Variant report

Variant	nsv1013515
Chromosome Location	chr3:155065109-155095455
allele	n/a
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	ARID3A	chr3:155088990-155089244	K562	blood:	n/a	n/a
2	ARID3A	chr3:155070719-155071096	K562	blood:	n/a	n/a
3	ATF1	chr3:155088896-155089368	K562	blood:	n/a	n/a
4	ATF2	chr3:155080866-155081756	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr3:155080911-155081858	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr3:155087030-155087448	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL11A	chr3:155081109-155081484	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL11A	chr3:155080891-155081495	H1-hESC	embryonic stem cell:	n/a	n/a
9	BHLHE40	chr3:155081668-155081910	GM12878	blood:	n/a	n/a
10	BRCA1	chr3:155074518-155074581	GM12878	blood:	n/a	n/a
11	CBX3	chr3:155082992-155083262	K562	blood:	n/a	n/a
12	CBX3	chr3:155082942-155083412	HCT-116	colon:	n/a	n/a
13	CEBPB	chr3:155081051-155081313	K562	blood:	n/a	chr3:155081220-155081231
14	CEBPB	chr3:155080744-155081738	H1-hESC	embryonic stem cell:	n/a	chr3:155081220-155081231
15	CEBPB	chr3:155081073-155081387	A549	lung:	n/a	chr3:155081220-155081231
16	CEBPB	chr3:155081057-155081400	Hela-S3	cervix:	n/a	chr3:155081220-155081231
17	CEBPB	chr3:155080994-155081528	ECC-1	luminal epithelium:	n/a	chr3:155081220-155081231
18	CEBPB	chr3:155071939-155072209	IMR90	lung:	n/a	n/a
19	CEBPB	chr3:155088957-155089185	K562	blood:	n/a	n/a
20	CEBPB	chr3:155081014-155081531	ECC-1	luminal epithelium:	n/a	chr3:155081220-155081231
21	CEBPB	chr3:155081060-155081402	HepG2	liver:	n/a	chr3:155081220-155081231
22	CEBPB	chr3:155081026-155081426	K562	blood:	n/a	chr3:155081220-155081231
23	CEBPB	chr3:155081001-155081421	K562	blood:	n/a	chr3:155081220-155081231
24	CEBPB	chr3:155072646-155072734	HepG2	liver:	n/a	n/a
25	CEBPB	chr3:155081045-155081393	IMR90	lung:	n/a	chr3:155081220-155081231
26	CEBPB	chr3:155071926-155072179	HepG2	liver:	n/a	n/a
27	CHD1	chr3:155083157-155083173	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr3:155080885-155081683	H1-hESC	embryonic stem cell:	n/a	n/a
29	CREB1	chr3:155080979-155081545	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTBP2	chr3:155080992-155081480	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr3:155074480-155074630	GM12874	blood:	n/a	n/a
32	CTCF	chr3:155070860-155071010	NHDF-neo	bronchial:	n/a	chr3:155070880-155070896 chr3:155070884-155070892 chr3:155070879-155070897 chr3:155070881-155070902
33	CTCF	chr3:155070800-155070950	GM12874	blood:	n/a	chr3:155070880-155070896 chr3:155070884-155070892 chr3:155070879-155070897 chr3:155070881-155070902
34	CTCF	chr3:155074500-155074650	GM12873	blood:	n/a	n/a
35	CTCF	chr3:155074531-155074563	LNCaP	prostate:	n/a	n/a
36	CTCF	chr3:155070840-155070990	NHLF	lung:	n/a	chr3:155070880-155070896 chr3:155070884-155070892 chr3:155070879-155070897 chr3:155070881-155070902
37	CTCF	chr3:155070716-155071067	K562	blood:	n/a	chr3:155070880-155070896 chr3:155070884-155070892 chr3:155070879-155070897 chr3:155070881-155070902
38	CTCF	chr3:155074417-155074666	MCF-7	breast:	n/a	n/a
39	CTCF	chr3:155074422-155074659	MCF-7	breast:	n/a	n/a
40	CTCF	chr3:155074480-155074630	AoAF	blood vessel:	n/a	n/a
41	CTCF	chr3:155070840-155070990	GM12871	blood:	n/a	chr3:155070880-155070896 chr3:155070884-155070892 chr3:155070879-155070897 chr3:155070881-155070902
42	CTCF	chr3:155070775-155070979	Lung_OC	lung:	n/a	chr3:155070880-155070896 chr3:155070884-155070892 chr3:155070879-155070897 chr3:155070881-155070902
43	CTCF	chr3:155074400-155074550	HEK293	kidney:	n/a	n/a
44	CTCF	chr3:155070820-155070970	HA-sp	spinal cord:	n/a	chr3:155070880-155070896 chr3:155070884-155070892 chr3:155070879-155070897 chr3:155070881-155070902
45	CTCF	chr3:155070838-155070948	GM10266	blood:	n/a	chr3:155070880-155070896 chr3:155070884-155070892 chr3:155070879-155070897 chr3:155070881-155070902
46	CTCF	chr3:155070780-155070930	AoAF	blood vessel:	n/a	chr3:155070880-155070896 chr3:155070884-155070892 chr3:155070879-155070897 chr3:155070881-155070902
47	CTCF	chr3:155070766-155070975	LNCaP	prostate:	n/a	chr3:155070880-155070896 chr3:155070884-155070892 chr3:155070879-155070897 chr3:155070881-155070902
48	CTCF	chr3:155074474-155074622	NHEK	skin:	n/a	n/a
49	CTCF	chr3:155070880-155071030	GM12865	blood:	n/a	chr3:155070880-155070896 chr3:155070884-155070892 chr3:155070881-155070902
50	CTCF	chr3:155074458-155074606	GM19239	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:155088879-155088929	HPAEpiC	pulmonary alveolar:	n/a
2	chr3:155088879-155088929	Hepatocyte	liver:	n/a
3	chr3:155088879-155088929	K562	blood:	n/a
4	chr3:155088879-155088929	IMR90	lung:	fetal
5	chr3:155088879-155088929	HRPEpiC	eye:	n/a
6	chr3:155088879-155088929	GM12878	blood:	n/a
7	chr3:155088879-155088929	HCM	heart:	n/a
8	chr3:155088879-155088929	HNPCEpiC	eye:	n/a
9	chr3:155088879-155088929	HUVEC	blood vessel:	n/a
10	chr3:155088879-155088929	NB4	blood:	n/a
11	chr3:155088879-155088929	LNCaP	prostate:	n/a
12	chr3:155088879-155088929	ovcar-3	ovarian:	n/a
13	chr3:155088879-155088929	MCF10A-Er-Src	breast:	n/a
14	chr3:155088879-155088929	HL-60	blood:	n/a
15	chr3:155088879-155088929	HRE	kidney:	n/a
16	chr3:155088879-155088929	NT2-D1	testis:	n/a
17	chr3:155088879-155088929	H1-hESC	embryonic stem cell:	embryo
18	chr3:155088879-155088929	A549	lung:	n/a
19	chr3:155088879-155088929	T-47D	breast:	n/a
20	chr3:155088879-155088929	PrEC	prostate:	n/a
21	chr3:155088879-155088929	PANC-1	pancreas:	n/a
22	chr3:155088879-155088929	HCF	heart:	n/a
23	chr3:155088879-155088929	SK-N-SH_RA	brain:	n/a
24	chr3:155088879-155088929	HMEC	breast:	n/a
25	chr3:155088879-155088929	NHDF-neo	bronchial:	n/a
26	chr3:155088879-155088929	CMK	blood:	n/a
27	chr3:155088879-155088929	GM19239	blood:	n/a
28	chr3:155088879-155088929	GM12891	blood:	n/a
29	chr3:155088879-155088929	BJ	skin:	n/a
30	chr3:155088879-155088929	AG04449	skin:	fetal
31	chr3:155088879-155088929	HEK293	kidney:	embryo
32	chr3:155088879-155088929	Caco-2	colon:	n/a
33	chr3:155088879-155088929	HRCEpiC	kidney:	n/a
34	chr3:155088879-155088929	BE2_C	brain:	n/a
35	chr3:155088879-155088929	Hela-S3	cervix:	n/a
36	chr3:155088879-155088929	HEEpiC	esophagus:	n/a
37	chr3:155088879-155088929	GM12892	blood:	n/a
38	chr3:155088879-155088929	GM06990	blood:	n/a
39	chr3:155088879-155088929	HCPEpiC	choroid plexus:	n/a
40	chr3:155088879-155088929	U87	brain:	n/a
41	chr3:155088879-155088929	Jurkat	blood:	n/a
42	chr3:155088879-155088929	SAEC	small airway:	n/a
43	chr3:155088879-155088929	ProgFib	skin:	n/a
44	chr3:155088879-155088929	AG04450	lung:	fetal
45	chr3:155088879-155088929	HepG2	liver:	n/a
46	chr3:155088879-155088929	ECC-1	luminal epithelium:	n/a
47	chr3:155088879-155088929	RPTEC	kidney:	n/a
48	chr3:155088879-155088929	SK-N-MC	brain:	n/a
49	chr3:155088879-155088929	HCT-116	colon:	n/a
50	chr3:155088879-155088929	MCF-7	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:155083019..155084599-chr3:155087307..155088949,2	MCF-7	breast:
2	chr3:155074075..155074622-chr3:155419261..155420274,3	K562	blood:
3	chr3:155076882..155078450-chr3:155086803..155088719,2	K562	blood:
4	chr3:155072085..155073011-chr3:155419476..155420067,2	MCF-7	breast:
5	chr3:155070862..155073357-chr3:155073807..155076267,2	K562	blood:
6	chr3:155070862..155073357-chr3:155073807..155076267,2	K562	blood:
7	chr3:155070467..155071395-chr3:155419423..155420352,4	K562	blood:
8	chr3:155070527..155071479-chr3:155419274..155420293,4	MCF-7	breast:
9	chr3:155074208..155074956-chr3:155419567..155420189,2	MCF-7	breast:
10	chr3:155083019..155084599-chr3:155087307..155088949,2	MCF-7	breast:
11	chr3:155050997..155053390-chr3:155063362..155066167,2	K562	blood:
12	chr18:64948798..64949652-chr3:155070443..155071034,2	MCF-7	breast:
13	chr3:155075914..155077862-chr3:155419961..155422752,2	K562	blood:
14	chr3:155076882..155078450-chr3:155086803..155088719,2	K562	blood:

Variant related genes	Relation type
ENSG00000248772	TF binding region
ENSG00000248772	CpG island
ENSG00000114805	chromatin interactions

Extended variants
information (count: 916 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs537763480	chr3:155065157-155065158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs549756645	chr3:155065158-155065159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs188161846	chr3:155065220-155065221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs567788752	chr3:155065290-155065291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs191843740	chr3:155065324-155065325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs546103317	chr3:155065325-155065326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs559982407	chr3:155065390-155065391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs572206477	chr3:155065411-155065412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs543224614	chr3:155065522-155065523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs561491786	chr3:155065547-155065548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs370508061	chr3:155065592-155065593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs370391042	chr3:155065649-155065650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs532011113	chr3:155065650-155065651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs550218644	chr3:155065651-155065652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs150037763	chr3:155065700-155065701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs373655663	chr3:155065704-155065705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs116102944	chr3:155065708-155065709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs547801710	chr3:155065709-155065710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs62276899	chr3:155065711-155065712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs536368867	chr3:155065757-155065758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs73172435	chr3:155065784-155065785	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs572838763	chr3:155070432-155070433	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs6440974	chr3:155070465-155070466	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs140141119	chr3:155070501-155070502	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs6440975	chr3:155070591-155070592	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs188848574	chr3:155070596-155070597	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs35189564	chr3:155070612-155070613	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs543972401	chr3:155070647-155070648	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs145355997	chr3:155070670-155070671	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs376395389	chr3:155070704-155070705	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs544458757	chr3:155070747-155070748	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs533352676	chr3:155070775-155070776	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs552037784	chr3:155070781-155070782	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs532421058	chr3:155072243-155072244	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs547480794	chr3:155072248-155072249	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs530771500	chr3:155072273-155072274	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs140375358	chr3:155072281-155072282	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs186027655	chr3:155072310-155072311	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs527466144	chr3:155072338-155072339	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs549188332	chr3:155072355-155072356	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs150302290	chr3:155072358-155072359	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs538158896	chr3:155072386-155072387	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs137933650	chr3:155072410-155072411	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs571225905	chr3:155072439-155072440	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs538685483	chr3:155072454-155072455	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs78144402	chr3:155072494-155072495	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs572206741	chr3:155072511-155072512	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs550314603	chr3:155072587-155072588	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs543224500	chr3:155072591-155072592	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs555168920	chr3:155072650-155072651	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	21115979	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Hepatocellular carcinoma	16750200	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21364760	CNVD
Basal cell lymphoma	17170743	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	16608533	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-small cell lung cancer	19010865	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Neurodevelopmental disorder	22521361	CNVD
Bladder cancer	21909424	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Cancer	17440070	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16547154	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:234 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:155054800-155065800	Weak transcription	K562	blood
2	chr3:155070400-155070800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr3:155070400-155070800	Enhancers	Primary hematopoietic stem cells short term culture	blood
4	chr3:155070600-155070800	Enhancers	Brain Angular Gyrus	brain
5	chr3:155072200-155073200	Enhancers	Liver	Liver
6	chr3:155072200-155073200	Enhancers	HepG2	liver
7	chr3:155072400-155073000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr3:155072400-155073000	Enhancers	Fetal Intestine Small	intestine
9	chr3:155072400-155073000	Enhancers	HMEC	breast
10	chr3:155072600-155073200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr3:155073000-155073800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr3:155073200-155074200	Weak transcription	HepG2	liver
13	chr3:155073200-155081400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr3:155073800-155074000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr3:155074200-155074400	Enhancers	HepG2	liver
16	chr3:155074200-155075200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr3:155074200-155076200	Enhancers	H1 Cell Line	embryonic stem cell
18	chr3:155074400-155075800	Enhancers	H9 Cell Line	embryonic stem cell
19	chr3:155074400-155075800	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr3:155074400-155076000	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr3:155074600-155074800	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr3:155074600-155074800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
23	chr3:155074600-155075000	Enhancers	Brain Cingulate Gyrus	brain
24	chr3:155074600-155075200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr3:155074600-155075800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
26	chr3:155074600-155075800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
27	chr3:155074600-155075800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr3:155074600-155076000	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr3:155074600-155076000	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr3:155075000-155075200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr3:155075000-155075800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
32	chr3:155075200-155079200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr3:155075200-155079400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr3:155075200-155080800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr3:155075600-155075800	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr3:155076000-155078000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
37	chr3:155077200-155078600	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr3:155077200-155079000	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
39	chr3:155077600-155078000	Enhancers	H9 Cell Line	embryonic stem cell
40	chr3:155077600-155078200	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr3:155077600-155079800	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
42	chr3:155077800-155078800	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr3:155077800-155080000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
44	chr3:155078000-155078600	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr3:155078400-155078600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
46	chr3:155078600-155078800	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
47	chr3:155078600-155079800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
48	chr3:155078800-155079800	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
49	chr3:155079000-155080000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
50	chr3:155079200-155079800	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell

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