Variant report

Variant	nsv1010991
Chromosome Location	chr4:10398306-10410179
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	chr4:10405152-10405708	K562	blood:	n/a	n/a
2	BHLHE40	chr4:10405415-10405586	K562	blood:	n/a	n/a
3	CCNT2	chr4:10405344-10405663	K562	blood:	n/a	n/a
4	CEBPB	chr4:10405274-10405653	K562	blood:	n/a	n/a
5	CEBPB	chr4:10408033-10408219	K562	blood:	n/a	chr4:10408128-10408141
6	CTCF	chr4:10405460-10405610	GM12872	blood:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
7	CTCF	chr4:10405240-10405390	HMEC	breast:	n/a	n/a
8	CTCF	chr4:10405416-10405678	SK-N-SH_RA	brain:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
9	CTCF	chr4:10405500-10405650	NHDF-neo	bronchial:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
10	CTCF	chr4:10405440-10405590	GM12873	blood:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
11	CTCF	chr4:10405780-10405930	GM12874	blood:	n/a	n/a
12	CTCF	chr4:10405400-10405710	HepG2	liver:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
13	CTCF	chr4:10405385-10405775	GM12878	blood:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
14	CTCF	chr4:10405520-10405670	HVMF	connective:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
15	CTCF	chr4:10405467-10405686	Medullo	brain:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
16	CTCF	chr4:10405485-10405650	Hela-S3	cervix:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
17	CTCF	chr4:10405467-10405715	A549	lung:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
18	CTCF	chr4:10405400-10405550	HAc	cerebellar:	n/a	n/a
19	CTCF	chr4:10405858-10405928	LNCaP	prostate:	n/a	n/a
20	CTCF	chr4:10405480-10405630	SK-N-SH_RA	brain:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
21	CTCF	chr4:10405405-10405679	T-47D	breast:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
22	CTCF	chr4:10405480-10405630	GM12871	blood:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
23	CTCF	chr4:10405440-10405590	WI-38	lung:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
24	CTCF	chr4:10405440-10405590	HCM	heart:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
25	CTCF	chr4:10405400-10405550	GM12864	blood:	n/a	n/a
26	CTCF	chr4:10405500-10405650	HepG2	liver:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
27	CTCF	chr4:10407212-10407274	GM20000	blood:	n/a	n/a
28	CTCF	chr4:10405207-10405881	HCT-116	colon:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
29	CTCF	chr4:10405500-10405650	HRPEpiC	eye:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
30	CTCF	chr4:10405460-10405610	GM12869	blood:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
31	CTCF	chr4:10405464-10405691	GM12878	blood:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
32	CTCF	chr4:10405460-10405669	Lung_OC	lung:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
33	CTCF	chr4:10405520-10405670	GM12872	blood:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
34	CTCF	chr4:10405500-10405650	BE2_C	brain:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
35	CTCF	chr4:10405468-10405674	HepG2	liver:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
36	CTCF	chr4:10405240-10405390	HRPEpiC	eye:	n/a	n/a
37	CTCF	chr4:10405540-10405690	GM12864	blood:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
38	CTCF	chr4:10405480-10405630	GM12870	blood:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
39	CTCF	chr4:10405454-10405705	LNCaP	prostate:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
40	CTCF	chr4:10405500-10405650	GM12865	blood:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
41	CTCF	chr4:10405520-10405670	HMF	breast:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
42	CTCF	chr4:10405480-10405630	HMEC	breast:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
43	CTCF	chr4:10405480-10405630	AG09319	gingival:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
44	CTCF	chr4:10405480-10405630	HEEpiC	esophagus:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
45	CTCF	chr4:10405480-10405630	GM06990	blood:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
46	CTCF	chr4:10405227-10405935	A549	lung:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
47	CTCF	chr4:10405153-10405807	K562	blood:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
48	CTCF	chr4:10405480-10405630	HPAF	blood vessel:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
49	CTCF	chr4:10405500-10405650	AG04450	lung:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
50	CTCF	chr4:10405500-10405650	GM12872	blood:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:10405694-10405744	MCF10A-Er-Src	breast:	n/a
2	chr4:10405694-10405744	AG04450	lung:	fetal
3	chr4:10405694-10405744	HCT-116	colon:	n/a
4	chr4:10405694-10405744	HMEC	breast:	n/a
5	chr4:10405694-10405744	PFSK-1	brain:	n/a
6	chr4:10405694-10405744	HRPEpiC	eye:	n/a
7	chr4:10405694-10405744	Hepatocyte	liver:	n/a
8	chr4:10405694-10405744	HEEpiC	esophagus:	n/a
9	chr4:10405694-10405744	AG04449	skin:	fetal
10	chr4:10405694-10405744	PANC-1	pancreas:	n/a
11	chr4:10405694-10405744	HEK293	kidney:	embryo
12	chr4:10405694-10405744	AG10803	skin:	n/a
13	chr4:10405694-10405744	SK-N-SH	brain:	n/a
14	chr4:10405694-10405744	NHDF-neo	bronchial:	n/a
15	chr4:10405694-10405744	HCPEpiC	choroid plexus:	n/a
16	chr4:10405694-10405744	HCM	heart:	n/a
17	chr4:10405694-10405744	NH-A	brain:	n/a
18	chr4:10405694-10405744	AG09319	gingival:	n/a
19	chr4:10405694-10405744	AoSMC	blood vessel:	n/a
20	chr4:10405694-10405744	HIPEpiC	eye:	n/a
21	chr4:10405694-10405744	A549	lung:	n/a
22	chr4:10405694-10405744	GM12892	blood:	n/a
23	chr4:10405694-10405744	U87	brain:	n/a
24	chr4:10405694-10405744	GM06990	blood:	n/a
25	chr4:10405694-10405744	HAEpiC	amniotic membrane:	n/a
26	chr4:10405694-10405744	T-47D	breast:	n/a
27	chr4:10405694-10405744	NT2-D1	testis:	n/a
28	chr4:10405694-10405744	BJ	skin:	n/a
29	chr4:10405694-10405744	ProgFib	skin:	n/a
30	chr4:10405694-10405744	MCF-7	breast:	n/a
31	chr4:10405694-10405744	PrEC	prostate:	n/a
32	chr4:10405694-10405744	HL-60	blood:	n/a
33	chr4:10405694-10405744	ovcar-3	ovarian:	n/a
34	chr4:10405694-10405744	NHBE	bronchial:	n/a
35	chr4:10405694-10405744	CMK	blood:	n/a
36	chr4:10405694-10405744	NB4	blood:	n/a
37	chr4:10405694-10405744	BE2_C	brain:	n/a
38	chr4:10405694-10405744	SKMC	muscle:	n/a
39	chr4:10405694-10405744	HCF	heart:	n/a
40	chr4:10405694-10405744	K562	blood:	n/a
41	chr4:10405694-10405744	GM19239	blood:	n/a
42	chr4:10405694-10405744	GM12878	blood:	n/a
43	chr4:10405694-10405744	Hela-S3	cervix:	n/a
44	chr4:10405694-10405744	HUVEC	blood vessel:	n/a
45	chr4:10405694-10405744	HNPCEpiC	eye:	n/a
46	chr4:10405694-10405744	HepG2	liver:	n/a
47	chr4:10405694-10405744	AG09309	skin:	n/a
48	chr4:10405694-10405744	HRE	kidney:	n/a
49	chr4:10405694-10405744	GM12891	blood:	n/a
50	chr4:10405694-10405744	Caco-2	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:10181802..10184742-chr4:10401642..10403855,2	K562	blood:
2	chr4:10166196..10167366-chr4:10404929..10406035,4	MCF-7	breast:
3	chr4:10117259..10123841-chr4:10401893..10417202,19	K562	blood:
4	chr4:10184632..10187184-chr4:10400763..10402949,2	K562	blood:
5	chr4:10187220..10189194-chr4:10403510..10406450,3	K562	blood:
6	chr4:10158544..10160312-chr4:10404691..10406060,12	K562	blood:
7	chr4:10031896..10034212-chr4:10409451..10411616,2	K562	blood:
8	chr4:10179301..10181367-chr4:10408418..10410454,2	K562	blood:
9	chr4:10182452..10185153-chr4:10405566..10407454,2	K562	blood:
10	chr4:10194015..10194637-chr4:10405680..10406337,2	MCF-7	breast:
11	chr4:10117259..10119774-chr4:10404203..10405780,2	K562	blood:
12	chr4:10405058..10406722-chr4:10414024..10415781,2	K562	blood:
13	chr4:10180539..10184306-chr4:10401076..10403855,3	K562	blood:
14	chr4:10391155..10393700-chr4:10401011..10403355,4	MCF-7	breast:
15	chr4:10404962..10406013-chr4:10527520..10528737,3	MCF-7	breast:
16	chr4:10406734..10408445-chr4:10443381..10446084,2	K562	blood:
17	chr17:59945131..59945952-chr4:10405006..10405538,2	MCF-7	breast:
18	chr4:10186739..10189194-chr4:10403510..10406450,4	K562	blood:
19	chr4:10120437..10124442-chr4:10402726..10405362,4	K562	blood:
20	chr4:10172802..10175283-chr4:10404131..10407127,2	K562	blood:
21	chr4:10166236..10167092-chr4:10405236..10406016,3	MCF-7	breast:
22	chr4:10201021..10203569-chr4:10408297..10410976,2	K562	blood:
23	chr4:10185450..10187184-chr4:10401056..10402949,2	K562	blood:
24	chr4:10161526..10162602-chr4:10405096..10406350,5	K562	blood:
25	chr4:10187984..10188890-chr4:10405320..10406071,3	MCF-7	breast:
26	chr4:10159016..10159805-chr4:10405257..10406163,3	MCF-7	breast:
27	chr4:10166648..10168321-chr4:10402902..10405737,2	K562	blood:
28	chr4:10390019..10393146-chr4:10400722..10404569,4	K562	blood:
29	chr4:10166113..10167122-chr4:10405126..10405888,4	K562	blood:
30	chr4:10118696..10122262-chr4:10407294..10411909,5	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DRD5-4	chr4:10409553-10409610	FPKM1_group_22843_transcript_2
2	lnc-DRD5-4	chr4:10404495-10404649	FPKM1_group_22843_transcript_2
3	lnc-DRD5-4	chr4:10409553-10410132	NONHSAT095495
4	lnc-DRD5-4	chr4:10404495-10404649	NONHSAT095495

Variant related genes	Relation type
ENSG00000250613	TF binding region
ENSG00000250613	CpG island
ENSG00000248777	chromatin interactions
ENSG00000071127	chromatin interactions
ENSG00000223086	chromatin interactions

Extended variants
information (count: 520 )
Associated
traits (count: 51 )

Variant overlapped rSNPs/rCNVs (count:520 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs536009098	chr4:10398309-10398310	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs115374903	chr4:10398329-10398330	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs575975974	chr4:10398332-10398333	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs187638630	chr4:10398370-10398371	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs564826794	chr4:10398371-10398372	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs573137198	chr4:10398402-10398403	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs4389568	chr4:10398427-10398428	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs373123473	chr4:10398444-10398445	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs561845748	chr4:10398461-10398462	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs191502423	chr4:10398481-10398482	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs573043557	chr4:10398511-10398512	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs145399721	chr4:10398589-10398590	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs533666733	chr4:10398599-10398600	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs4698048	chr4:10398635-10398636	Weak transcription Enhancers Bivalent/Poised TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs73104904	chr4:10398690-10398691	Weak transcription Enhancers Bivalent/Poised TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs566793898	chr4:10398707-10398708	Weak transcription Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs149228919	chr4:10398751-10398752	Weak transcription Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs183566637	chr4:10398824-10398825	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs143235576	chr4:10398878-10398879	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs73104907	chr4:10398918-10398919	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs567349883	chr4:10398939-10398940	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs188055583	chr4:10398943-10398944	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs540056053	chr4:10399024-10399025	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs558155281	chr4:10399056-10399057	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs573530264	chr4:10399066-10399067	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs192815369	chr4:10399067-10399068	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs4599407	chr4:10399068-10399069	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs184527509	chr4:10399088-10399089	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs186616893	chr4:10399093-10399094	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs4604051	chr4:10399096-10399097	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs543859738	chr4:10399109-10399110	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs73104910	chr4:10399133-10399134	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs73224473	chr4:10399173-10399174	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs577650526	chr4:10399242-10399243	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs560140604	chr4:10399292-10399293	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs73104913	chr4:10399316-10399317	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs369718549	chr4:10399338-10399339	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs548964211	chr4:10399380-10399381	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs567292233	chr4:10399386-10399387	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs113546158	chr4:10399438-10399439	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs35427072	chr4:10399456-10399457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs55885405	chr4:10399465-10399466	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs147877508	chr4:10399495-10399496	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs141604649	chr4:10399513-10399514	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs571404714	chr4:10399518-10399519	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs539640015	chr4:10399520-10399521	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs545117245	chr4:10399521-10399522	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs147065703	chr4:10399570-10399571	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs534643805	chr4:10399576-10399577	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs534526707	chr4:10399580-10399581	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:51)

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

Chromatin state (count:36 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:10387000-10403600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr4:10396800-10399600	Enhancers	HMEC	breast
3	chr4:10397000-10399000	Enhancers	NHEK	skin
4	chr4:10397000-10400000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr4:10397200-10399200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr4:10397400-10398400	Enhancers	K562	blood
7	chr4:10397600-10399000	Enhancers	Fetal Thymus	thymus
8	chr4:10397800-10398400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
9	chr4:10398400-10403400	Weak transcription	K562	blood
10	chr4:10398600-10398800	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle
11	chr4:10399000-10405600	Weak transcription	NHEK	skin
12	chr4:10399200-10402800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr4:10399600-10400000	Weak transcription	HMEC	breast
14	chr4:10400000-10400400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr4:10400000-10400600	Enhancers	HMEC	breast
16	chr4:10400400-10400600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr4:10400600-10405200	Weak transcription	HMEC	breast
18	chr4:10400600-10405400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr4:10402800-10403000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr4:10403400-10406000	Enhancers	K562	blood
21	chr4:10405200-10405800	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr4:10405200-10406000	Enhancers	HMEC	breast
23	chr4:10405400-10406000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr4:10405600-10406000	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr4:10405600-10406000	Enhancers	NHEK	skin
26	chr4:10405600-10406400	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr4:10406000-10408800	Weak transcription	K562	blood
28	chr4:10407400-10407600	Enhancers	Fetal Heart	heart
29	chr4:10407600-10408600	Weak transcription	Fetal Heart	heart
30	chr4:10408200-10408600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr4:10408600-10410600	Enhancers	Fetal Heart	heart
32	chr4:10408600-10421000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr4:10408800-10409200	Enhancers	Gastric	stomach
34	chr4:10408800-10410200	Enhancers	K562	blood
35	chr4:10409400-10410800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr4:10409400-10410800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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