Variant report

Variant	nsv879615
Chromosome Location	chr4:94100410-94180567
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	chr4:94120795-94120995	HepG2	liver:	n/a	n/a
2	ATF2	chr4:94124914-94125304	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr4:94120626-94121097	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr4:94120920-94120968	GM12878	blood:	n/a	n/a
5	CEBPB	chr4:94163240-94163557	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr4:94163354-94163550	A549	lung:	n/a	n/a
7	CEBPB	chr4:94166881-94167014	HepG2	liver:	n/a	n/a
8	CEBPB	chr4:94127343-94127543	HepG2	liver:	n/a	chr4:94127461-94127472 chr4:94127459-94127476
9	CEBPB	chr4:94138642-94138937	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr4:94152178-94152473	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr4:94152201-94152476	ECC-1	luminal epithelium:	n/a	n/a
12	CTCF	chr4:94120800-94120950	HCT-116	colon:	n/a	chr4:94120916-94120937 chr4:94120921-94120939 chr4:94120922-94120938
13	CTCF	chr4:94137419-94137442	ProgFib	skin:	n/a	n/a
14	CTCF	chr4:94120658-94121187	A549	lung:	n/a	chr4:94120916-94120937 chr4:94120921-94120939 chr4:94120922-94120938
15	CTCF	chr4:94120810-94121043	LNCaP	prostate:	n/a	chr4:94120916-94120937 chr4:94120921-94120939 chr4:94120922-94120938
16	CTCF	chr4:94120820-94120970	HCT-116	colon:	n/a	chr4:94120916-94120937 chr4:94120921-94120939 chr4:94120922-94120938
17	CTCF	chr4:94120760-94120910	HFF	foreskin:	n/a	n/a
18	CTCF	chr4:94120842-94120917	GM19240	blood:	n/a	n/a
19	CTCF	chr4:94120840-94120951	Fibrobl	skin:	n/a	chr4:94120916-94120937 chr4:94120921-94120939 chr4:94120922-94120938
20	CTCF	chr4:94120820-94120970	GM12878	blood:	n/a	chr4:94120916-94120937 chr4:94120921-94120939 chr4:94120922-94120938
21	CTCF	chr4:94159400-94159550	GM06990	blood:	n/a	n/a
22	CTCF	chr4:94120900-94121050	HL-60	blood:	n/a	chr4:94120916-94120937 chr4:94120921-94120939 chr4:94120922-94120938
23	CTCF	chr4:94120820-94120970	AG04449	skin:	n/a	chr4:94120916-94120937 chr4:94120921-94120939 chr4:94120922-94120938
24	CTCF	chr4:94120860-94121010	HEK293	kidney:	n/a	chr4:94120916-94120937 chr4:94120921-94120939 chr4:94120922-94120938
25	CTCF	chr4:94120860-94121010	HAc	cerebellar:	n/a	chr4:94120916-94120937 chr4:94120921-94120939 chr4:94120922-94120938
26	CTCF	chr4:94120860-94121010	HMEC	breast:	n/a	chr4:94120916-94120937 chr4:94120921-94120939 chr4:94120922-94120938
27	CTCF	chr4:94158842-94158872	Hela-S3	cervix:	n/a	chr4:94158849-94158870 chr4:94158854-94158872
28	CTCF	chr4:94120880-94121030	SAEC	small airway:	n/a	chr4:94120916-94120937 chr4:94120921-94120939 chr4:94120922-94120938
29	CTCF	chr4:94105383-94105522	GM12878	blood:	n/a	n/a
30	CTCF	chr4:94120832-94121038	Pancreas_OC	pancreas:	n/a	chr4:94120916-94120937 chr4:94120921-94120939 chr4:94120922-94120938
31	CTCF	chr4:94151340-94151490	AG09319	gingival:	n/a	n/a
32	CTCF	chr4:94120760-94120910	GM12865	blood:	n/a	n/a
33	CTCF	chr4:94120681-94121164	HCT-116	colon:	n/a	chr4:94120916-94120937 chr4:94120921-94120939 chr4:94120922-94120938
34	CTCF	chr4:94120820-94120970	HMEC	breast:	n/a	chr4:94120916-94120937 chr4:94120921-94120939 chr4:94120922-94120938
35	CTCF	chr4:94120848-94120966	ProgFib	skin:	n/a	chr4:94120916-94120937 chr4:94120921-94120939 chr4:94120922-94120938
36	CTCF	chr4:94120825-94121032	GM12878	blood:	n/a	chr4:94120916-94120937 chr4:94120921-94120939 chr4:94120922-94120938
37	CTCF	chr4:94120840-94120990	NHLF	lung:	n/a	chr4:94120916-94120937 chr4:94120921-94120939 chr4:94120922-94120938
38	CTCF	chr4:94120800-94120950	HRE	kidney:	n/a	chr4:94120916-94120937 chr4:94120921-94120939 chr4:94120922-94120938
39	CTCF	chr4:94120840-94120990	BJ	skin:	n/a	chr4:94120916-94120937 chr4:94120921-94120939 chr4:94120922-94120938
40	CTCF	chr4:94120820-94120970	HVMF	connective:	n/a	chr4:94120916-94120937 chr4:94120921-94120939 chr4:94120922-94120938
41	CTCF	chr4:94120840-94120990	HCPEpiC	choroid plexus:	n/a	chr4:94120916-94120937 chr4:94120921-94120939 chr4:94120922-94120938
42	CTCF	chr4:94120736-94121119	IMR90	lung:	n/a	chr4:94120916-94120937 chr4:94120921-94120939 chr4:94120922-94120938
43	CTCF	chr4:94120860-94121010	SK-N-SH_RA	brain:	n/a	chr4:94120916-94120937 chr4:94120921-94120939 chr4:94120922-94120938
44	CTCF	chr4:94120513-94121241	SK-N-SH	brain:	n/a	chr4:94120916-94120937 chr4:94120921-94120939 chr4:94120922-94120938
45	CTCF	chr4:94120881-94120989	K562	blood:	n/a	chr4:94120916-94120937 chr4:94120921-94120939 chr4:94120922-94120938
46	CTCF	chr4:94120717-94121118	A549	lung:	n/a	chr4:94120916-94120937 chr4:94120921-94120939 chr4:94120922-94120938
47	CTCF	chr4:94120793-94121012	ECC-1	luminal epithelium:	n/a	chr4:94120916-94120937 chr4:94120921-94120939 chr4:94120922-94120938
48	CTCF	chr4:94120781-94121034	MCF-7	breast:	n/a	chr4:94120916-94120937 chr4:94120921-94120939 chr4:94120922-94120938
49	CTCF	chr4:94120800-94120950	HEEpiC	esophagus:	n/a	chr4:94120916-94120937 chr4:94120921-94120939 chr4:94120922-94120938
50	CTCF	chr4:94120860-94121010	GM06990	blood:	n/a	chr4:94120916-94120937 chr4:94120921-94120939 chr4:94120922-94120938

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:94122883-94122933	MCF-7	breast:	n/a
2	chr4:94124971-94125021	AG10803	skin:	n/a
3	chr4:94122883-94122933	SAEC	small airway:	n/a
4	chr4:94125068-94125118	SK-N-SH	brain:	n/a
5	chr4:94125057-94125107	HAEpiC	amniotic membrane:	n/a
6	chr4:94124971-94125021	HIPEpiC	eye:	n/a
7	chr4:94124971-94125021	ovcar-3	ovarian:	n/a
8	chr4:94124971-94125021	HNPCEpiC	eye:	n/a
9	chr4:94122883-94122933	HCF	heart:	n/a
10	chr4:94124971-94125021	U87	brain:	n/a
11	chr4:94125057-94125107	HCPEpiC	choroid plexus:	n/a
12	chr4:94125068-94125118	ovcar-3	ovarian:	n/a
13	chr4:94124971-94125021	NB4	blood:	n/a
14	chr4:94124971-94125021	A549	lung:	n/a
15	chr4:94122883-94122933	AG09319	gingival:	n/a
16	chr4:94125057-94125107	A549	lung:	n/a
17	chr4:94124971-94125021	Caco-2	colon:	n/a
18	chr4:94125057-94125107	HEEpiC	esophagus:	n/a
19	chr4:94125057-94125107	HNPCEpiC	eye:	n/a
20	chr4:94122883-94122933	NT2-D1	testis:	n/a
21	chr4:94124971-94125021	Hela-S3	cervix:	n/a
22	chr4:94124971-94125021	GM12892	blood:	n/a
23	chr4:94125068-94125118	LNCaP	prostate:	n/a
24	chr4:94125068-94125118	PrEC	prostate:	n/a
25	chr4:94124971-94125021	CMK	blood:	n/a
26	chr4:94125068-94125118	HCM	heart:	n/a
27	chr4:94122883-94122933	AG04449	skin:	fetal
28	chr4:94125068-94125118	GM19239	blood:	n/a
29	chr4:94125068-94125118	HIPEpiC	eye:	n/a
30	chr4:94125057-94125107	HRPEpiC	eye:	n/a
31	chr4:94124971-94125021	HCF	heart:	n/a
32	chr4:94125068-94125118	SAEC	small airway:	n/a
33	chr4:94122883-94122933	ECC-1	luminal epithelium:	n/a
34	chr4:94125068-94125118	AG09319	gingival:	n/a
35	chr4:94125057-94125107	HIPEpiC	eye:	n/a
36	chr4:94125057-94125107	HCF	heart:	n/a
37	chr4:94125057-94125107	HMEC	breast:	n/a
38	chr4:94122883-94122933	HAEpiC	amniotic membrane:	n/a
39	chr4:94125057-94125107	NT2-D1	testis:	n/a
40	chr4:94125057-94125107	HCM	heart:	n/a
41	chr4:94124971-94125021	K562	blood:	n/a
42	chr4:94125068-94125118	GM12892	blood:	n/a
43	chr4:94125068-94125118	NHBE	bronchial:	n/a
44	chr4:94122883-94122933	SKMC	muscle:	n/a
45	chr4:94125057-94125107	NHBE	bronchial:	n/a
46	chr4:94122883-94122933	NH-A	brain:	n/a
47	chr4:94125057-94125107	Caco-2	colon:	n/a
48	chr4:94122883-94122933	SK-N-SH_RA	brain:	n/a
49	chr4:94122883-94122933	ProgFib	skin:	n/a
50	chr4:94122883-94122933	HUVEC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:94142565..94143188-chr4:161921512..161922366,2	MCF-7	breast:
2	chr4:94103224..94106173-chr4:94109926..94112248,2	MCF-7	breast:
3	chr4:94078923..94080034-chr4:94120388..94121356,11	MCF-7	breast:
4	chr3:17349179..17349752-chr4:94150295..94151097,2	MCF-7	breast:
5	chr4:94103224..94106173-chr4:94109926..94112248,2	MCF-7	breast:
6	chr4:94078497..94079606-chr4:94120498..94121581,4	MCF-7	breast:

Variant related genes	Relation type
GRID2	TF binding region
GRID2	CpG island

Extended variants
information (count: 2296 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:2296 , 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	rs6821061	chr4:94100410-94100411	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs532241764	chr4:94100415-94100416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs180675107	chr4:94100427-94100428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs559736020	chr4:94100452-94100453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs565859545	chr4:94100464-94100465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs114273566	chr4:94100497-94100498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs74438663	chr4:94100502-94100503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs568037030	chr4:94100518-94100519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs368859828	chr4:94100579-94100580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs536212117	chr4:94100595-94100596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs141858219	chr4:94100679-94100680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs548105291	chr4:94100680-94100681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs533151513	chr4:94100695-94100696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs539118293	chr4:94100708-94100709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs558823612	chr4:94100714-94100715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs145177633	chr4:94100727-94100728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs372488343	chr4:94100730-94100731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs572583733	chr4:94100792-94100793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs569598854	chr4:94100797-94100798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs11935709	chr4:94100807-94100808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs561534313	chr4:94100817-94100818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs575223629	chr4:94100852-94100853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs536862834	chr4:94100863-94100864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs543399993	chr4:94100884-94100885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs371852079	chr4:94100885-94100886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs532052348	chr4:94100942-94100943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs552235755	chr4:94100948-94100949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs559213728	chr4:94100950-94100951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs528245819	chr4:94100981-94100982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs547997448	chr4:94100985-94100986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs567974345	chr4:94101055-94101056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs536951291	chr4:94101057-94101058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs550649448	chr4:94101060-94101061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs558283458	chr4:94101104-94101105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs148397670	chr4:94101112-94101113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs538690935	chr4:94101125-94101126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs142529619	chr4:94101132-94101133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs150949023	chr4:94101175-94101176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs577276232	chr4:94101209-94101210	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs139528110	chr4:94101223-94101224	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs555208107	chr4:94101264-94101265	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs11945891	chr4:94101299-94101300	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs544120828	chr4:94101342-94101343	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs11936792	chr4:94101351-94101352	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs576754221	chr4:94101359-94101360	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs545506274	chr4:94101372-94101373	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs574806028	chr4:94101400-94101401	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs528183712	chr4:94101426-94101427	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs145505884	chr4:94101436-94101437	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs530405127	chr4:94101461-94101462	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
primary effusion lymphomas	17116491	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal cancer	21851588	CNVD
Cancer	19907438	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD
Autism	20841430	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Schizophrenia	23813976	CNVD
Epilepsy	20502679	CNVD

Chromatin state (count:90 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:94080600-94101200	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr4:94098400-94108000	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr4:94101200-94101600	Strong transcription	HUES48 Cell Line	embryonic stem cell
4	chr4:94101600-94119600	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr4:94103600-94105600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr4:94103800-94105600	Enhancers	NHEK	skin
7	chr4:94103800-94106200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr4:94104000-94105400	Enhancers	Stomach Mucosa	stomach
9	chr4:94104000-94105600	Enhancers	Cortex derived primary cultured neurospheres	brain
10	chr4:94104200-94104800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr4:94104400-94105400	Enhancers	Fetal Heart	heart
12	chr4:94104600-94105400	Enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr4:94104600-94105600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr4:94104600-94105600	Enhancers	HMEC	breast
15	chr4:94104800-94105800	Enhancers	Pancreatic Islets	Pancreatic Islet
16	chr4:94105200-94105600	Enhancers	Small Intestine	intestine
17	chr4:94108200-94108400	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr4:94108400-94109600	Enhancers	Fetal Brain Male	brain
19	chr4:94109200-94109600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr4:94109600-94110800	Weak transcription	Fetal Brain Male	brain
21	chr4:94110800-94111000	Enhancers	Fetal Brain Male	brain
22	chr4:94116000-94119400	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr4:94116400-94116600	Enhancers	Brain Germinal Matrix	brain
24	chr4:94116600-94117800	Weak transcription	Brain Germinal Matrix	brain
25	chr4:94117800-94118600	Enhancers	Brain Germinal Matrix	brain
26	chr4:94118600-94120200	Weak transcription	Brain Germinal Matrix	brain
27	chr4:94119200-94121200	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr4:94119400-94120800	Enhancers	H9 Cell Line	embryonic stem cell
29	chr4:94119400-94121200	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr4:94119600-94120800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr4:94119600-94120800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr4:94119600-94120800	Enhancers	Fetal Lung	lung
33	chr4:94119600-94121200	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr4:94119600-94121400	Enhancers	Fetal Stomach	stomach
35	chr4:94119800-94120400	Enhancers	iPS-20b Cell Line	embryonic stem cell
36	chr4:94119800-94121200	Enhancers	H1 Cell Line	embryonic stem cell
37	chr4:94120200-94120400	Enhancers	Brain Germinal Matrix	brain
38	chr4:94120200-94120800	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr4:94120200-94121200	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr4:94120400-94120800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
41	chr4:94120400-94120800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr4:94120400-94120800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
43	chr4:94120400-94121200	Enhancers	HUES64 Cell Line	embryonic stem cell
44	chr4:94120600-94120800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr4:94120600-94120800	Enhancers	Liver	Liver
46	chr4:94120800-94121200	Enhancers	iPS-20b Cell Line	embryonic stem cell
47	chr4:94120800-94122600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
48	chr4:94120800-94124800	Weak transcription	H9 Cell Line	embryonic stem cell
49	chr4:94120800-94130800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr4:94121200-94122400	Weak transcription	iPS-18 Cell Line	embryonic stem cell

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