Variant report

Variant	nsv537092
Chromosome Location	chr4:53338708-53436560
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	chr4:53411648-53411870	HepG2	liver:	n/a	n/a
2	ATF3	chr4:53418990-53419249	K562	blood:	n/a	n/a
3	BCLAF1	chr4:53411513-53412027	GM12878	blood:	n/a	chr4:53411696-53411709
4	BHLHE40	chr4:53411571-53411923	K562	blood:	n/a	n/a
5	BHLHE40	chr4:53411635-53411951	GM12878	blood:	n/a	n/a
6	CCNT2	chr4:53418972-53419303	K562	blood:	n/a	n/a
7	CEBPB	chr4:53403533-53403649	A549	lung:	n/a	chr4:53403551-53403562
8	CEBPB	chr4:53346626-53346661	IMR90	lung:	n/a	n/a
9	CEBPB	chr4:53403451-53403620	HepG2	liver:	n/a	chr4:53403551-53403562
10	CEBPB	chr4:53426877-53427559	IMR90	lung:	n/a	n/a
11	CEBPB	chr4:53432325-53433093	IMR90	lung:	n/a	n/a
12	CEBPB	chr4:53403557-53403602	K562	blood:	n/a	n/a
13	CHD2	chr4:53419112-53419222	Hela-S3	cervix:	n/a	n/a
14	CHD2	chr4:53411690-53411931	GM12878	blood:	n/a	n/a
15	CTCF	chr4:53396240-53396390	HCT-116	colon:	n/a	n/a
16	CTCF	chr4:53411700-53411850	Caco-2	colon:	n/a	chr4:53411796-53411817 chr4:53411797-53411810 chr4:53411794-53411812
17	CTCF	chr4:53411671-53411942	A549	lung:	n/a	chr4:53411796-53411817 chr4:53411797-53411810 chr4:53411794-53411812
18	CTCF	chr4:53411599-53411925	H1-hESC	embryonic stem cell:	n/a	chr4:53411796-53411817 chr4:53411797-53411810 chr4:53411794-53411812
19	CTCF	chr4:53411780-53411930	NHDF-neo	bronchial:	n/a	chr4:53411796-53411817 chr4:53411797-53411810 chr4:53411794-53411812
20	CTCF	chr4:53411740-53411890	AoAF	blood vessel:	n/a	chr4:53411796-53411817 chr4:53411797-53411810 chr4:53411794-53411812
21	CTCF	chr4:53411720-53411870	Caco-2	colon:	n/a	chr4:53411796-53411817 chr4:53411797-53411810 chr4:53411794-53411812
22	CTCF	chr4:53411680-53411830	AG04450	lung:	n/a	chr4:53411796-53411817 chr4:53411797-53411810 chr4:53411794-53411812
23	CTCF	chr4:53411740-53411890	HPAF	blood vessel:	n/a	chr4:53411796-53411817 chr4:53411797-53411810 chr4:53411794-53411812
24	CTCF	chr4:53411438-53411503	ProgFib	skin:	n/a	n/a
25	CTCF	chr4:53411720-53411870	GM12866	blood:	n/a	chr4:53411796-53411817 chr4:53411797-53411810 chr4:53411794-53411812
26	CTCF	chr4:53411642-53411936	Kidney_OC	kidney:	n/a	chr4:53411796-53411817 chr4:53411797-53411810 chr4:53411794-53411812
27	CTCF	chr4:53411619-53411949	SK-N-SH_RA	brain:	n/a	chr4:53411796-53411817 chr4:53411797-53411810 chr4:53411794-53411812
28	CTCF	chr4:53411674-53411921	K562	blood:	n/a	chr4:53411796-53411817 chr4:53411797-53411810 chr4:53411794-53411812
29	CTCF	chr4:53411659-53411983	ECC-1	luminal epithelium:	n/a	chr4:53411796-53411817 chr4:53411797-53411810 chr4:53411794-53411812
30	CTCF	chr4:53411669-53411931	GM10248	blood:	n/a	chr4:53411796-53411817 chr4:53411797-53411810 chr4:53411794-53411812
31	CTCF	chr4:53411740-53411890	HVMF	connective:	n/a	chr4:53411796-53411817 chr4:53411797-53411810 chr4:53411794-53411812
32	CTCF	chr4:53411628-53411938	GM19239	blood:	n/a	chr4:53411796-53411817 chr4:53411797-53411810 chr4:53411794-53411812
33	CTCF	chr4:53411519-53411525	Gliobla	brain:	n/a	n/a
34	CTCF	chr4:53411666-53411913	Hela-S3	cervix:	n/a	chr4:53411796-53411817 chr4:53411797-53411810 chr4:53411794-53411812
35	CTCF	chr4:53411700-53411850	GM12867	blood:	n/a	chr4:53411796-53411817 chr4:53411797-53411810 chr4:53411794-53411812
36	CTCF	chr4:53344279-53344320	GM20000	blood:	n/a	n/a
37	CTCF	chr4:53411700-53411850	GM12865	blood:	n/a	chr4:53411796-53411817 chr4:53411797-53411810 chr4:53411794-53411812
38	CTCF	chr4:53411653-53411955	Medullo	brain:	n/a	chr4:53411796-53411817 chr4:53411797-53411810 chr4:53411794-53411812
39	CTCF	chr4:53411700-53411850	GM12875	blood:	n/a	chr4:53411796-53411817 chr4:53411797-53411810 chr4:53411794-53411812
40	CTCF	chr4:53424906-53424932	GM13976	blood:	n/a	n/a
41	CTCF	chr4:53411593-53412151	K562	blood:	n/a	chr4:53411796-53411817 chr4:53411797-53411810 chr4:53411794-53411812
42	CTCF	chr4:53411720-53411870	NHEK	skin:	n/a	chr4:53411796-53411817 chr4:53411797-53411810 chr4:53411794-53411812
43	CTCF	chr4:53411760-53411910	HCT-116	colon:	n/a	chr4:53411796-53411817 chr4:53411797-53411810 chr4:53411794-53411812
44	CTCF	chr4:53411700-53411850	HVMF	connective:	n/a	chr4:53411796-53411817 chr4:53411797-53411810 chr4:53411794-53411812
45	CTCF	chr4:53411681-53411929	T-47D	breast:	n/a	chr4:53411796-53411817 chr4:53411797-53411810 chr4:53411794-53411812
46	CTCF	chr4:53411740-53411890	GM06990	blood:	n/a	chr4:53411796-53411817 chr4:53411797-53411810 chr4:53411794-53411812
47	CTCF	chr4:53411740-53411890	GM12871	blood:	n/a	chr4:53411796-53411817 chr4:53411797-53411810 chr4:53411794-53411812
48	CTCF	chr4:53411720-53411870	HMF	breast:	n/a	chr4:53411796-53411817 chr4:53411797-53411810 chr4:53411794-53411812
49	CTCF	chr4:53411635-53411947	NHEK	skin:	n/a	chr4:53411796-53411817 chr4:53411797-53411810 chr4:53411794-53411812
50	CTCF	chr4:53411659-53411662	LNCaP	prostate:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:53411703-53411753	HUVEC	blood vessel:	n/a
2	chr4:53411703-53411753	NT2-D1	testis:	n/a
3	chr4:53433409-53433459	Hela-S3	cervix:	n/a
4	chr4:53433409-53433459	ECC-1	luminal epithelium:	n/a
5	chr4:53433409-53433459	Jurkat	blood:	n/a
6	chr4:53433409-53433459	HUVEC	blood vessel:	n/a
7	chr4:53433409-53433459	NH-A	brain:	n/a
8	chr4:53411703-53411753	Jurkat	blood:	n/a
9	chr4:53411703-53411753	AG10803	skin:	n/a
10	chr4:53411703-53411753	HNPCEpiC	eye:	n/a
11	chr4:53411703-53411753	HEEpiC	esophagus:	n/a
12	chr4:53433409-53433459	HCF	heart:	n/a
13	chr4:53433409-53433459	GM19239	blood:	n/a
14	chr4:53433409-53433459	ProgFib	skin:	n/a
15	chr4:53411703-53411753	U87	brain:	n/a
16	chr4:53411703-53411753	HRPEpiC	eye:	n/a
17	chr4:53433409-53433459	AG09309	skin:	n/a
18	chr4:53433409-53433459	MCF-7	breast:	n/a
19	chr4:53411703-53411753	GM19239	blood:	n/a
20	chr4:53433409-53433459	HNPCEpiC	eye:	n/a
21	chr4:53411703-53411753	HMEC	breast:	n/a
22	chr4:53411703-53411753	HCM	heart:	n/a
23	chr4:53411703-53411753	PFSK-1	brain:	n/a
24	chr4:53411703-53411753	HCPEpiC	choroid plexus:	n/a
25	chr4:53433409-53433459	AG10803	skin:	n/a
26	chr4:53433409-53433459	PrEC	prostate:	n/a
27	chr4:53433409-53433459	NHDF-neo	bronchial:	n/a
28	chr4:53433409-53433459	AG04449	skin:	fetal
29	chr4:53411703-53411753	IMR90	lung:	fetal
30	chr4:53411703-53411753	MCF-7	breast:	n/a
31	chr4:53433409-53433459	Hepatocyte	liver:	n/a
32	chr4:53411703-53411753	AG04450	lung:	fetal
33	chr4:53411703-53411753	HPAEpiC	pulmonary alveolar:	n/a
34	chr4:53433409-53433459	GM12878	blood:	n/a
35	chr4:53411703-53411753	AG04449	skin:	fetal
36	chr4:53411703-53411753	SK-N-SH_RA	brain:	n/a
37	chr4:53433409-53433459	HL-60	blood:	n/a
38	chr4:53411703-53411753	ECC-1	luminal epithelium:	n/a
39	chr4:53433409-53433459	BJ	skin:	n/a
40	chr4:53411703-53411753	HAEpiC	amniotic membrane:	n/a
41	chr4:53433409-53433459	K562	blood:	n/a
42	chr4:53433409-53433459	HMEC	breast:	n/a
43	chr4:53411703-53411753	BJ	skin:	n/a
44	chr4:53433409-53433459	HepG2	liver:	n/a
45	chr4:53433409-53433459	PFSK-1	brain:	n/a
46	chr4:53411703-53411753	GM06990	blood:	n/a
47	chr4:53433409-53433459	GM12892	blood:	n/a
48	chr4:53433409-53433459	SK-N-SH_RA	brain:	n/a
49	chr4:53433409-53433459	U87	brain:	n/a
50	chr4:53433409-53433459	AoSMC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:53411690..53412321-chr4:53531251..53531991,2	MCF-7	breast:
2	chr4:53411392..53412371-chr4:53849508..53850419,4	MCF-7	breast:
3	chr4:53435485..53437104-chr4:53439490..53441965,2	K562	blood:
4	chr4:53430440..53432417-chr4:53577534..53579094,2	MCF-7	breast:
5	chr4:53411298..53412068-chr4:53849507..53850396,5	K562	blood:
6	chr17:2878558..2879392-chr4:53434507..53435224,2	MCF-7	breast:
7	chr4:53416997..53419282-chr4:53420354..53422590,2	K562	blood:
8	chr4:53411345..53412275-chr4:53848642..53849410,3	MCF-7	breast:
9	chr4:53414793..53417097-chr4:53846819..53849228,3	MCF-7	breast:
10	chr4:53411566..53412277-chr4:53531544..53532289,2	MCF-7	breast:
11	chr4:53396647..53398236-chr4:53435310..53437098,2	K562	blood:
12	chr4:53424700..53426749-chr4:53432925..53434502,2	MCF-7	breast:
13	chr4:53415337..53418016-chr4:53578498..53580053,2	MCF-7	breast:
14	chr4:53241976..53242647-chr4:53411318..53412257,2	MCF-7	breast:
15	chr4:53396647..53398236-chr4:53435310..53437098,2	K562	blood:
16	chr4:53416997..53419282-chr4:53420354..53422590,2	K562	blood:
17	chr4:53412265..53413383-chr4:53849416..53850413,3	K562	blood:
18	chr4:53424700..53426749-chr4:53432925..53434502,2	MCF-7	breast:
19	chr4:53411349..53412285-chr4:53848309..53849353,5	MCF-7	breast:
20	chr4:53394568..53396767-chr4:53400837..53403254,2	K562	blood:
21	chr4:53338249..53340211-chr4:53343621..53345963,2	K562	blood:
22	chr4:53394568..53396767-chr4:53400837..53403254,2	K562	blood:
23	chr4:53338249..53340211-chr4:53343621..53345963,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-USP46-2	chr4:53423008-53423127	l_2644_chr4:53422039-53423108_testes
2	lnc-USP46-2	chr4:53422040-53422655	l_2644_chr4:53422039-53423108_testes

Variant related genes	Relation type
ENSG00000239068	TF binding region
RNU6-1252P	TF binding region
ENSG00000239068	CpG island
RNU6-1252P	CpG island
ENSG00000264585	chromatin interactions
ENSG00000226950	chromatin interactions
ENSG00000212588	chromatin interactions

Extended variants
information (count: 3080 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:3080 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs368979116	chr4:53343210-53343211	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs556527184	chr4:53343218-53343219	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs138432355	chr4:53343251-53343252	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs537577245	chr4:53343260-53343261	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs554114813	chr4:53343274-53343275	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs191998291	chr4:53343312-53343313	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs540095236	chr4:53343314-53343315	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs35861844	chr4:53343337-53343338	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs560017650	chr4:53343415-53343416	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs149280911	chr4:53343424-53343425	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs530497954	chr4:53343455-53343456	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs545967139	chr4:53343497-53343498	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs562573608	chr4:53343538-53343539	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs144504946	chr4:53343553-53343554	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs548724926	chr4:53343554-53343555	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs184595704	chr4:53343600-53343601	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs527697098	chr4:53343645-53343646	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs548064801	chr4:53343663-53343664	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs115574921	chr4:53343669-53343670	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs539786127	chr4:53343674-53343675	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs187785162	chr4:53343685-53343686	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs192612835	chr4:53343698-53343699	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs555026469	chr4:53343706-53343707	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs112473961	chr4:53343719-53343720	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs376433973	chr4:53343731-53343732	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs184295081	chr4:53343749-53343750	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs113990684	chr4:53343750-53343751	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs566038260	chr4:53343843-53343844	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs13127085	chr4:53343848-53343849	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs577049175	chr4:53343864-53343865	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs181273410	chr4:53343888-53343889	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs562677824	chr4:53343900-53343901	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs184685540	chr4:53343913-53343914	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs188575410	chr4:53343920-53343921	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs542305236	chr4:53343921-53343922	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs562168845	chr4:53343925-53343926	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs527836222	chr4:53343945-53343946	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs200164262	chr4:53343947-53343948	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs181405878	chr4:53344010-53344011	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs566236256	chr4:53344049-53344050	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs185941247	chr4:53344060-53344061	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs189236907	chr4:53344061-53344062	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs545142497	chr4:53344073-53344074	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs369984477	chr4:53344086-53344087	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs570190978	chr4:53344094-53344095	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs563791793	chr4:53344101-53344102	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs142150407	chr4:53344108-53344109	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs73149098	chr4:53344124-53344125	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs533672578	chr4:53344138-53344139	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs553327505	chr4:53344142-53344143	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:97)

Disease	PMID	Source
Gastrointestinal stromal cancer	16982739	CNVD
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
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	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
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Cancer	22183965	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	16272173	CNVD
Glioblastoma multiforme	19435819	CNVD
Multiple myeloma	16616336	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
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
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian neoplasms	16753589	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Glioblastoma multiforme	21569311	CNVD
Glioblastoma	17504929	CNVD
Glioblastoma	16823502	CNVD
Melanoma	16908931	CNVD
Glioblastoma	20031968	CNVD
Medulloblastoma	19270706	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Olfactory neuroblastoma	18408657	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Rhabdomyosarcoma	16790082	CNVD
Gastrointestinal stromal cancer	17438095	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	19208797	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD

Chromatin state (count:295 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:53343200-53344200	Enhancers	Cortex derived primary cultured neurospheres	brain
2	chr4:53345000-53345400	Enhancers	Stomach Smooth Muscle	stomach
3	chr4:53349400-53350200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr4:53350200-53355600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr4:53352600-53353000	Enhancers	Left Ventricle	heart
6	chr4:53352600-53353200	Enhancers	Ovary	ovary
7	chr4:53355200-53356000	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr4:53355400-53356000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr4:53355400-53356000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
10	chr4:53355600-53356000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr4:53356000-53361000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr4:53364800-53365000	Enhancers	Pancreas	Pancrea
13	chr4:53373200-53374000	Enhancers	Aorta	Aorta
14	chr4:53373200-53374000	Enhancers	Right Ventricle	heart
15	chr4:53373200-53374400	Enhancers	Left Ventricle	heart
16	chr4:53373200-53374800	Enhancers	Cortex derived primary cultured neurospheres	brain
17	chr4:53373400-53374000	Enhancers	Right Atrium	heart
18	chr4:53373400-53374400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr4:53373400-53374400	Enhancers	Ovary	ovary
20	chr4:53373600-53374600	Enhancers	Rectal Smooth Muscle	rectum
21	chr4:53373600-53374800	Enhancers	Colon Smooth Muscle	Colon
22	chr4:53374000-53378000	Weak transcription	Aorta	Aorta
23	chr4:53374000-53378000	Weak transcription	Right Atrium	heart
24	chr4:53374000-53388200	Weak transcription	Right Ventricle	heart
25	chr4:53374400-53375200	Weak transcription	Left Ventricle	heart
26	chr4:53374800-53378200	Weak transcription	Colon Smooth Muscle	Colon
27	chr4:53375400-53375600	Enhancers	Left Ventricle	heart
28	chr4:53375600-53377800	Weak transcription	Left Ventricle	heart
29	chr4:53376800-53379000	Enhancers	Fetal Heart	heart
30	chr4:53377400-53378800	Enhancers	Stomach Smooth Muscle	stomach
31	chr4:53377800-53378200	Enhancers	Left Ventricle	heart
32	chr4:53378000-53378200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
33	chr4:53378000-53378200	Enhancers	Right Atrium	heart
34	chr4:53378000-53378800	Enhancers	Aorta	Aorta
35	chr4:53378200-53378800	Enhancers	Colon Smooth Muscle	Colon
36	chr4:53378200-53389200	Weak transcription	Left Ventricle	heart
37	chr4:53378800-53388800	Weak transcription	Aorta	Aorta
38	chr4:53382800-53383000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr4:53382800-53383000	Enhancers	Pancreas	Pancrea
40	chr4:53383000-53385800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr4:53383000-53386800	Weak transcription	Pancreas	Pancrea
42	chr4:53385400-53387000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr4:53385800-53386000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr4:53386000-53386400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr4:53386400-53386800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr4:53388000-53388200	Enhancers	HepG2	liver
47	chr4:53388200-53388400	Flanking Active TSS	HepG2	liver
48	chr4:53388400-53388600	Active TSS	HepG2	liver
49	chr4:53402000-53402200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr4:53402000-53402400	Enhancers	Left Ventricle	heart

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