Variant report

Variant	nsv963589
Chromosome Location	chr4:10288617-10325163
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	BACH1	chr4:10291449-10291596	K562	blood:	n/a	n/a
2	BACH1	chr4:10296613-10296622	K562	blood:	n/a	n/a
3	BACH1	chr4:10306752-10306755	K562	blood:	n/a	n/a
4	CCNT2	chr4:10323672-10323734	K562	blood:	n/a	n/a
5	CEBPB	chr4:10311017-10311187	HepG2	liver:	n/a	chr4:10311067-10311078
6	CEBPB	chr4:10304348-10304548	K562	blood:	n/a	n/a
7	CEBPB	chr4:10302967-10303233	K562	blood:	n/a	n/a
8	CEBPB	chr4:10310964-10311220	K562	blood:	n/a	chr4:10311067-10311078
9	CTCF	chr4:10323640-10323790	WERI-Rb-1	eye:	n/a	n/a
10	CTCF	chr4:10323677-10323783	NHEK	skin:	n/a	n/a
11	CTCF	chr4:10314423-10314451	Lung_OC	lung:	n/a	n/a
12	CTCF	chr4:10321860-10322010	Caco-2	colon:	n/a	chr4:10321896-10321917 chr4:10321901-10321919
13	CTCF	chr4:10299053-10299135	GM13976	blood:	n/a	n/a
14	CTCF	chr4:10321791-10322026	HepG2	liver:	n/a	chr4:10321896-10321917 chr4:10321901-10321919
15	CTCF	chr4:10318700-10318850	GM06990	blood:	n/a	n/a
16	CTCF	chr4:10320760-10320910	GM12872	blood:	n/a	n/a
17	CTCF	chr4:10321860-10322010	HepG2	liver:	n/a	chr4:10321896-10321917 chr4:10321901-10321919
18	CTCF	chr4:10323660-10323810	WERI-Rb-1	eye:	n/a	n/a
19	CTCF	chr4:10321780-10321930	Caco-2	colon:	n/a	chr4:10321896-10321917 chr4:10321901-10321919
20	CTCF	chr4:10321840-10321990	GM12872	blood:	n/a	chr4:10321896-10321917 chr4:10321901-10321919
21	CTCF	chr4:10319540-10319690	GM06990	blood:	n/a	n/a
22	CTCF	chr4:10321840-10321990	HepG2	liver:	n/a	chr4:10321896-10321917 chr4:10321901-10321919
23	CTCF	chr4:10303720-10303870	HMEC	breast:	n/a	n/a
24	CTCF	chr4:10323611-10323811	K562	blood:	n/a	n/a
25	CTCF	chr4:10321837-10322004	HepG2	liver:	n/a	chr4:10321896-10321917 chr4:10321901-10321919
26	E2F4	chr4:10295657-10295659	MCF10A-Er-Src	breast:	n/a	n/a
27	E2F4	chr4:10290559-10290673	MCF10A-Er-Src	breast:	n/a	n/a
28	ELF1	chr4:10291215-10291515	K562	blood:	n/a	chr4:10291316-10291329
29	EP300	chr4:10319177-10319351	K562	blood:	n/a	n/a
30	EP300	chr4:10323706-10323891	K562	blood:	n/a	n/a
31	EP300	chr4:10321951-10322148	HepG2	liver:	n/a	n/a
32	EP300	chr4:10306114-10306189	K562	blood:	n/a	n/a
33	FOS	chr4:10290533-10290862	MCF10A-Er-Src	breast:	n/a	chr4:10290705-10290715 chr4:10290706-10290714 chr4:10290705-10290715 chr4:10290706-10290713 chr4:10290705-10290715 chr4:10290705-10290715 chr4:10290706-10290714
34	FOS	chr4:10290503-10291242	MCF10A-Er-Src	breast:	n/a	chr4:10290705-10290715 chr4:10290706-10290714 chr4:10290705-10290715 chr4:10290706-10290713 chr4:10290705-10290715 chr4:10290705-10290715 chr4:10290706-10290714
35	FOS	chr4:10301338-10301508	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr4:10301280-10301608	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr4:10290551-10290812	MCF10A-Er-Src	breast:	n/a	chr4:10290705-10290715 chr4:10290706-10290714 chr4:10290705-10290715 chr4:10290706-10290713 chr4:10290705-10290715 chr4:10290705-10290715 chr4:10290706-10290714
38	FOS	chr4:10303929-10303965	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr4:10290533-10290891	MCF10A-Er-Src	breast:	n/a	chr4:10290705-10290715 chr4:10290706-10290714 chr4:10290705-10290715 chr4:10290706-10290713 chr4:10290705-10290715 chr4:10290705-10290715 chr4:10290706-10290714
40	FOS	chr4:10301304-10301511	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr4:10290460-10290959	HUVEC	blood vessel:	n/a	chr4:10290705-10290715 chr4:10290706-10290714 chr4:10290705-10290715 chr4:10290706-10290713 chr4:10290705-10290715 chr4:10290705-10290715 chr4:10290706-10290714
42	HNF4A	chr4:10321773-10322156	HepG2	liver:	n/a	chr4:10321962-10321974 chr4:10321961-10321975 chr4:10321960-10321975 chr4:10321962-10321975 chr4:10321959-10321977 chr4:10321962-10321974 chr4:10321962-10321974 chr4:10321961-10321975 chr4:10321962-10321974 chr4:10321960-10321975 chr4:10321961-10321974 chr4:10321965-10321977 chr4:10321960-10321975
43	HNF4A	chr4:10321766-10322131	HepG2	liver:	n/a	chr4:10321962-10321974 chr4:10321961-10321975 chr4:10321960-10321975 chr4:10321962-10321975 chr4:10321959-10321977 chr4:10321962-10321974 chr4:10321962-10321974 chr4:10321961-10321975 chr4:10321962-10321974 chr4:10321960-10321975 chr4:10321961-10321974 chr4:10321965-10321977 chr4:10321960-10321975
44	HNF4G	chr4:10321742-10322147	HepG2	liver:	n/a	chr4:10321962-10321974 chr4:10321961-10321975 chr4:10321961-10321976 chr4:10321960-10321975 chr4:10321962-10321975 chr4:10321959-10321977 chr4:10321962-10321974 chr4:10321962-10321974 chr4:10321961-10321975 chr4:10321962-10321974 chr4:10321961-10321974 chr4:10321965-10321977 chr4:10321960-10321975
45	IRF1	chr4:10297604-10297616	K562	blood:	n/a	n/a
46	IRF1	chr4:10303281-10303687	K562	blood:	n/a	n/a
47	IRF1	chr4:10303422-10303744	K562	blood:	n/a	n/a
48	JUN	chr4:10321803-10322068	HepG2	liver:	n/a	chr4:10321931-10321944
49	JUND	chr4:10321779-10322118	HepG2	liver:	n/a	n/a
50	JUND	chr4:10291145-10291499	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:10299145-10299195	Caco-2	colon:	n/a
2	chr4:10299145-10299195	T-47D	breast:	n/a
3	chr4:10299145-10299195	HPAEpiC	pulmonary alveolar:	n/a
4	chr4:10299145-10299195	HUVEC	blood vessel:	n/a
5	chr4:10299145-10299195	IMR90	lung:	fetal
6	chr4:10299145-10299195	BJ	skin:	n/a
7	chr4:10299145-10299195	AG09309	skin:	n/a
8	chr4:10299145-10299195	K562	blood:	n/a
9	chr4:10299145-10299195	SK-N-SH	brain:	n/a
10	chr4:10299145-10299195	BE2_C	brain:	n/a
11	chr4:10299145-10299195	NHDF-neo	bronchial:	n/a
12	chr4:10299145-10299195	HRCEpiC	kidney:	n/a
13	chr4:10299145-10299195	GM12891	blood:	n/a
14	chr4:10299145-10299195	HRE	kidney:	n/a
15	chr4:10299145-10299195	PANC-1	pancreas:	n/a
16	chr4:10299145-10299195	GM06990	blood:	n/a
17	chr4:10299145-10299195	ECC-1	luminal epithelium:	n/a
18	chr4:10299145-10299195	MCF-7	breast:	n/a
19	chr4:10299145-10299195	GM12878	blood:	n/a
20	chr4:10299145-10299195	NB4	blood:	n/a
21	chr4:10299145-10299195	U87	brain:	n/a
22	chr4:10299145-10299195	LNCaP	prostate:	n/a
23	chr4:10299145-10299195	AG09319	gingival:	n/a
24	chr4:10299145-10299195	AG04449	skin:	fetal
25	chr4:10299145-10299195	HL-60	blood:	n/a
26	chr4:10299145-10299195	HNPCEpiC	eye:	n/a
27	chr4:10299145-10299195	HIPEpiC	eye:	n/a
28	chr4:10299145-10299195	HEEpiC	esophagus:	n/a
29	chr4:10299145-10299195	PrEC	prostate:	n/a
30	chr4:10299145-10299195	GM19239	blood:	n/a
31	chr4:10299145-10299195	NT2-D1	testis:	n/a
32	chr4:10299145-10299195	SK-N-MC	brain:	n/a
33	chr4:10299145-10299195	HCT-116	colon:	n/a
34	chr4:10299145-10299195	Hela-S3	cervix:	n/a
35	chr4:10299145-10299195	Jurkat	blood:	n/a
36	chr4:10299145-10299195	ProgFib	skin:	n/a
37	chr4:10299145-10299195	SK-N-SH_RA	brain:	n/a
38	chr4:10299145-10299195	NHBE	bronchial:	n/a
39	chr4:10299145-10299195	HMEC	breast:	n/a
40	chr4:10299145-10299195	GM12892	blood:	n/a
41	chr4:10299145-10299195	RPTEC	kidney:	n/a
42	chr4:10299145-10299195	H1-hESC	embryonic stem cell:	embryo
43	chr4:10299145-10299195	Hepatocyte	liver:	n/a
44	chr4:10299145-10299195	NH-A	brain:	n/a
45	chr4:10299145-10299195	SKMC	muscle:	n/a
46	chr4:10299145-10299195	AG10803	skin:	n/a
47	chr4:10299145-10299195	ovcar-3	ovarian:	n/a
48	chr4:10299145-10299195	PFSK-1	brain:	n/a
49	chr4:10299145-10299195	HAEpiC	amniotic membrane:	n/a
50	chr4:10299145-10299195	AoSMC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:10298581..10300458-chr4:10305111..10307586,2	K562	blood:
2	chr4:10289644..10291282-chr4:10323806..10326517,2	K562	blood:
3	chr4:10116497..10118720-chr4:10304788..10307219,2	K562	blood:
4	chr19:17416908..17417590-chr4:10322243..10323174,2	Hela-S3	cervix:
5	chr4:10322922..10325786-chr4:10326394..10328675,2	K562	blood:
6	chr4:10120346..10122319-chr4:10312436..10314039,2	K562	blood:
7	chr4:10300976..10303713-chr4:10304138..10305960,3	K562	blood:
8	chr4:10289644..10291282-chr4:10323806..10326517,2	K562	blood:
9	chr4:10312898..10315516-chr4:10318323..10320073,4	K562	blood:
10	chr4:10306958..10308632-chr4:10319609..10321643,2	K562	blood:
11	chr4:10321044..10322655-chr4:10326498..10328725,2	K562	blood:
12	chr4:10186571..10188279-chr4:10316070..10319056,2	K562	blood:
13	chr4:10305228..10307997-chr4:10310331..10312718,2	K562	blood:
14	chr4:10303834..10305662-chr4:10370006..10372655,2	K562	blood:
15	chr4:10119978..10123045-chr4:10320529..10323793,3	K562	blood:
16	chr4:10300976..10303713-chr4:10304138..10305960,3	K562	blood:
17	chr4:10293712..10297687-chr4:10307102..10309576,3	K562	blood:
18	chr4:10118483..10121328-chr4:10309961..10311571,2	K562	blood:
19	chr4:10119529..10122770-chr4:10324822..10328767,4	K562	blood:
20	chr4:10181898..10186356-chr4:10317430..10320755,4	K562	blood:
21	chr4:10119318..10121113-chr4:10298083..10300540,2	K562	blood:
22	chr4:10306958..10308632-chr4:10319609..10321643,2	K562	blood:
23	chr4:10226621..10229156-chr4:10309809..10312332,2	K562	blood:
24	chr4:10312898..10315516-chr4:10318323..10320073,4	K562	blood:
25	chr4:10320256..10323019-chr4:10334627..10337093,2	K562	blood:
26	chr4:10118597..10121491-chr4:10308024..10311461,4	K562	blood:
27	chr4:10305228..10307997-chr4:10310331..10312718,2	K562	blood:
28	chr4:10301025..10303713-chr4:10304138..10305960,2	K562	blood:
29	chr4:10290044..10292857-chr4:10295207..10297834,2	K562	blood:
30	chr4:10278587..10280479-chr4:10297418..10299087,2	K562	blood:
31	chr4:10313155..10314762-chr4:10457693..10459658,2	K562	blood:
32	chr4:10298581..10300458-chr4:10305111..10307586,2	K562	blood:
33	chr4:10288926..10293598-chr4:10293770..10299284,5	K562	blood:
34	chr4:10283364..10286619-chr4:10288507..10291288,3	K562	blood:
35	chr4:10119416..10121932-chr4:10294541..10296176,2	K562	blood:
36	chr4:10301025..10303713-chr4:10304138..10305960,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF518B-2	chr4:10293819-10294332	NONHSAT095494

Variant related genes	Relation type
ENSG00000251338	TF binding region
ENSG00000251278	TF binding region
ENSG00000250505	TF binding region
ENSG00000251338	CpG island
ENSG00000251278	CpG island
ENSG00000250505	CpG island
ENSG00000071127	chromatin interactions
ENSG00000251278	chromatin interactions
ENSG00000178163	chromatin interactions
ENSG00000223086	chromatin interactions
ENSG00000251338	chromatin interactions

Extended variants
information (count: 2437 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:2437 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs559861100	chr4:10288617-10288618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs574941302	chr4:10288618-10288619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs140303622	chr4:10288620-10288621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs563822210	chr4:10288626-10288627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs531145419	chr4:10288633-10288634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs187396135	chr4:10288634-10288635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs116316717	chr4:10288652-10288653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs192090444	chr4:10288696-10288697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs528534273	chr4:10288724-10288725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs546008931	chr4:10288727-10288728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs546787933	chr4:10288774-10288775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs568200507	chr4:10288810-10288811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs535288998	chr4:10288814-10288815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs550794380	chr4:10288831-10288832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs569155927	chr4:10288846-10288847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs184141733	chr4:10288851-10288852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs145074920	chr4:10288853-10288854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs557919807	chr4:10288868-10288869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs572891403	chr4:10288901-10288902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs186960372	chr4:10288923-10288924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs371513803	chr4:10288927-10288928	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs7670709	chr4:10288932-10288933	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs192424169	chr4:10288938-10288939	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs184549300	chr4:10288950-10288951	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs557562233	chr4:10288962-10288963	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs575507024	chr4:10288971-10288972	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs138637357	chr4:10288976-10288977	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs564102465	chr4:10288995-10288996	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs58129559	chr4:10288999-10289000	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs540670588	chr4:10289020-10289021	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs7685865	chr4:10289039-10289040	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs529424223	chr4:10289077-10289078	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs75383071	chr4:10289106-10289107	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs56412703	chr4:10289152-10289153	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs115035074	chr4:10289157-10289158	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs146264951	chr4:10289199-10289200	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs114084849	chr4:10289215-10289216	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs189028969	chr4:10289219-10289220	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs555381182	chr4:10289231-10289232	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs148064977	chr4:10289236-10289237	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs537968544	chr4:10289245-10289246	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs557239402	chr4:10289266-10289267	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs575443069	chr4:10289273-10289274	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs769091	chr4:10289280-10289281	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs558029675	chr4:10289301-10289302	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs573243544	chr4:10289305-10289306	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs141807313	chr4:10289313-10289314	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs562139307	chr4:10289360-10289361	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs529338816	chr4:10289381-10289382	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs544705556	chr4:10289382-10289383	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:54)

Disease	PMID	Source
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	22241247	CNVD
Autosomal-dominant microtia	18179897	CNVD
Glioma	17123091	CNVD
Colorectal cancer	20459617	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:182 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:10284800-10291200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr4:10287200-10289200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr4:10287600-10289200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr4:10287600-10289400	Weak transcription	NHEK	skin
5	chr4:10287600-10289600	Weak transcription	HMEC	breast
6	chr4:10287600-10289600	Weak transcription	K562	blood
7	chr4:10287600-10289800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr4:10289200-10292400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr4:10289200-10293200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr4:10289400-10292800	Enhancers	NHEK	skin
11	chr4:10289600-10290000	Enhancers	K562	blood
12	chr4:10289600-10292800	Enhancers	HMEC	breast
13	chr4:10289800-10293200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr4:10290000-10291000	Weak transcription	K562	blood
15	chr4:10291000-10291800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr4:10291000-10292800	Enhancers	K562	blood
17	chr4:10291200-10291600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr4:10291600-10296800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr4:10292600-10292800	Enhancers	Cortex derived primary cultured neurospheres	brain
20	chr4:10292800-10297000	Weak transcription	HMEC	breast
21	chr4:10293200-10296800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr4:10293200-10298000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr4:10294200-10294800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr4:10294800-10297200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr4:10295200-10296400	Enhancers	Thymus	Thymus
26	chr4:10296600-10298600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr4:10296800-10297400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr4:10296800-10298400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr4:10297000-10297200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr4:10297000-10298000	Enhancers	Brain Substantia Nigra	brain
31	chr4:10297000-10299000	Enhancers	HMEC	breast
32	chr4:10297200-10298200	Enhancers	Brain Hippocampus Middle	brain
33	chr4:10297200-10298800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr4:10297200-10299600	Enhancers	Breast Myoepithelial Primary Cells	Breast
35	chr4:10297200-10299800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr4:10297400-10298000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr4:10297400-10298200	Enhancers	Brain Anterior Caudate	brain
38	chr4:10297400-10300000	Enhancers	Cortex derived primary cultured neurospheres	brain
39	chr4:10297600-10298200	Enhancers	Brain Cingulate Gyrus	brain
40	chr4:10297600-10298200	Enhancers	Brain Inferior Temporal Lobe	brain
41	chr4:10297600-10298400	Enhancers	Fetal Brain Male	brain
42	chr4:10297800-10298000	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr4:10297800-10298600	Enhancers	Brain Angular Gyrus	brain
44	chr4:10298000-10298200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr4:10298000-10298400	Flanking Active TSS	Brain Substantia Nigra	brain
46	chr4:10298000-10298800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr4:10298000-10299000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr4:10298000-10299000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr4:10298000-10299000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr4:10298000-10299000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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