Variant report

Variant	nsv1013852
Chromosome Location	chr4:10287118-10320963
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	chr4:10306752-10306755	K562	blood:	n/a	n/a
2	BACH1	chr4:10291449-10291596	K562	blood:	n/a	n/a
3	BACH1	chr4:10296613-10296622	K562	blood:	n/a	n/a
4	CEBPB	chr4:10302967-10303233	K562	blood:	n/a	n/a
5	CEBPB	chr4:10304348-10304548	K562	blood:	n/a	n/a
6	CEBPB	chr4:10311017-10311187	HepG2	liver:	n/a	chr4:10311067-10311078
7	CEBPB	chr4:10310964-10311220	K562	blood:	n/a	chr4:10311067-10311078
8	CTCF	chr4:10314423-10314451	Lung_OC	lung:	n/a	n/a
9	CTCF	chr4:10318700-10318850	GM06990	blood:	n/a	n/a
10	CTCF	chr4:10299053-10299135	GM13976	blood:	n/a	n/a
11	CTCF	chr4:10303720-10303870	HMEC	breast:	n/a	n/a
12	CTCF	chr4:10319540-10319690	GM06990	blood:	n/a	n/a
13	CTCF	chr4:10320760-10320910	GM12872	blood:	n/a	n/a
14	E2F4	chr4:10295657-10295659	MCF10A-Er-Src	breast:	n/a	n/a
15	E2F4	chr4:10290559-10290673	MCF10A-Er-Src	breast:	n/a	n/a
16	ELF1	chr4:10291215-10291515	K562	blood:	n/a	chr4:10291316-10291329
17	EP300	chr4:10319177-10319351	K562	blood:	n/a	n/a
18	EP300	chr4:10306114-10306189	K562	blood:	n/a	n/a
19	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
20	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
21	FOS	chr4:10301304-10301511	MCF10A-Er-Src	breast:	n/a	n/a
22	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
23	FOS	chr4:10303929-10303965	MCF10A-Er-Src	breast:	n/a	n/a
24	FOS	chr4:10301280-10301608	MCF10A-Er-Src	breast:	n/a	n/a
25	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
26	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
27	FOS	chr4:10301338-10301508	MCF10A-Er-Src	breast:	n/a	n/a
28	IRF1	chr4:10297604-10297616	K562	blood:	n/a	n/a
29	IRF1	chr4:10303422-10303744	K562	blood:	n/a	n/a
30	IRF1	chr4:10303281-10303687	K562	blood:	n/a	n/a
31	JUN	chr4:10286454-10287177	K562	blood:	n/a	n/a
32	JUND	chr4:10291145-10291499	K562	blood:	n/a	n/a
33	MAFF	chr4:10318522-10318823	K562	blood:	n/a	n/a
34	MAFF	chr4:10312332-10312440	K562	blood:	n/a	n/a
35	MAFF	chr4:10291139-10291471	K562	blood:	n/a	chr4:10291285-10291299
36	MAFF	chr4:10320615-10320793	K562	blood:	n/a	chr4:10320647-10320661
37	MAFK	chr4:10291060-10291464	K562	blood:	n/a	chr4:10291287-10291303 chr4:10291282-10291302 chr4:10291291-10291302
38	MAFK	chr4:10310695-10310738	K562	blood:	n/a	n/a
39	MAFK	chr4:10291217-10291380	HepG2	liver:	n/a	chr4:10291287-10291303 chr4:10291282-10291302 chr4:10291291-10291302
40	MAFK	chr4:10320529-10320772	K562	blood:	n/a	chr4:10320646-10320662 chr4:10320649-10320665 chr4:10320651-10320660 chr4:10320647-10320661 chr4:10320644-10320664 chr4:10320648-10320657 chr4:10320648-10320658
41	MAFK	chr4:10320074-10320108	K562	blood:	n/a	n/a
42	MAFK	chr4:10318525-10318788	HepG2	liver:	n/a	chr4:10318668-10318683 chr4:10318672-10318683
43	MAFK	chr4:10318549-10318814	HepG2	liver:	n/a	chr4:10318668-10318683 chr4:10318672-10318683
44	MAX	chr4:10298319-10298686	H1-hESC	embryonic stem cell:	n/a	n/a
45	MAX	chr4:10298361-10298672	H1-hESC	embryonic stem cell:	n/a	n/a
46	MAX	chr4:10298314-10298656	H1-hESC	embryonic stem cell:	n/a	n/a
47	MAZ	chr4:10291398-10291512	K562	blood:	n/a	n/a
48	MYC	chr4:10307863-10307932	MCF10A-Er-Src	breast:	n/a	n/a
49	MYC	chr4:10320626-10320653	K562	blood:	n/a	n/a
50	MYC	chr4:10319132-10319311	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:10299145-10299195	PFSK-1	brain:	n/a
2	chr4:10299145-10299195	NB4	blood:	n/a
3	chr4:10299145-10299195	U87	brain:	n/a
4	chr4:10299145-10299195	HRCEpiC	kidney:	n/a
5	chr4:10299145-10299195	HCF	heart:	n/a
6	chr4:10299145-10299195	HEK293	kidney:	embryo
7	chr4:10299145-10299195	Hepatocyte	liver:	n/a
8	chr4:10299145-10299195	K562	blood:	n/a
9	chr4:10299145-10299195	SKMC	muscle:	n/a
10	chr4:10299145-10299195	NHDF-neo	bronchial:	n/a
11	chr4:10299145-10299195	HUVEC	blood vessel:	n/a
12	chr4:10299145-10299195	MCF10A-Er-Src	breast:	n/a
13	chr4:10299145-10299195	HCPEpiC	choroid plexus:	n/a
14	chr4:10299145-10299195	BE2_C	brain:	n/a
15	chr4:10299145-10299195	LNCaP	prostate:	n/a
16	chr4:10299145-10299195	CMK	blood:	n/a
17	chr4:10299145-10299195	AoSMC	blood vessel:	n/a
18	chr4:10299145-10299195	HAEpiC	amniotic membrane:	n/a
19	chr4:10299145-10299195	GM12878	blood:	n/a
20	chr4:10299145-10299195	SAEC	small airway:	n/a
21	chr4:10299145-10299195	HRE	kidney:	n/a
22	chr4:10299145-10299195	RPTEC	kidney:	n/a
23	chr4:10299145-10299195	HCT-116	colon:	n/a
24	chr4:10299145-10299195	HPAEpiC	pulmonary alveolar:	n/a
25	chr4:10299145-10299195	T-47D	breast:	n/a
26	chr4:10299145-10299195	SK-N-SH	brain:	n/a
27	chr4:10299145-10299195	HEEpiC	esophagus:	n/a
28	chr4:10299145-10299195	AG09319	gingival:	n/a
29	chr4:10299145-10299195	PrEC	prostate:	n/a
30	chr4:10299145-10299195	ECC-1	luminal epithelium:	n/a
31	chr4:10299145-10299195	HCM	heart:	n/a
32	chr4:10299145-10299195	Jurkat	blood:	n/a
33	chr4:10299145-10299195	H1-hESC	embryonic stem cell:	embryo
34	chr4:10299145-10299195	NH-A	brain:	n/a
35	chr4:10299145-10299195	Caco-2	colon:	n/a
36	chr4:10299145-10299195	AG10803	skin:	n/a
37	chr4:10299145-10299195	BJ	skin:	n/a
38	chr4:10299145-10299195	AG04450	lung:	fetal
39	chr4:10299145-10299195	MCF-7	breast:	n/a
40	chr4:10299145-10299195	AG09309	skin:	n/a
41	chr4:10299145-10299195	Hela-S3	cervix:	n/a
42	chr4:10299145-10299195	ovcar-3	ovarian:	n/a
43	chr4:10299145-10299195	GM12891	blood:	n/a
44	chr4:10299145-10299195	HRPEpiC	eye:	n/a
45	chr4:10299145-10299195	AG04449	skin:	fetal
46	chr4:10299145-10299195	HMEC	breast:	n/a
47	chr4:10299145-10299195	SK-N-MC	brain:	n/a
48	chr4:10299145-10299195	SK-N-SH_RA	brain:	n/a
49	chr4:10299145-10299195	ProgFib	skin:	n/a
50	chr4:10299145-10299195	GM12892	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:10298581..10300458-chr4:10305111..10307586,2	K562	blood:
2	chr4:10312898..10315516-chr4:10318323..10320073,4	K562	blood:
3	chr4:10305228..10307997-chr4:10310331..10312718,2	K562	blood:
4	chr4:10306958..10308632-chr4:10319609..10321643,2	K562	blood:
5	chr4:10306958..10308632-chr4:10319609..10321643,2	K562	blood:
6	chr4:10116497..10118720-chr4:10304788..10307219,2	K562	blood:
7	chr4:10289644..10291282-chr4:10323806..10326517,2	K562	blood:
8	chr4:10293712..10297687-chr4:10307102..10309576,3	K562	blood:
9	chr4:10300976..10303713-chr4:10304138..10305960,3	K562	blood:
10	chr4:10303834..10305662-chr4:10370006..10372655,2	K562	blood:
11	chr4:10301025..10303713-chr4:10304138..10305960,2	K562	blood:
12	chr4:10120346..10122319-chr4:10312436..10314039,2	K562	blood:
13	chr4:10181898..10186356-chr4:10317430..10320755,4	K562	blood:
14	chr4:10301025..10303713-chr4:10304138..10305960,2	K562	blood:
15	chr4:10300976..10303713-chr4:10304138..10305960,3	K562	blood:
16	chr4:10182494..10184635-chr4:10284696..10287291,2	K562	blood:
17	chr4:10226621..10229156-chr4:10309809..10312332,2	K562	blood:
18	chr4:10305228..10307997-chr4:10310331..10312718,2	K562	blood:
19	chr4:10298581..10300458-chr4:10305111..10307586,2	K562	blood:
20	chr4:10283364..10286619-chr4:10288507..10291288,3	K562	blood:
21	chr4:10290044..10292857-chr4:10295207..10297834,2	K562	blood:
22	chr4:10278587..10280479-chr4:10297418..10299087,2	K562	blood:
23	chr4:10288926..10293598-chr4:10293770..10299284,5	K562	blood:
24	chr4:10119978..10123045-chr4:10320529..10323793,3	K562	blood:
25	chr4:10182494..10184107-chr4:10284696..10287149,2	K562	blood:
26	chr4:10312898..10315516-chr4:10318323..10320073,4	K562	blood:
27	chr4:10313155..10314762-chr4:10457693..10459658,2	K562	blood:
28	chr4:10320256..10323019-chr4:10334627..10337093,2	K562	blood:
29	chr4:10118483..10121328-chr4:10309961..10311571,2	K562	blood:
30	chr4:10119416..10121932-chr4:10294541..10296176,2	K562	blood:
31	chr4:10186571..10188279-chr4:10316070..10319056,2	K562	blood:
32	chr4:10118597..10121491-chr4:10308024..10311461,4	K562	blood:
33	chr4:10119318..10121113-chr4:10298083..10300540,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF518B-3	chr4:10286585-10287332	NONHSAT095493
2	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
ENSG00000251278	chromatin interactions
ENSG00000251338	chromatin interactions
ENSG00000178163	chromatin interactions
ENSG00000223086	chromatin interactions
ENSG00000071127	chromatin interactions

Extended variants
information (count: 2247 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:2247 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs143694636	chr4:10287131-10287132	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
2	rs550692467	chr4:10287146-10287147	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
3	rs17475334	chr4:10287170-10287171	Enhancers Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs565181641	chr4:10287175-10287176	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
5	rs148117294	chr4:10287193-10287194	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
6	rs546972456	chr4:10287226-10287227	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
7	rs34779422	chr4:10287228-10287229	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
8	rs11932349	chr4:10287251-10287252	Enhancers Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs529710262	chr4:10287253-10287254	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
10	rs10489068	chr4:10287268-10287269	Enhancers Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs567712737	chr4:10287279-10287280	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
12	rs12641365	chr4:10287305-10287306	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
13	rs550149432	chr4:10287314-10287315	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
14	rs77106098	chr4:10287319-10287320	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
15	rs539371338	chr4:10287324-10287325	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
16	rs554181070	chr4:10287337-10287338	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs572490010	chr4:10287378-10287379	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs536308935	chr4:10287405-10287406	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs73224405	chr4:10287415-10287416	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs188349905	chr4:10287438-10287439	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs112872904	chr4:10287445-10287446	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs150556356	chr4:10287451-10287452	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs576701847	chr4:10287459-10287460	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs535365823	chr4:10287472-10287473	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs553385220	chr4:10287500-10287501	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs139942273	chr4:10287508-10287509	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs558887235	chr4:10287516-10287517	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs529700519	chr4:10287521-10287522	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs547925051	chr4:10287526-10287527	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs376643328	chr4:10287535-10287536	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs563390061	chr4:10287540-10287541	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs62288124	chr4:10287550-10287551	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs11945358	chr4:10287559-10287560	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs571891721	chr4:10287563-10287564	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs59308796	chr4:10287570-10287571	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs146275373	chr4:10287572-10287573	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs116027100	chr4:10287594-10287595	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs566034056	chr4:10287602-10287603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs114498380	chr4:10287617-10287618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs557429990	chr4:10287645-10287646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs75060226	chr4:10287650-10287651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs59409126	chr4:10287673-10287674	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs17475461	chr4:10287677-10287678	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs546235874	chr4:10287699-10287700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs180866545	chr4:10287701-10287702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs566609463	chr4:10287705-10287706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs533726917	chr4:10287738-10287739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs185680166	chr4:10287766-10287767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs556419287	chr4:10287779-10287780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs540885037	chr4:10287782-10287783	Weak transcription	n/a	n/a	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:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:10282200-10287600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr4:10283000-10287200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr4:10283000-10287600	Enhancers	HMEC	breast
4	chr4:10283200-10287600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr4:10283200-10287600	Enhancers	NHEK	skin
6	chr4:10284800-10291200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr4:10286000-10287600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr4:10286000-10287600	Enhancers	K562	blood
9	chr4:10287200-10289200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr4:10287600-10289200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr4:10287600-10289400	Weak transcription	NHEK	skin
12	chr4:10287600-10289600	Weak transcription	HMEC	breast
13	chr4:10287600-10289600	Weak transcription	K562	blood
14	chr4:10287600-10289800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr4:10289200-10292400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr4:10289200-10293200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr4:10289400-10292800	Enhancers	NHEK	skin
18	chr4:10289600-10290000	Enhancers	K562	blood
19	chr4:10289600-10292800	Enhancers	HMEC	breast
20	chr4:10289800-10293200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr4:10290000-10291000	Weak transcription	K562	blood
22	chr4:10291000-10291800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr4:10291000-10292800	Enhancers	K562	blood
24	chr4:10291200-10291600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr4:10291600-10296800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr4:10292600-10292800	Enhancers	Cortex derived primary cultured neurospheres	brain
27	chr4:10292800-10297000	Weak transcription	HMEC	breast
28	chr4:10293200-10296800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr4:10293200-10298000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr4:10294200-10294800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr4:10294800-10297200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr4:10295200-10296400	Enhancers	Thymus	Thymus
33	chr4:10296600-10298600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr4:10296800-10297400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr4:10296800-10298400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr4:10297000-10297200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr4:10297000-10298000	Enhancers	Brain Substantia Nigra	brain
38	chr4:10297000-10299000	Enhancers	HMEC	breast
39	chr4:10297200-10298200	Enhancers	Brain Hippocampus Middle	brain
40	chr4:10297200-10298800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr4:10297200-10299600	Enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr4:10297200-10299800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr4:10297400-10298000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr4:10297400-10298200	Enhancers	Brain Anterior Caudate	brain
45	chr4:10297400-10300000	Enhancers	Cortex derived primary cultured neurospheres	brain
46	chr4:10297600-10298200	Enhancers	Brain Cingulate Gyrus	brain
47	chr4:10297600-10298200	Enhancers	Brain Inferior Temporal Lobe	brain
48	chr4:10297600-10298400	Enhancers	Fetal Brain Male	brain
49	chr4:10297800-10298000	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr4:10297800-10298600	Enhancers	Brain Angular Gyrus	brain

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