Variant report

Variant	nsv5250
Chromosome Location	chr6:33565017-33598370
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1201)
CpG islands
(count:1344)
Chromatin interactive
region (count:64)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1201 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:33581113-33581503	HepG2	liver:	n/a	n/a
2	ATF2	chr6:33564809-33565065	GM12878	blood:	n/a	n/a
3	BACH1	chr6:33576845-33577141	K562	blood:	n/a	n/a
4	BACH1	chr6:33589863-33589941	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr6:33574858-33575263	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr6:33589210-33589636	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr6:33590893-33591071	GM12878	blood:	n/a	n/a
8	BHLHE40	chr6:33588787-33589175	GM12878	blood:	n/a	n/a
9	BHLHE40	chr6:33589438-33589557	K562	blood:	n/a	n/a
10	BHLHE40	chr6:33588743-33588841	K562	blood:	n/a	n/a
11	BHLHE40	chr6:33581084-33581617	HepG2	liver:	n/a	n/a
12	BHLHE40	chr6:33575607-33575970	HepG2	liver:	n/a	n/a
13	BRCA1	chr6:33578894-33579259	Hela-S3	cervix:	n/a	n/a
14	BRCA1	chr6:33588000-33588122	GM12878	blood:	n/a	n/a
15	BRCA1	chr6:33577012-33577175	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr6:33581189-33581381	HepG2	liver:	n/a	n/a
17	CBX3	chr6:33575421-33575808	K562	blood:	n/a	n/a
18	CBX3	chr6:33575304-33575966	HCT-116	colon:	n/a	n/a
19	CBX3	chr6:33575277-33576048	HCT-116	colon:	n/a	n/a
20	CBX3	chr6:33588449-33589158	K562	blood:	n/a	n/a
21	CCNT2	chr6:33584824-33585044	K562	blood:	n/a	n/a
22	CCNT2	chr6:33588608-33589696	K562	blood:	n/a	n/a
23	CEBPB	chr6:33588353-33588695	H1-hESC	embryonic stem cell:	n/a	chr6:33588550-33588559 chr6:33588550-33588559 chr6:33588550-33588559 chr6:33588549-33588560 chr6:33588550-33588559
24	CEBPB	chr6:33590991-33591326	IMR90	lung:	n/a	chr6:33591159-33591170
25	CEBPB	chr6:33584733-33585105	K562	blood:	n/a	chr6:33584857-33584868
26	CEBPB	chr6:33584744-33584990	K562	blood:	n/a	chr6:33584857-33584868
27	CEBPB	chr6:33588358-33588743	K562	blood:	n/a	chr6:33588550-33588559 chr6:33588550-33588559 chr6:33588550-33588559 chr6:33588549-33588560 chr6:33588550-33588559
28	CEBPB	chr6:33584639-33585116	Hela-S3	cervix:	n/a	chr6:33584857-33584868
29	CEBPB	chr6:33588174-33588710	ECC-1	luminal epithelium:	n/a	chr6:33588550-33588559 chr6:33588550-33588559 chr6:33588550-33588559 chr6:33588549-33588560 chr6:33588550-33588559
30	CEBPB	chr6:33581076-33581450	HepG2	liver:	n/a	n/a
31	CEBPB	chr6:33591034-33591321	K562	blood:	n/a	chr6:33591159-33591170
32	CEBPB	chr6:33591121-33591323	HepG2	liver:	n/a	chr6:33591159-33591170
33	CEBPB	chr6:33588251-33589583	Hela-S3	cervix:	n/a	chr6:33588550-33588559 chr6:33588550-33588559 chr6:33588550-33588559 chr6:33588549-33588560 chr6:33588550-33588559
34	CEBPB	chr6:33584690-33585038	IMR90	lung:	n/a	chr6:33584857-33584868
35	CEBPB	chr6:33588359-33588710	HepG2	liver:	n/a	chr6:33588550-33588559 chr6:33588550-33588559 chr6:33588550-33588559 chr6:33588549-33588560 chr6:33588550-33588559
36	CEBPB	chr6:33584758-33584987	A549	lung:	n/a	chr6:33584857-33584868
37	CEBPB	chr6:33578946-33579529	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr6:33577992-33578355	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr6:33581183-33581388	HepG2	liver:	n/a	n/a
40	CEBPB	chr6:33567107-33567639	ECC-1	luminal epithelium:	n/a	n/a
41	CEBPB	chr6:33588322-33588675	K562	blood:	n/a	chr6:33588550-33588559 chr6:33588550-33588559 chr6:33588550-33588559 chr6:33588549-33588560 chr6:33588550-33588559
42	CEBPB	chr6:33566321-33566370	A549	lung:	n/a	n/a
43	CEBPB	chr6:33591019-33591279	A549	lung:	n/a	chr6:33591159-33591170
44	CEBPB	chr6:33590766-33591353	Hela-S3	cervix:	n/a	chr6:33591159-33591170
45	CEBPB	chr6:33581040-33581472	HepG2	liver:	n/a	n/a
46	CEBPB	chr6:33588358-33588713	A549	lung:	n/a	chr6:33588550-33588559 chr6:33588550-33588559 chr6:33588550-33588559 chr6:33588549-33588560 chr6:33588550-33588559
47	CEBPB	chr6:33584793-33584995	HepG2	liver:	n/a	chr6:33584857-33584868
48	CEBPB	chr6:33588361-33588727	IMR90	lung:	n/a	chr6:33588550-33588559 chr6:33588550-33588559 chr6:33588550-33588559 chr6:33588549-33588560 chr6:33588550-33588559
49	CEBPB	chr6:33588316-33588671	ECC-1	luminal epithelium:	n/a	chr6:33588550-33588559 chr6:33588550-33588559 chr6:33588550-33588559 chr6:33588549-33588560 chr6:33588550-33588559
50	CEBPB	chr6:33584686-33585068	K562	blood:	n/a	chr6:33584857-33584868

(count:1344 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:33589019-33589069	AG09309	skin:	n/a
2	chr6:33589118-33589168	NT2-D1	testis:	n/a
3	chr6:33589019-33589069	AG09309	skin:	n/a
4	chr6:33589118-33589168	NT2-D1	testis:	n/a
5	chr6:33589118-33589168	HEEpiC	esophagus:	n/a
6	chr6:33589691-33589741	GM19239	blood:	n/a
7	chr6:33595160-33595210	NB4	blood:	n/a
8	chr6:33592658-33592708	AG04450	lung:	fetal
9	chr6:33575719-33575769	GM12892	blood:	n/a
10	chr6:33598003-33598053	HPAEpiC	pulmonary alveolar:	n/a
11	chr6:33589061-33589111	CMK	blood:	n/a
12	chr6:33589030-33589080	HRPEpiC	eye:	n/a
13	chr6:33588302-33588352	GM06990	blood:	n/a
14	chr6:33587496-33587546	BE2_C	brain:	n/a
15	chr6:33577711-33577761	Hepatocyte	liver:	n/a
16	chr6:33587496-33587546	PANC-1	pancreas:	n/a
17	chr6:33585071-33585121	NB4	blood:	n/a
18	chr6:33585071-33585121	RPTEC	kidney:	n/a
19	chr6:33589030-33589080	SK-N-MC	brain:	n/a
20	chr6:33598003-33598053	HIPEpiC	eye:	n/a
21	chr6:33589131-33589181	MCF10A-Er-Src	breast:	n/a
22	chr6:33588219-33588269	HRPEpiC	eye:	n/a
23	chr6:33587496-33587546	MCF-7	breast:	n/a
24	chr6:33595160-33595210	LNCaP	prostate:	n/a
25	chr6:33588219-33588269	PrEC	prostate:	n/a
26	chr6:33577711-33577761	NH-A	brain:	n/a
27	chr6:33590458-33590508	NH-A	brain:	n/a
28	chr6:33588932-33588982	HNPCEpiC	eye:	n/a
29	chr6:33589418-33589468	Caco-2	colon:	n/a
30	chr6:33588219-33588269	NT2-D1	testis:	n/a
31	chr6:33595160-33595210	SK-N-SH_RA	brain:	n/a
32	chr6:33589418-33589468	AoSMC	blood vessel:	n/a
33	chr6:33588932-33588982	HCM	heart:	n/a
34	chr6:33589118-33589168	AoSMC	blood vessel:	n/a
35	chr6:33589691-33589741	HCF	heart:	n/a
36	chr6:33588944-33588994	MCF10A-Er-Src	breast:	n/a
37	chr6:33589019-33589069	HEEpiC	esophagus:	n/a
38	chr6:33589019-33589069	NH-A	brain:	n/a
39	chr6:33589131-33589181	LNCaP	prostate:	n/a
40	chr6:33588944-33588994	HMEC	breast:	n/a
41	chr6:33589418-33589468	GM06990	blood:	n/a
42	chr6:33588932-33588982	AG04449	skin:	fetal
43	chr6:33577711-33577761	PrEC	prostate:	n/a
44	chr6:33588944-33588994	HUVEC	blood vessel:	n/a
45	chr6:33588944-33588994	ECC-1	luminal epithelium:	n/a
46	chr6:33588932-33588982	AG09319	gingival:	n/a
47	chr6:33589030-33589080	T-47D	breast:	n/a
48	chr6:33589061-33589111	BJ	skin:	n/a
49	chr6:33577711-33577761	Caco-2	colon:	n/a
50	chr6:33598003-33598053	Hepatocyte	liver:	n/a

(count:64 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:33577318..33579921-chr6:33582665..33584246,2	K562	blood:
2	chr6:33578081..33580623-chr6:33585899..33589337,3	K562	blood:
3	chr6:33546546..33549178-chr6:33588334..33590241,2	K562	blood:
4	chr6:33581288..33583329-chr6:33600315..33602072,2	K562	blood:
5	chr6:33594027..33596927-chr6:33599242..33602574,3	MCF-7	breast:
6	chr6:33587647..33590168-chr6:33590912..33595599,6	MCF-7	breast:
7	chr6:33574216..33577618-chr6:33579266..33582393,4	MCF-7	breast:
8	chr6:33562478..33565325-chr6:33572841..33575005,2	MCF-7	breast:
9	chr6:13574530..13575381-chr6:33588931..33589769,3	Hela-S3	cervix:
10	chr6:33588748..33590595-chr6:33677611..33680104,2	K562	blood:
11	chr6:33576666..33582891-chr6:33586745..33591603,10	MCF-7	breast:
12	chr6:33559755..33561474-chr6:33565706..33568231,2	K562	blood:
13	chr6:33561930..33564001-chr6:33577360..33579939,2	K562	blood:
14	chr6:33567572..33569907-chr6:33573549..33575919,2	MCF-7	breast:
15	chr6:33556929..33558055-chr6:33575240..33576451,8	MCF-7	breast:
16	chr1:149223926..149224778-chr6:33589055..33589566,2	Hela-S3	cervix:
17	chr6:33556929..33561530-chr6:33563084..33565973,5	MCF-7	breast:
18	chr6:33587667..33592228-chr6:33677016..33679936,5	MCF-7	breast:
19	chr6:33566688..33568911-chr6:33636835..33638571,2	K562	blood:
20	chr6:33567572..33569907-chr6:33573549..33575919,2	MCF-7	breast:
21	chr17:56735246..56737826-chr6:33586590..33589099,2	MCF-7	breast:
22	chr6:33587934..33590771-chr6:33596242..33598173,4	MCF-7	breast:
23	chr15:73925194..73925924-chr6:33589142..33589802,2	Hela-S3	cervix:
24	chr6:33590320..33593181-chr6:33667665..33670096,2	MCF-7	breast:
25	chr6:33587976..33588692-chr7:152372698..152373478,2	Hela-S3	cervix:
26	chr6:33574216..33577618-chr6:33579266..33582393,4	MCF-7	breast:
27	chr6:33550022..33555745-chr6:33586647..33590467,5	MCF-7	breast:
28	chr17:44270863..44271390-chr6:33589321..33590284,2	Hela-S3	cervix:
29	chr14:75745307..75745924-chr6:33588441..33589108,2	Hela-S3	cervix:
30	chr6:33382580..33384156-chr6:33587956..33590051,2	K562	blood:
31	chr17:56736454..56738602-chr6:33589465..33592275,2	MCF-7	breast:
32	chr6:33556983..33559426-chr6:33569915..33571800,2	MCF-7	breast:
33	chr6:33591444..33593471-chr6:33595633..33598243,2	MCF-7	breast:
34	chr6:33386588..33389201-chr6:33584352..33586241,2	MCF-7	breast:
35	chr18:18691523..18692461-chr6:33588062..33589054,2	Hela-S3	cervix:
36	chr6:33567331..33570244-chr6:33587818..33589464,2	MCF-7	breast:
37	chr1:155231631..155232403-chr6:33588518..33589463,2	Hela-S3	cervix:
38	chr6:33576269..33579262-chr6:33600060..33601906,2	MCF-7	breast:
39	chr6:33591444..33593471-chr6:33595633..33598243,2	MCF-7	breast:
40	chr6:33562478..33565325-chr6:33572841..33575005,2	MCF-7	breast:
41	chr12:53297626..53300477-chr6:33588925..33590822,2	MCF-7	breast:
42	chr6:33587172..33590152-chr6:34203876..34205466,2	K562	blood:
43	chr6:33557935..33558471-chr6:33567388..33568017,2	MCF-7	breast:
44	chr6:33596598..33599064-chr6:33678282..33680140,2	K562	blood:
45	chr6:33577318..33579921-chr6:33582665..33584246,2	K562	blood:
46	chr19:11491411..11492183-chr6:33588219..33588815,2	Hela-S3	cervix:
47	chr6:33557038..33558663-chr6:33565418..33568204,3	K562	blood:
48	chr6:33561576..33563352-chr6:33589353..33591952,2	K562	blood:
49	chr6:33586212..33588848-chr6:33589323..33592935,3	K562	blood:
50	chr1:93544219..93545082-chr6:33588370..33589018,2	Hela-S3	cervix:

No data

Variant related genes	Relation type
LINC00336	TF binding region
ITPR3	TF binding region
LINC00336	CpG island
ITPR3	CpG island
ENSG00000096433	chromatin interactions
ENSG00000223501	chromatin interactions
ENSG00000156642	chromatin interactions
ENSG00000030110	chromatin interactions
ENSG00000116521	chromatin interactions
ENSG00000231500	chromatin interactions
ENSG00000206737	chromatin interactions
ENSG00000137309	chromatin interactions
ENSG00000187266	chromatin interactions
ENSG00000197251	chromatin interactions
ENSG00000170345	chromatin interactions
ENSG00000120071	chromatin interactions
ENSG00000204188	chromatin interactions
ENSG00000170421	chromatin interactions
ENSG00000165891	chromatin interactions
ENSG00000197283	chromatin interactions
ENSG00000143033	chromatin interactions
ENSG00000112511	chromatin interactions
ENSG00000124523	chromatin interactions
ENSG00000067900	chromatin interactions
ENSG00000202077	chromatin interactions
ENSG00000137288	chromatin interactions
ENSG00000196584	chromatin interactions
ENSG00000214401	chromatin interactions

Extended variants
information (count: 1349 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:1349 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs55844831	chr6:33565017-33565018	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs71565392	chr6:33565047-33565048	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs545116110	chr6:33565051-33565052	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs560149903	chr6:33565052-33565053	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs575965715	chr6:33565058-33565059	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs527289176	chr6:33565094-33565095	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs62407594	chr6:33565098-33565099	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs115542012	chr6:33565100-33565101	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs531870589	chr6:33565147-33565148	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs558310683	chr6:33565153-33565154	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs150164382	chr6:33565158-33565159	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs115912459	chr6:33565260-33565261	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs76551673	chr6:33565271-33565272	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs79479600	chr6:33565330-33565331	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs536273796	chr6:33565359-33565360	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs191572622	chr6:33565391-33565392	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs62407595	chr6:33565406-33565407	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs493871	chr6:33565474-33565475	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs114998333	chr6:33565480-33565481	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs577918944	chr6:33565520-33565521	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs545139744	chr6:33565557-33565558	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs3846856	chr6:33565564-33565565	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs146770464	chr6:33565678-33565679	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs3846857	chr6:33565697-33565698	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs560918777	chr6:33565727-33565728	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs140328957	chr6:33565769-33565770	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs547245949	chr6:33565810-33565811	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs573700707	chr6:33565850-33565851	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs145417415	chr6:33565851-33565852	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs375860258	chr6:33565856-33565857	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs3857560	chr6:33565902-33565903	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs3846858	chr6:33565950-33565951	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs544196891	chr6:33565966-33565967	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs536727251	chr6:33566008-33566009	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs554712351	chr6:33566009-33566010	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs77588306	chr6:33566035-33566036	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs142821066	chr6:33566120-33566121	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs556497769	chr6:33566126-33566127	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs62407596	chr6:33566129-33566130	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs210211	chr6:33566140-33566141	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs374299613	chr6:33566146-33566147	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs487762	chr6:33566158-33566159	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs553914920	chr6:33566178-33566179	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs3846859	chr6:33566210-33566211	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs3846860	chr6:33566254-33566255	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs145548091	chr6:33566288-33566289	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs59616545	chr6:33566290-33566291	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs4460206	chr6:33566318-33566319	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs182095792	chr6:33566342-33566343	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs375932119	chr6:33566353-33566354	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:109)

Disease	PMID	Source
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Melanoma	18172304	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Hepatocellular carcinoma	16750200	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
abnormal development	18461090	CNVD
Breast cancer	16397240	CNVD
Retinoblastoma	22278416	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Systemic lupus erythematosus	20877625	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Systemic lupus erythematosus	19279649	CNVD
Retinoblastoma	16790693	CNVD
Acute myocardial infarction	18032375	CNVD
Renal cell carcinoma	19150565	CNVD
Systemic lupus erythematosus	19591781	CNVD
Attention deficit hyperactivity disorder	19287146	CNVD
Autism	19287146	CNVD
Erythema nodosum in leprosy	19287146	CNVD
Henoch-schoenlein purpura	19287146	CNVD
Liver cirrhosis	19287146	CNVD
Systemic lupus erythematosus	19287146	CNVD
Autoimmune disease	19135723	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Systemic lupus erythematosus	19287147	CNVD
Osteosarcoma	16790693	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
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Myelofibrosis	22110671	CNVD
Incontinentia Pigmenti	22033527	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Encephalopathy	20692195	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Lung cancer	18438408	CNVD
Glioblastoma multiforme	21138945	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:1656 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:33558600-33567200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr6:33559000-33567200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr6:33559400-33567200	Weak transcription	Skeletal Muscle Female	skeletal muscle
4	chr6:33559600-33569800	Weak transcription	Skeletal Muscle Male	skeletal muscle
5	chr6:33561200-33567200	Weak transcription	Left Ventricle	heart
6	chr6:33561400-33565600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr6:33561400-33565600	Weak transcription	Right Ventricle	heart
8	chr6:33561400-33565600	Weak transcription	HMEC	breast
9	chr6:33561400-33567200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr6:33561400-33567200	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr6:33561400-33567200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr6:33561400-33567200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr6:33561400-33567200	Weak transcription	Esophagus	oesophagus
14	chr6:33561400-33567200	Weak transcription	Gastric	stomach
15	chr6:33561400-33567200	Weak transcription	Sigmoid Colon	Sigmoid Colon
16	chr6:33561400-33567200	Weak transcription	NH-A	brain
17	chr6:33561600-33565800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
18	chr6:33561600-33565800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
19	chr6:33561600-33565800	Weak transcription	Fetal Intestine Small	intestine
20	chr6:33561600-33567000	Weak transcription	Primary T helper cells PMA-I stimulated	--
21	chr6:33561600-33567200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
22	chr6:33561600-33567200	Weak transcription	Rectal Mucosa Donor 29	rectum
23	chr6:33561600-33567400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
24	chr6:33561600-33567400	Weak transcription	NHLF	lung
25	chr6:33561600-33570400	Weak transcription	Fetal Intestine Large	intestine
26	chr6:33563200-33565400	Weak transcription	Spleen	Spleen
27	chr6:33563400-33565600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr6:33563400-33565600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr6:33563400-33567000	Weak transcription	Muscle Satellite Cultured Cells	--
30	chr6:33563400-33567200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr6:33563400-33567200	Weak transcription	NHDF-Ad	bronchial
32	chr6:33563600-33567200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr6:33563600-33567200	Weak transcription	A549	lung
34	chr6:33564200-33565200	Enhancers	GM12878-XiMat	blood
35	chr6:33564200-33565400	Enhancers	Primary B cells from cord blood	blood
36	chr6:33564200-33566000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr6:33564200-33566200	Enhancers	Primary B cells from peripheral blood	blood
38	chr6:33564400-33567000	Weak transcription	Hela-S3	cervix
39	chr6:33564400-33567000	Weak transcription	NHEK	skin
40	chr6:33564400-33567800	Enhancers	Primary T cells fromperipheralblood	blood
41	chr6:33564600-33566000	Enhancers	HepG2	liver
42	chr6:33564600-33566200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
43	chr6:33564800-33565200	Enhancers	Primary hematopoietic stem cells short term culture	blood
44	chr6:33564800-33565200	Enhancers	HUVEC	blood vessel
45	chr6:33564800-33565600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
46	chr6:33564800-33566200	Enhancers	Primary T cells from cord blood	blood
47	chr6:33564800-33566200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
48	chr6:33564800-33566800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr6:33564800-33567400	Enhancers	Fetal Thymus	thymus
50	chr6:33565000-33565200	Enhancers	Duodenum Mucosa	Duodenum

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