Variant report

Variant	nsv1010104
Chromosome Location	chr4:78520674-78553754
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	ATF2	chr4:78551030-78551511	GM12878	blood:	n/a	n/a
2	ATF2	chr4:78550906-78551569	GM12878	blood:	n/a	n/a
3	ATF3	chr4:78538436-78538714	K562	blood:	n/a	n/a
4	BACH1	chr4:78539784-78540196	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr4:78550905-78551525	GM12878	blood:	n/a	chr4:78551241-78551252
6	BATF	chr4:78550972-78551452	GM12878	blood:	n/a	chr4:78551241-78551252
7	BCL11A	chr4:78551047-78551453	GM12878	blood:	n/a	n/a
8	BHLHE40	chr4:78539876-78540051	K562	blood:	n/a	n/a
9	BHLHE40	chr4:78551096-78551411	GM12878	blood:	n/a	n/a
10	BHLHE40	chr4:78539858-78540151	GM12878	blood:	n/a	n/a
11	CEBPB	chr4:78538462-78538704	K562	blood:	n/a	chr4:78538568-78538579
12	CEBPB	chr4:78538356-78538709	ECC-1	luminal epithelium:	n/a	chr4:78538568-78538579
13	CEBPB	chr4:78530887-78531327	K562	blood:	n/a	chr4:78531015-78531026 chr4:78531211-78531224
14	CEBPB	chr4:78538327-78538696	MCF-7	breast:	n/a	chr4:78538568-78538579
15	CEBPB	chr4:78538433-78538630	K562	blood:	n/a	chr4:78538568-78538579
16	CEBPB	chr4:78538444-78538698	A549	lung:	n/a	chr4:78538568-78538579
17	CEBPB	chr4:78530924-78531307	A549	lung:	n/a	chr4:78531015-78531026 chr4:78531211-78531224
18	CEBPB	chr4:78538414-78538728	A549	lung:	n/a	chr4:78538568-78538579
19	CEBPB	chr4:78538391-78538749	K562	blood:	n/a	chr4:78538568-78538579
20	CEBPB	chr4:78538410-78538741	IMR90	lung:	n/a	chr4:78538568-78538579
21	CEBPB	chr4:78530966-78531229	H1-hESC	embryonic stem cell:	n/a	chr4:78531015-78531026 chr4:78531211-78531224
22	CEBPB	chr4:78538409-78538712	HepG2	liver:	n/a	chr4:78538568-78538579
23	CEBPB	chr4:78538340-78538729	A549	lung:	n/a	chr4:78538568-78538579
24	CEBPB	chr4:78530876-78531374	IMR90	lung:	n/a	chr4:78531015-78531026 chr4:78531211-78531224
25	CEBPB	chr4:78549677-78549804	IMR90	lung:	n/a	n/a
26	CEBPB	chr4:78538307-78538700	MCF-7	breast:	n/a	chr4:78538568-78538579
27	CEBPB	chr4:78538385-78538776	Hela-S3	cervix:	n/a	chr4:78538568-78538579
28	CEBPB	chr4:78530861-78531304	HepG2	liver:	n/a	chr4:78531015-78531026 chr4:78531211-78531224
29	CEBPB	chr4:78553733-78554021	HepG2	liver:	n/a	chr4:78553875-78553886
30	CEBPB	chr4:78538469-78538685	H1-hESC	embryonic stem cell:	n/a	chr4:78538568-78538579
31	CHD1	chr4:78540074-78540193	GM12878	blood:	n/a	n/a
32	CHD2	chr4:78539829-78540078	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD2	chr4:78551319-78551335	GM12878	blood:	n/a	n/a
34	CTCF	chr4:78522160-78522310	AG09319	gingival:	n/a	n/a
35	CTCF	chr4:78521770-78521802	Pancreas_OC	pancreas:	n/a	n/a
36	CTCF	chr4:78539960-78540110	AG04450	lung:	n/a	chr4:78539986-78539995 chr4:78539981-78539997 chr4:78539980-78539998 chr4:78539982-78539995 chr4:78539975-78539996
37	CTCF	chr4:78522140-78522290	BJ	skin:	n/a	n/a
38	CTCF	chr4:78521680-78521830	GM12867	blood:	n/a	n/a
39	CTCF	chr4:78539794-78540127	K562	blood:	n/a	chr4:78539986-78539995 chr4:78539981-78539997 chr4:78539980-78539998 chr4:78539982-78539995 chr4:78539975-78539996
40	CTCF	chr4:78522260-78522410	A549	lung:	n/a	n/a
41	CTCF	chr4:78520433-78521218	SK-N-SH	brain:	n/a	chr4:78520742-78520751
42	CTCF	chr4:78522140-78522290	Hela-S3	cervix:	n/a	n/a
43	CTCF	chr4:78539874-78540128	MCF-7	breast:	n/a	chr4:78539986-78539995 chr4:78539981-78539997 chr4:78539980-78539998 chr4:78539982-78539995 chr4:78539975-78539996
44	CTCF	chr4:78539920-78540070	GM12801	blood:	n/a	chr4:78539986-78539995 chr4:78539981-78539997 chr4:78539980-78539998 chr4:78539982-78539995 chr4:78539975-78539996
45	CTCF	chr4:78521260-78521410	HFF	foreskin:	n/a	n/a
46	CTCF	chr4:78522160-78522310	BE2_C	brain:	n/a	n/a
47	CTCF	chr4:78552817-78553055	K562	blood:	n/a	n/a
48	CTCF	chr4:78539687-78540292	MCF-7	breast:	n/a	chr4:78539986-78539995 chr4:78539981-78539997 chr4:78539980-78539998 chr4:78539982-78539995 chr4:78539975-78539996
49	CTCF	chr4:78539920-78540070	HPF	lung:	n/a	chr4:78539986-78539995 chr4:78539981-78539997 chr4:78539980-78539998 chr4:78539982-78539995 chr4:78539975-78539996
50	CTCF	chr4:78520594-78520907	HepG2	liver:	n/a	chr4:78520742-78520751

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:78532698-78532748	CMK	blood:	n/a
2	chr4:78529898-78529948	AG04450	lung:	fetal
3	chr4:78532698-78532748	BJ	skin:	n/a
4	chr4:78532698-78532748	AG10803	skin:	n/a
5	chr4:78529898-78529948	NHBE	bronchial:	n/a
6	chr4:78529898-78529948	HEEpiC	esophagus:	n/a
7	chr4:78532698-78532748	HL-60	blood:	n/a
8	chr4:78529898-78529948	ECC-1	luminal epithelium:	n/a
9	chr4:78532698-78532748	MCF10A-Er-Src	breast:	n/a
10	chr4:78532698-78532748	HepG2	liver:	n/a
11	chr4:78529898-78529948	HRCEpiC	kidney:	n/a
12	chr4:78532698-78532748	Caco-2	colon:	n/a
13	chr4:78529898-78529948	AG10803	skin:	n/a
14	chr4:78529898-78529948	Jurkat	blood:	n/a
15	chr4:78529898-78529948	Hela-S3	cervix:	n/a
16	chr4:78532698-78532748	K562	blood:	n/a
17	chr4:78532698-78532748	AoSMC	blood vessel:	n/a
18	chr4:78532698-78532748	SK-N-SH	brain:	n/a
19	chr4:78529898-78529948	SK-N-SH_RA	brain:	n/a
20	chr4:78529898-78529948	GM12891	blood:	n/a
21	chr4:78529898-78529948	ovcar-3	ovarian:	n/a
22	chr4:78532698-78532748	HCPEpiC	choroid plexus:	n/a
23	chr4:78529898-78529948	HIPEpiC	eye:	n/a
24	chr4:78532698-78532748	SK-N-MC	brain:	n/a
25	chr4:78532698-78532748	AG09309	skin:	n/a
26	chr4:78529898-78529948	AoSMC	blood vessel:	n/a
27	chr4:78532698-78532748	Hepatocyte	liver:	n/a
28	chr4:78529898-78529948	NH-A	brain:	n/a
29	chr4:78532698-78532748	H1-hESC	embryonic stem cell:	embryo
30	chr4:78532698-78532748	PFSK-1	brain:	n/a
31	chr4:78529898-78529948	GM06990	blood:	n/a
32	chr4:78532698-78532748	SKMC	muscle:	n/a
33	chr4:78529898-78529948	RPTEC	kidney:	n/a
34	chr4:78529898-78529948	SK-N-MC	brain:	n/a
35	chr4:78529898-78529948	GM12878	blood:	n/a
36	chr4:78532698-78532748	U87	brain:	n/a
37	chr4:78532698-78532748	AG09319	gingival:	n/a
38	chr4:78532698-78532748	MCF-7	breast:	n/a
39	chr4:78529898-78529948	IMR90	lung:	fetal
40	chr4:78529898-78529948	HPAEpiC	pulmonary alveolar:	n/a
41	chr4:78529898-78529948	BJ	skin:	n/a
42	chr4:78532698-78532748	AG04450	lung:	fetal
43	chr4:78529898-78529948	HRPEpiC	eye:	n/a
44	chr4:78529898-78529948	PFSK-1	brain:	n/a
45	chr4:78529898-78529948	NHDF-neo	bronchial:	n/a
46	chr4:78529898-78529948	SKMC	muscle:	n/a
47	chr4:78532698-78532748	HEEpiC	esophagus:	n/a
48	chr4:78529898-78529948	HepG2	liver:	n/a
49	chr4:78532698-78532748	PrEC	prostate:	n/a
50	chr4:78529898-78529948	GM12892	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:78306302..78306941-chr4:78521930..78522730,3	MCF-7	breast:
2	chr4:78521817..78522700-chr4:78619204..78620028,2	MCF-7	breast:
3	chr4:78385938..78387056-chr4:78521715..78522661,6	MCF-7	breast:
4	chr4:78306259..78307081-chr4:78539517..78540020,2	K562	blood:
5	chr4:78540911..78543447-chr4:78545553..78547631,2	MCF-7	breast:
6	chr4:78521675..78522522-chr5:128453764..128454552,2	K562	blood:
7	chr4:78530875..78532515-chr4:78534945..78537935,2	K562	blood:
8	chr4:78386426..78387105-chr4:78521722..78522272,2	MCF-7	breast:
9	chr4:78354236..78354764-chr4:78521810..78522404,2	MCF-7	breast:
10	chr4:78386033..78387001-chr4:78522641..78523414,2	MCF-7	breast:
11	chr4:78386143..78387109-chr4:78539081..78540489,9	MCF-7	breast:
12	chr4:78528761..78530717-chr4:78532586..78534961,2	MCF-7	breast:
13	chr4:78521938..78522727-chr4:78539308..78540406,4	MCF-7	breast:
14	chr4:78386155..78387048-chr4:78520300..78520908,2	MCF-7	breast:
15	chr4:78539680..78541728-chr4:78543487..78545525,2	MCF-7	breast:
16	chr4:78528761..78530717-chr4:78532586..78534961,2	MCF-7	breast:
17	chr4:78394741..78395310-chr4:78522044..78522649,2	MCF-7	breast:
18	chr4:78306282..78306818-chr4:78539506..78540132,2	MCF-7	breast:
19	chr4:78522249..78524588-chr4:78525171..78527688,2	MCF-7	breast:
20	chr4:78532722..78535241-chr4:78538489..78541830,3	MCF-7	breast:
21	chr4:78521938..78522727-chr4:78539308..78540406,4	MCF-7	breast:
22	chr4:78532722..78535241-chr4:78538489..78541830,3	MCF-7	breast:
23	chr4:78539680..78541728-chr4:78543487..78545525,2	MCF-7	breast:
24	chr4:78540911..78543447-chr4:78545553..78547631,2	MCF-7	breast:
25	chr4:78386180..78387155-chr4:78519855..78521281,5	MCF-7	breast:
26	chr4:78530875..78532515-chr4:78534945..78537935,2	K562	blood:
27	chr4:78354631..78355201-chr4:78520510..78521240,2	MCF-7	breast:
28	chr4:78394433..78394946-chr4:78521807..78522340,2	MCF-7	breast:
29	chr4:78539512..78540036-chr4:78619176..78619985,2	MCF-7	breast:
30	chr4:78538801..78540562-chr4:78562420..78564607,2	MCF-7	breast:
31	chr4:78515499..78517664-chr4:78519423..78521638,2	MCF-7	breast:
32	chr4:78552964..78554952-chr4:78555723..78558165,2	MCF-7	breast:
33	chr4:78394658..78395254-chr4:78520671..78521209,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CCNG2-3	chr4:78531768-78532076	NONHSAT097055
2	lnc-CCNG2-3	chr4:78526986-78527083	NONHSAT097055
3	lnc-CCNG2-3	chr4:78528857-78528989	NONHSAT097055

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	CXCL13	hsa-miR-26b-5p	chr4:78532460-78532483

Variant related genes	Relation type
CXCL13	TF binding region
CXCL13	CpG island
ENSG00000156234	chromatin interactions

Extended variants
information (count: 1220 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:1220 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2165722	chr4:78521203-78521204	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs563833455	chr4:78521218-78521219	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs113154626	chr4:78521248-78521249	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs529354992	chr4:78521364-78521365	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs549423460	chr4:78521369-78521370	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs191819592	chr4:78521417-78521418	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs534968920	chr4:78521428-78521429	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs143139048	chr4:78521473-78521474	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs171388	chr4:78521525-78521526	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs537686457	chr4:78521564-78521565	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs557249530	chr4:78521565-78521566	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs147489051	chr4:78521617-78521618	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs183432816	chr4:78521654-78521655	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs555397455	chr4:78521674-78521675	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs62304089	chr4:78521730-78521731	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs6829547	chr4:78521731-78521732	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs139835084	chr4:78521751-78521752	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs77387354	chr4:78521779-78521780	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs543638469	chr4:78521787-78521788	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs150785778	chr4:78521812-78521813	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs529057688	chr4:78521816-78521817	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs139221440	chr4:78521839-78521840	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs530417095	chr4:78521857-78521858	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs559844099	chr4:78521863-78521864	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs79815226	chr4:78521877-78521878	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs149929841	chr4:78521945-78521946	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs368691613	chr4:78521947-78521948	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs558726818	chr4:78522032-78522033	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs188882814	chr4:78522056-78522057	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs551219046	chr4:78522077-78522078	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs567781901	chr4:78522081-78522082	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs536817056	chr4:78522169-78522170	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs555215126	chr4:78522176-78522177	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs565436139	chr4:78522182-78522183	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs192044117	chr4:78522183-78522184	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs557316106	chr4:78522189-78522190	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs577185602	chr4:78522192-78522193	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs183393893	chr4:78522199-78522200	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs557174394	chr4:78522230-78522231	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs116032776	chr4:78522263-78522264	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs80316685	chr4:78522352-78522353	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs146493759	chr4:78522358-78522359	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs373655345	chr4:78522405-78522406	Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs139856208	chr4:78522449-78522450	Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs186612421	chr4:78522515-78522516	Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs576425429	chr4:78522573-78522574	Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs7678830	chr4:78522686-78522687	Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs565291910	chr4:78522750-78522751	Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs538288469	chr4:78522778-78522779	Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs530903981	chr4:78522842-78522843	Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:75)

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
Glioblastoma multiforme	21922591	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
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
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
primary effusion lymphomas	17116491	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:160 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:78521200-78523600	Enhancers	Liver	Liver
2	chr4:78521400-78522400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr4:78521600-78522400	Enhancers	Primary T helper cells PMA-I stimulated	--
4	chr4:78522200-78523600	Enhancers	HMEC	breast
5	chr4:78522400-78523000	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr4:78522400-78523400	Enhancers	Breast Myoepithelial Primary Cells	Breast
7	chr4:78522400-78523800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr4:78522600-78523600	Enhancers	NHEK	skin
9	chr4:78522600-78523800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr4:78522800-78523600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr4:78523600-78526200	Weak transcription	Liver	Liver
12	chr4:78523800-78524400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr4:78524400-78524600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr4:78526000-78526200	Enhancers	Brain Germinal Matrix	brain
15	chr4:78526200-78526800	Enhancers	Liver	Liver
16	chr4:78526400-78527200	Enhancers	HepG2	liver
17	chr4:78526400-78527600	Weak transcription	Brain Germinal Matrix	brain
18	chr4:78527600-78527800	Enhancers	Fetal Lung	lung
19	chr4:78527600-78528400	Enhancers	Brain Germinal Matrix	brain
20	chr4:78528000-78530800	Weak transcription	Fetal Lung	lung
21	chr4:78529600-78540000	Weak transcription	Right Atrium	heart
22	chr4:78530800-78532000	Enhancers	Fetal Lung	lung
23	chr4:78532000-78544000	Weak transcription	Fetal Lung	lung
24	chr4:78534200-78534400	Enhancers	Adipose Nuclei	Adipose
25	chr4:78534400-78534600	Bivalent/Poised TSS	Osteobl	bone
26	chr4:78534400-78534800	Bivalent/Poised TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr4:78534400-78534800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr4:78534400-78534800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr4:78534400-78535000	Flanking Active TSS	Adipose Nuclei	Adipose
30	chr4:78534600-78534800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr4:78534600-78534800	Active TSS	Osteobl	bone
32	chr4:78534600-78535200	Enhancers	Skeletal Muscle Male	skeletal muscle
33	chr4:78534800-78535000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr4:78534800-78535000	Flanking Active TSS	Osteobl	bone
35	chr4:78534800-78535200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr4:78534800-78535200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr4:78535000-78535200	Enhancers	Adipose Nuclei	Adipose
38	chr4:78535000-78535200	Enhancers	Left Ventricle	heart
39	chr4:78535000-78535200	Enhancers	Osteobl	bone
40	chr4:78535200-78539600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr4:78535200-78539800	Weak transcription	Left Ventricle	heart
42	chr4:78535200-78539800	Weak transcription	Skeletal Muscle Male	skeletal muscle
43	chr4:78536400-78536800	Active TSS	GM12878-XiMat	blood
44	chr4:78538400-78538600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr4:78538400-78538600	Enhancers	HMEC	breast
46	chr4:78538400-78540200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr4:78538600-78539600	Weak transcription	HMEC	breast
48	chr4:78539600-78540000	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr4:78539600-78540000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr4:78539600-78540000	Enhancers	Brain Hippocampus Middle	brain

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