4597296	NT2-D1	testis:	n/a
31	chr11:4566853-4566903	PFSK-1	brain:	n/a
32	chr11:4566853-4566903	CMK	blood:	n/a
33	chr11:4590536-4590586	HEEpiC	esophagus:	n/a
34	chr11:4566169-4566219	Hela-S3	cervix:	n/a
35	chr11:4566853-4566903	IMR90	lung:	fetal
36	chr11:4590536-4590586	LNCaP	prostate:	n/a
37	chr11:4566380-4566430	MCF-7	breast:	n/a
38	chr11:4590491-4590541	RPTEC	kidney:	n/a
39	chr11:4566169-4566219	HMEC	breast:	n/a
40	chr11:4590491-4590541	HCM	heart:	n/a
41	chr11:4566380-4566430	ProgFib	skin:	n/a
42	chr11:4590491-4590541	GM12878	blood:	n/a
43	chr11:4590491-4590541	AoSMC	blood vessel:	n/a
44	chr11:4566380-4566430	AoSMC	blood vessel:	n/a
45	chr11:4565489-4565539	AG10803	skin:	n/a
46	chr11:4565489-4565539	HL-60	blood:	n/a
47	chr11:4565489-4565539	HAEpiC	amniotic membrane:	n/a
48	chr11:4565489-4565539	SK-N-SH_RA	brain:	n/a
49	chr11:4566169-4566219	HL-60	blood:	n/a
50	chr11:4566853-4566903	NHBE	bronchial:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:4563397..4564933-chr11:4566554..4568624,2	K562	blood:
2	chr1:45195876..45196736-chr11:4594433..4595433,5	Hela-S3	cervix:
3	chr11:4208891..4209471-chr11:4572771..4573597,3	MCF-7	breast:
4	chr11:4558523..4560457-chr11:4563023..4565124,2	K562	blood:
5	chr11:4208647..4209327-chr11:4572350..4573087,2	MCF-7	breast:
6	chr11:4575133..4577035-chr11:4578318..4580954,2	K562	blood:
7	chr11:4575133..4577035-chr11:4578318..4580954,2	K562	blood:
8	chr11:4563397..4564933-chr11:4566554..4568624,2	K562	blood:
9	chr11:4563433..4564999-chr11:4565844..4568054,2	K562	blood:

No data

Variant related genes	Relation type
OR52M1	TF binding region
OR52M1	CpG island
ENSG00000197790	chromatin interactions

Extended variants
information (count: 2269 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:2269 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2566272	chr11:4563436-4563437	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs149616107	chr11:4563467-4563468	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs529172874	chr11:4563470-4563471	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs182870403	chr11:4563471-4563472	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs569034600	chr11:4563485-4563486	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs80145084	chr11:4563505-4563506	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs113288539	chr11:4563531-4563532	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs2657170	chr11:4563590-4563591	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs570835444	chr11:4563606-4563607	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs535153337	chr11:4563625-4563626	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs369221385	chr11:4563641-4563642	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs188334835	chr11:4563660-4563661	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs2641413	chr11:4563675-4563676	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs191323767	chr11:4563681-4563682	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs557240158	chr11:4563688-4563689	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs575396615	chr11:4563689-4563690	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs146839036	chr11:4563698-4563699	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs140718924	chr11:4563727-4563728	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs17220520	chr11:4563728-4563729	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs569677960	chr11:4563737-4563738	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs182190792	chr11:4563755-4563756	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs532223750	chr11:4563763-4563764	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs561479329	chr11:4563779-4563780	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs145858768	chr11:4563819-4563820	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs371014987	chr11:4563821-4563822	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs146560900	chr11:4563843-4563844	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs201014635	chr11:4563860-4563861	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs6578498	chr11:4563901-4563902	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs78735276	chr11:4563926-4563927	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs150228023	chr11:4563965-4563966	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs535127631	chr11:4563992-4563993	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs138819306	chr11:4564002-4564003	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs186976439	chr11:4564012-4564013	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs534833787	chr11:4564015-4564016	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs192492555	chr11:4564020-4564021	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs568321730	chr11:4564024-4564025	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs12290576	chr11:4564033-4564034	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs557201477	chr11:4564048-4564049	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs569193887	chr11:4564050-4564051	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs376697782	chr11:4564059-4564060	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs539787114	chr11:4564060-4564061	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs2566271	chr11:4564086-4564087	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs184921593	chr11:4564087-4564088	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs537398433	chr11:4564102-4564103	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs555456429	chr11:4564143-4564144	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs556262404	chr11:4564144-4564145	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs2709127	chr11:4564158-4564159	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs545067527	chr11:4564160-4564161	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs2657169	chr11:4564187-4564188	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs115853805	chr11:4564191-4564192	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Neuroblastoma	18923191	CNVD
Breast cancer	19432969	CNVD
Alzheimer''s disease	17576883	CNVD
Long-qt syndrome	17576883	CNVD
Emphysema	19352772	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chordoma	18071362	CNVD
Breast cancer	16608533	CNVD
Cancer	21183584	CNVD
Gastric adenocarcinoma	19115996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Myelofibrosis	22110671	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Neuroblastoma	21124317	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Schizophrenia	21399695	CNVD
Gastric cancer	16891809	CNVD
Cancer	17160897	CNVD
Multiple myeloma	16616336	CNVD
small cell lung cancer	20016488	CNVD
Bipolar disorder	19114987	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Pancreatic cancer	23613489	CNVD

Chromatin state (count:63 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:4564600-4565200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr11:4564600-4565200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr11:4564600-4565400	Enhancers	HUVEC	blood vessel
4	chr11:4564600-4565400	Enhancers	NHEK	skin
5	chr11:4564800-4565200	Enhancers	A549	lung
6	chr11:4564800-4565400	Enhancers	HMEC	breast
7	chr11:4566600-4569800	Enhancers	Liver	Liver
8	chr11:4567200-4568800	Enhancers	Sigmoid Colon	Sigmoid Colon
9	chr11:4567600-4569400	Enhancers	Pancreatic Islets	Pancreatic Islet
10	chr11:4567800-4569200	Enhancers	Fetal Intestine Small	intestine
11	chr11:4567800-4569400	Enhancers	Fetal Intestine Large	intestine
12	chr11:4568000-4568400	Enhancers	Stomach Mucosa	stomach
13	chr11:4568000-4569400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr11:4568400-4568600	Enhancers	Gastric	stomach
15	chr11:4568600-4569200	Enhancers	Small Intestine	intestine
16	chr11:4568600-4580600	Weak transcription	Gastric	stomach
17	chr11:4572000-4572400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr11:4572400-4572600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr11:4572600-4572800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr11:4575200-4575600	Enhancers	K562	blood
21	chr11:4580400-4581600	Enhancers	Pancreas	Pancrea
22	chr11:4580400-4582600	Enhancers	Placenta	Placenta
23	chr11:4580600-4581200	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr11:4580600-4581400	Enhancers	Esophagus	oesophagus
25	chr11:4580600-4581600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr11:4580600-4581600	Enhancers	Gastric	stomach
27	chr11:4580800-4581600	Enhancers	Fetal Lung	lung
28	chr11:4580800-4581800	Enhancers	Fetal Intestine Large	intestine
29	chr11:4580800-4581800	Enhancers	Fetal Intestine Small	intestine
30	chr11:4580800-4582000	Enhancers	Placenta Amnion	Placenta Amnion
31	chr11:4581000-4581200	Flanking Active TSS	Colonic Mucosa	Colon
32	chr11:4581000-4581400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr11:4581000-4581400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr11:4581000-4581400	Enhancers	Breast Myoepithelial Primary Cells	Breast
35	chr11:4581000-4581800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr11:4581000-4582000	Enhancers	Duodenum Mucosa	Duodenum
37	chr11:4581200-4581400	Active TSS	Colonic Mucosa	Colon
38	chr11:4581200-4582000	Enhancers	Stomach Mucosa	stomach
39	chr11:4586400-4588400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
40	chr11:4586600-4588600	Enhancers	Adipose Nuclei	Adipose
41	chr11:4586800-4588600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr11:4590400-4590600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr11:4592400-4593400	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr11:4592600-4593600	Enhancers	H1 Cell Line	embryonic stem cell
45	chr11:4592600-4593600	Enhancers	H9 Cell Line	embryonic stem cell
46	chr11:4592800-4593000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
47	chr11:4592800-4593200	Enhancers	iPS-20b Cell Line	embryonic stem cell
48	chr11:4592800-4593600	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr11:4592800-4593600	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr11:4592800-4593800	Enhancers	iPS-18 Cell Line	embryonic stem cell

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