Variant report

Variant	nsv1021433
Chromosome Location	chr6:163375760-163509866
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:296)
CpG islands
(count:305)
Chromatin interactive
region (count:11)
LncRNA
region (count:20)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:296 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr6:163422341-163422769	GM12878	blood:	n/a	n/a
2	BATF	chr6:163422365-163422747	GM12878	blood:	n/a	chr6:163422593-163422603
3	BATF	chr6:163422337-163422713	GM12878	blood:	n/a	chr6:163422593-163422603
4	BCL11A	chr6:163422413-163422668	GM12878	blood:	n/a	n/a
5	BCL11A	chr6:163422425-163422741	GM12878	blood:	n/a	n/a
6	BCL3	chr6:163476237-163476563	GM12878	blood:	n/a	n/a
7	BCL3	chr6:163479336-163479590	GM12878	blood:	n/a	n/a
8	BCL3	chr6:163476202-163476485	GM12878	blood:	n/a	n/a
9	BCL3	chr6:163479255-163479599	GM12878	blood:	n/a	n/a
10	CBX3	chr6:163453013-163453248	K562	blood:	n/a	n/a
11	CBX3	chr6:163385655-163386353	HCT-116	colon:	n/a	n/a
12	CBX3	chr6:163385583-163386388	HCT-116	colon:	n/a	n/a
13	CCNT2	chr6:163484404-163484537	K562	blood:	n/a	n/a
14	CEBPB	chr6:163442088-163442410	HepG2	liver:	n/a	chr6:163442250-163442261
15	CEBPB	chr6:163478324-163478696	IMR90	lung:	n/a	chr6:163478503-163478514
16	CEBPB	chr6:163478428-163478563	HepG2	liver:	n/a	chr6:163478503-163478514
17	CEBPB	chr6:163385746-163386445	HCT-116	colon:	n/a	n/a
18	CEBPB	chr6:163462678-163462805	HepG2	liver:	n/a	chr6:163462716-163462727 chr6:163462715-163462728 chr6:163462715-163462726 chr6:163462717-163462726 chr6:163462717-163462726 chr6:163462717-163462726 chr6:163462717-163462726
19	CEBPB	chr6:163478318-163478693	HepG2	liver:	n/a	chr6:163478503-163478514
20	CEBPB	chr6:163478331-163478677	MCF-7	breast:	n/a	chr6:163478503-163478514
21	CEBPB	chr6:163478280-163478773	A549	lung:	n/a	chr6:163478503-163478514
22	CEBPB	chr6:163385672-163386327	HCT-116	colon:	n/a	n/a
23	CEBPB	chr6:163385817-163386320	IMR90	lung:	n/a	n/a
24	CEBPB	chr6:163478305-163478612	K562	blood:	n/a	chr6:163478503-163478514
25	CEBPB	chr6:163443243-163443443	HepG2	liver:	n/a	chr6:163443336-163443347
26	CEBPB	chr6:163478317-163478694	K562	blood:	n/a	chr6:163478503-163478514
27	CEBPB	chr6:163478329-163478613	A549	lung:	n/a	chr6:163478503-163478514
28	CEBPB	chr6:163478322-163478694	A549	lung:	n/a	chr6:163478503-163478514
29	CEBPB	chr6:163442138-163442402	A549	lung:	n/a	chr6:163442250-163442261
30	CEBPB	chr6:163478412-163478549	K562	blood:	n/a	chr6:163478503-163478514
31	CEBPB	chr6:163478322-163478698	H1-hESC	embryonic stem cell:	n/a	chr6:163478503-163478514
32	CEBPB	chr6:163478376-163478685	ECC-1	luminal epithelium:	n/a	chr6:163478503-163478514
33	CEBPB	chr6:163384837-163385142	IMR90	lung:	n/a	n/a
34	CTCF	chr6:163462440-163462590	HEK293	kidney:	n/a	n/a
35	CTCF	chr6:163385660-163385810	NHDF-neo	bronchial:	n/a	n/a
36	CTCF	chr6:163475280-163475430	GM12867	blood:	n/a	n/a
37	CTCF	chr6:163437133-163437222	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr6:163434560-163434710	SK-N-SH_RA	brain:	n/a	n/a
39	CTCF	chr6:163484300-163484450	GM12878	blood:	n/a	n/a
40	CTCF	chr6:163485536-163485560	Fibrobl	skin:	n/a	n/a
41	CTCF	chr6:163405131-163405173	LNCaP	prostate:	n/a	n/a
42	CTCF	chr6:163398907-163398925	LNCaP	prostate:	n/a	n/a
43	CTCF	chr6:163458799-163458848	Fibrobl	skin:	n/a	n/a
44	CTCF	chr6:163437360-163437510	NHEK	skin:	n/a	chr6:163437496-163437503
45	CTCF	chr6:163499800-163499950	GM12867	blood:	n/a	chr6:163499881-163499889
46	CTCF	chr6:163504910-163504982	GM20000	blood:	n/a	n/a
47	E2F4	chr6:163504931-163505302	MCF10A-Er-Src	breast:	n/a	n/a
48	E2F4	chr6:163489734-163490095	MCF10A-Er-Src	breast:	n/a	n/a
49	E2F4	chr6:163426149-163426477	MCF10A-Er-Src	breast:	n/a	n/a
50	E2F4	chr6:163385218-163385631	MCF10A-Er-Src	breast:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:163475324-163475374	HL-60	blood:	n/a
2	chr6:163475718-163475768	HEK293	kidney:	embryo
3	chr6:163475252-163475302	CMK	blood:	n/a
4	chr6:163475252-163475302	A549	lung:	n/a
5	chr6:163506790-163506840	HIPEpiC	eye:	n/a
6	chr6:163506790-163506840	PANC-1	pancreas:	n/a
7	chr6:163475718-163475768	HCPEpiC	choroid plexus:	n/a
8	chr6:163475333-163475383	NH-A	brain:	n/a
9	chr6:163475718-163475768	HMEC	breast:	n/a
10	chr6:163475718-163475768	U87	brain:	n/a
11	chr6:163475718-163475768	ECC-1	luminal epithelium:	n/a
12	chr6:163475252-163475302	AG09309	skin:	n/a
13	chr6:163475252-163475302	AoSMC	blood vessel:	n/a
14	chr6:163475333-163475383	HRPEpiC	eye:	n/a
15	chr6:163475333-163475383	H1-hESC	embryonic stem cell:	embryo
16	chr6:163475324-163475374	HEK293	kidney:	embryo
17	chr6:163475324-163475374	U87	brain:	n/a
18	chr6:163475324-163475374	Hepatocyte	liver:	n/a
19	chr6:163475252-163475302	HCPEpiC	choroid plexus:	n/a
20	chr6:163475718-163475768	IMR90	lung:	fetal
21	chr6:163475252-163475302	GM12892	blood:	n/a
22	chr6:163506790-163506840	BJ	skin:	n/a
23	chr6:163475252-163475302	SK-N-SH	brain:	n/a
24	chr6:163475252-163475302	NHDF-neo	bronchial:	n/a
25	chr6:163475333-163475383	PFSK-1	brain:	n/a
26	chr6:163475333-163475383	SKMC	muscle:	n/a
27	chr6:163475333-163475383	LNCaP	prostate:	n/a
28	chr6:163475718-163475768	AG09309	skin:	n/a
29	chr6:163506790-163506840	ovcar-3	ovarian:	n/a
30	chr6:163475718-163475768	Hela-S3	cervix:	n/a
31	chr6:163475324-163475374	RPTEC	kidney:	n/a
32	chr6:163475324-163475374	HRE	kidney:	n/a
33	chr6:163475333-163475383	NHBE	bronchial:	n/a
34	chr6:163475324-163475374	HCT-116	colon:	n/a
35	chr6:163475252-163475302	HPAEpiC	pulmonary alveolar:	n/a
36	chr6:163506790-163506840	AG09319	gingival:	n/a
37	chr6:163475252-163475302	HepG2	liver:	n/a
38	chr6:163475333-163475383	U87	brain:	n/a
39	chr6:163475324-163475374	AG10803	skin:	n/a
40	chr6:163475718-163475768	PrEC	prostate:	n/a
41	chr6:163475333-163475383	HPAEpiC	pulmonary alveolar:	n/a
42	chr6:163475333-163475383	HMEC	breast:	n/a
43	chr6:163475324-163475374	H1-hESC	embryonic stem cell:	embryo
44	chr6:163475718-163475768	AG04449	skin:	fetal
45	chr6:163475252-163475302	HCT-116	colon:	n/a
46	chr6:163475333-163475383	NT2-D1	testis:	n/a
47	chr6:163475324-163475374	SAEC	small airway:	n/a
48	chr6:163475324-163475374	PrEC	prostate:	n/a
49	chr6:163475324-163475374	GM19239	blood:	n/a
50	chr6:163506790-163506840	GM06990	blood:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:163458107..163459739-chr6:163463183..163466142,2	K562	blood:
2	chr6:163509761..163512247-chr6:163514199..163516689,2	K562	blood:
3	chr12:104252627..104253426-chr6:163440642..163441162,2	MCF-7	breast:
4	chr6:163426091..163427659-chr6:163429418..163431049,2	K562	blood:
5	chr6:163429068..163430008-chrX:51497389..51498171,2	MCF-7	breast:
6	chr6:163467143..163469243-chr6:163471356..163474324,2	K562	blood:
7	chr6:163467143..163469243-chr6:163471356..163474324,2	K562	blood:
8	chr6:163383289..163384996-chr6:163389712..163391752,2	MCF-7	breast:
9	chr6:163458107..163459739-chr6:163463183..163466142,2	K562	blood:
10	chr6:163383289..163384996-chr6:163389712..163391752,2	MCF-7	breast:
11	chr6:163426091..163427659-chr6:163429418..163431049,2	K562	blood:

(count:20 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AL078585.1-1	chr6:163464011-163464201	ENSG00000225437.1
2	lnc-AL078585.1-13	chr6:163394947-163395183	ucscGeneNc_uc003qud_1
3	lnc-AL078585.1-14	chr6:163378290-163378580	NONHSAT115947
4	lnc-AL078585.1-1	chr6:163464086-163464201	ENSG00000225437.1
5	lnc-AL078585.1-1	chr6:163474957-163475193	ENSG00000225437.1
6	lnc-AL078585.1-13	chr6:163392282-163393054	ucscGeneNc_uc003qud_1
7	lnc-AL078585.1-1	chr6:163463589-163463729	ENSG00000225437.1
8	lnc-AL078585.1-1	chr6:163467616-163467715	ENSG00000225437.1
9	lnc-AL078585.1-1	chr6:163472292-163473064	ENSG00000225437.1
10	lnc-AL078585.1-1	chr6:163465681-163465778	ENSG00000225437.1
11	lnc-AL078585.1-1	chr6:163474957-163475173	NONHSAT115951
12	lnc-AL078585.1-13	chr6:163384002-163384191	ucscGeneNc_uc003qud_1
13	lnc-AL078585.1-1	chr6:163472292-163472446	ENSG00000225437.1
14	lnc-AL078585.1-1	chr6:163467647-163467715	NONHSAT115951
15	lnc-AL078585.1-1	chr6:163464012-163464201	ENSG00000225437.1
16	lnc-AL078585.1-1	chr6:163471578-163473064	NONHSAT115951
17	lnc-AL078585.1-1	chr6:163467616-163467715	ENSG00000225437.1
18	lnc-AL078585.1-13	chr6:163387606-163387705	ucscGeneNc_uc003qud_1
19	lnc-AL078585.1-1	chr6:163467616-163467717	ENSG00000225437.1
20	lnc-AL078585.1-1	chr6:163465681-163465778	ENSG00000225437.1

No data

Variant related genes	Relation type
ENSG00000225437	TF binding region
PACRG	TF binding region
ENSG00000217557	TF binding region
ENSG00000225437	CpG island
PACRG	CpG island
ENSG00000217557	CpG island
ENSG00000225437	chromatin interactions

Extended variants
information (count: 3151 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:3151 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs368874776	chr6:163377207-163377208	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
2	rs372559360	chr6:163377235-163377236	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs372750196	chr6:163377236-163377237	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs576265814	chr6:163377271-163377272	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs537956776	chr6:163377277-163377278	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs555093104	chr6:163377358-163377359	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs561036915	chr6:163377359-163377360	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs574830838	chr6:163377368-163377369	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs540660261	chr6:163377399-163377400	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs141304699	chr6:163377419-163377420	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs577142625	chr6:163377428-163377429	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs185448105	chr6:163377436-163377437	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs562750586	chr6:163377540-163377541	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs376991690	chr6:163377545-163377546	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs531883630	chr6:163377556-163377557	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs75751827	chr6:163377567-163377568	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs189570893	chr6:163377592-163377593	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs180824541	chr6:163377622-163377623	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs369802100	chr6:163377623-163377624	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs373568731	chr6:163377704-163377705	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs375578397	chr6:163377705-163377706	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs570432479	chr6:163377742-163377743	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs146183182	chr6:163377832-163377833	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs185881571	chr6:163377844-163377845	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs137882437	chr6:163377852-163377853	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs569849667	chr6:163377887-163377888	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs386708097	chr6:163377906-163377907	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs572806693	chr6:163377923-163377924	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs190253555	chr6:163377928-163377929	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs181112083	chr6:163377942-163377943	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs540334425	chr6:163377944-163377945	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs565041706	chr6:163377983-163377984	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs142499642	chr6:163378037-163378038	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs534010026	chr6:163378068-163378069	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs553767580	chr6:163378077-163378078	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs73607813	chr6:163378084-163378085	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs546090247	chr6:163378098-163378099	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs562887943	chr6:163378119-163378120	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs576652465	chr6:163378139-163378140	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs186149177	chr6:163378163-163378164	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs75392391	chr6:163378183-163378184	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs12194418	chr6:163378215-163378216	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs527402456	chr6:163378253-163378254	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs541092311	chr6:163378265-163378266	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs564074699	chr6:163378286-163378287	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs7765189	chr6:163378291-163378292	Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs549794023	chr6:163378307-163378308	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
48	rs145964791	chr6:163378322-163378323	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
49	rs529157144	chr6:163378337-163378338	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
50	rs549184326	chr6:163378365-163378366	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Testicular germ cell tumor	18059402	CNVD
Developmental delay	21147756	CNVD
Chordoma	18071362	CNVD
Myelofibrosis	22110671	CNVD
Autism	22241247	CNVD
Breast cancer	16397240	CNVD
Atherosclerosis	21956041	CNVD
Maculopathy	20981449	CNVD
Retinoblastoma	22278416	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Ovarian cancer	20844748	CNVD
Uveal melanoma	20484589	CNVD
Glioblastoma multiforme	19435819	CNVD
Astrocytoma	16205629	CNVD
Parkinson disease	17160897	CNVD
Ovarian cancer	21720365	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian cancer	22355333	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
abnormal development	18461090	CNVD
Cancer	20164919	CNVD

Chromatin state (count:361 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:163377200-163377400	Bivalent Enhancer	Fetal Heart	heart
2	chr6:163377400-163379800	Enhancers	Fetal Heart	heart
3	chr6:163378200-163378600	Enhancers	Right Atrium	heart
4	chr6:163378600-163380800	Weak transcription	Right Atrium	heart
5	chr6:163381400-163384200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr6:163381400-163384200	Enhancers	NHDF-Ad	bronchial
7	chr6:163381600-163382000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr6:163382000-163382200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr6:163382200-163382600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr6:163382600-163383000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr6:163382600-163383800	Enhancers	Muscle Satellite Cultured Cells	--
12	chr6:163382600-163383800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr6:163382800-163383600	Enhancers	NHLF	lung
14	chr6:163383000-163383600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr6:163383000-163383600	Enhancers	Osteobl	bone
16	chr6:163383000-163384200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr6:163383000-163386400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr6:163383000-163386400	Enhancers	NHEK	skin
19	chr6:163383200-163383800	Enhancers	NH-A	brain
20	chr6:163383200-163384200	Enhancers	HSMM	muscle
21	chr6:163383600-163384000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr6:163383600-163384800	Weak transcription	NHLF	lung
23	chr6:163383600-163385000	Weak transcription	Osteobl	bone
24	chr6:163383800-163384800	Weak transcription	Muscle Satellite Cultured Cells	--
25	chr6:163383800-163385000	Weak transcription	NH-A	brain
26	chr6:163383800-163385600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr6:163384000-163387000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr6:163384200-163384600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr6:163384200-163384600	Weak transcription	HSMM	muscle
30	chr6:163384200-163384600	Weak transcription	NHDF-Ad	bronchial
31	chr6:163384200-163385400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr6:163384600-163386800	Enhancers	HSMM	muscle
33	chr6:163384600-163387000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr6:163384600-163387400	Enhancers	NHDF-Ad	bronchial
35	chr6:163384800-163385400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr6:163384800-163385400	Enhancers	Muscle Satellite Cultured Cells	--
37	chr6:163384800-163387200	Enhancers	NHLF	lung
38	chr6:163385000-163385800	Enhancers	Osteobl	bone
39	chr6:163385000-163386400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr6:163385000-163386600	Enhancers	HSMMtube	muscle
41	chr6:163385000-163386600	Enhancers	NH-A	brain
42	chr6:163385200-163386400	Enhancers	Fetal Heart	heart
43	chr6:163385200-163386600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr6:163385400-163385800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr6:163385400-163385800	Flanking Active TSS	Muscle Satellite Cultured Cells	--
46	chr6:163385400-163386400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr6:163385400-163386400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr6:163385400-163386600	Enhancers	Fetal Muscle Leg	muscle
49	chr6:163385400-163386600	Enhancers	Fetal Stomach	stomach
50	chr6:163385600-163386200	Enhancers	Adipose Nuclei	Adipose

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