Variant report

Variant	nsv602909
Chromosome Location	chr6:35356640-35423489
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1757)
CpG islands
(count:1101)
Chromatin interactive
region (count:123)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1757 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:35396271-35396729	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:35370124-35370816	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:35361195-35361536	K562	blood:	n/a	n/a
4	ARID3A	chr6:35382989-35383735	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:35420069-35420086	K562	blood:	n/a	n/a
6	ARID3A	chr6:35417234-35417536	HepG2	liver:	n/a	n/a
7	ATF2	chr6:35369816-35370255	GM12878	blood:	n/a	n/a
8	ATF3	chr6:35407157-35407351	K562	blood:	n/a	n/a
9	ATF3	chr6:35362109-35362420	K562	blood:	n/a	n/a
10	BACH1	chr6:35361244-35361491	K562	blood:	n/a	n/a
11	BATF	chr6:35369898-35370257	GM12878	blood:	n/a	n/a
12	BHLHE40	chr6:35419895-35420465	GM12878	blood:	n/a	chr6:35420093-35420109
13	BHLHE40	chr6:35417246-35417608	K562	blood:	n/a	n/a
14	BHLHE40	chr6:35364778-35365019	K562	blood:	n/a	n/a
15	BHLHE40	chr6:35382929-35383603	HepG2	liver:	n/a	n/a
16	BHLHE40	chr6:35420869-35421061	GM12878	blood:	n/a	n/a
17	BHLHE40	chr6:35383074-35383353	K562	blood:	n/a	n/a
18	BHLHE40	chr6:35419901-35420412	HepG2	liver:	n/a	chr6:35420093-35420109
19	BHLHE40	chr6:35417248-35417555	HepG2	liver:	n/a	n/a
20	BHLHE40	chr6:35377200-35377221	K562	blood:	n/a	n/a
21	BHLHE40	chr6:35396260-35396788	HepG2	liver:	n/a	n/a
22	BHLHE40	chr6:35369900-35370307	GM12878	blood:	n/a	n/a
23	BHLHE40	chr6:35419768-35421380	K562	blood:	n/a	chr6:35420093-35420109
24	BHLHE40	chr6:35361595-35362430	K562	blood:	n/a	n/a
25	BHLHE40	chr6:35374200-35374326	K562	blood:	n/a	n/a
26	BRCA1	chr6:35396384-35396854	HepG2	liver:	n/a	n/a
27	BRCA1	chr6:35417636-35417652	HepG2	liver:	n/a	n/a
28	BRCA1	chr6:35417300-35417499	Hela-S3	cervix:	n/a	n/a
29	BRCA1	chr6:35419947-35420433	Hela-S3	cervix:	n/a	n/a
30	BRCA1	chr6:35382778-35383456	HepG2	liver:	n/a	n/a
31	BRCA1	chr6:35420098-35420268	HepG2	liver:	n/a	n/a
32	CBX3	chr6:35396865-35397783	K562	blood:	n/a	n/a
33	CBX3	chr6:35420512-35420895	K562	blood:	n/a	n/a
34	CBX3	chr6:35397213-35397703	K562	blood:	n/a	n/a
35	CBX3	chr6:35419860-35420442	K562	blood:	n/a	n/a
36	CCNT2	chr6:35361194-35361434	K562	blood:	n/a	n/a
37	CCNT2	chr6:35419875-35420761	K562	blood:	n/a	chr6:35419910-35419919
38	CCNT2	chr6:35421067-35421311	K562	blood:	n/a	n/a
39	CCNT2	chr6:35387389-35387589	K562	blood:	n/a	n/a
40	CCNT2	chr6:35364796-35364928	K562	blood:	n/a	n/a
41	CEBPB	chr6:35370377-35370639	HepG2	liver:	n/a	n/a
42	CEBPB	chr6:35422379-35422401	K562	blood:	n/a	n/a
43	CEBPB	chr6:35422315-35422546	H1-hESC	embryonic stem cell:	n/a	chr6:35422393-35422404
44	CEBPB	chr6:35377013-35377434	K562	blood:	n/a	chr6:35377232-35377243
45	CEBPB	chr6:35421739-35422055	IMR90	lung:	n/a	chr6:35421896-35421907
46	CEBPB	chr6:35387162-35387462	HepG2	liver:	n/a	chr6:35387274-35387285
47	CEBPB	chr6:35421700-35422095	ECC-1	luminal epithelium:	n/a	chr6:35421896-35421907
48	CEBPB	chr6:35383002-35383525	HepG2	liver:	n/a	n/a
49	CEBPB	chr6:35417038-35417355	HepG2	liver:	n/a	chr6:35417178-35417189
50	CEBPB	chr6:35421848-35422000	H1-hESC	embryonic stem cell:	n/a	chr6:35421896-35421907

(count:1101 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:35418721-35418771	NT2-D1	testis:	n/a
2	chr6:35395209-35395259	U87	brain:	n/a
3	chr6:35419793-35419843	HepG2	liver:	n/a
4	chr6:35418721-35418771	NT2-D1	testis:	n/a
5	chr6:35395209-35395259	U87	brain:	n/a
6	chr6:35419793-35419843	HepG2	liver:	n/a
7	chr6:35419793-35419843	K562	blood:	n/a
8	chr6:35392736-35392786	HCF	heart:	n/a
9	chr6:35392246-35392296	GM12878	blood:	n/a
10	chr6:35392736-35392786	CMK	blood:	n/a
11	chr6:35387204-35387254	NT2-D1	testis:	n/a
12	chr6:35392381-35392431	HepG2	liver:	n/a
13	chr6:35422526-35422576	HEK293	kidney:	embryo
14	chr6:35403738-35403788	K562	blood:	n/a
15	chr6:35418721-35418771	CMK	blood:	n/a
16	chr6:35417568-35417618	BJ	skin:	n/a
17	chr6:35392381-35392431	IMR90	lung:	fetal
18	chr6:35370123-35370173	HRCEpiC	kidney:	n/a
19	chr6:35420754-35420804	HCT-116	colon:	n/a
20	chr6:35419979-35420029	NH-A	brain:	n/a
21	chr6:35419793-35419843	SK-N-SH	brain:	n/a
22	chr6:35392381-35392431	NT2-D1	testis:	n/a
23	chr6:35403738-35403788	PFSK-1	brain:	n/a
24	chr6:35387204-35387254	HEEpiC	esophagus:	n/a
25	chr6:35392306-35392356	HepG2	liver:	n/a
26	chr6:35392306-35392356	HIPEpiC	eye:	n/a
27	chr6:35422526-35422576	Hela-S3	cervix:	n/a
28	chr6:35392306-35392356	A549	lung:	n/a
29	chr6:35418721-35418771	AoSMC	blood vessel:	n/a
30	chr6:35420303-35420353	HCPEpiC	choroid plexus:	n/a
31	chr6:35387204-35387254	NB4	blood:	n/a
32	chr6:35403738-35403788	HMEC	breast:	n/a
33	chr6:35395209-35395259	MCF-7	breast:	n/a
34	chr6:35370123-35370173	HRPEpiC	eye:	n/a
35	chr6:35360715-35360765	HCT-116	colon:	n/a
36	chr6:35392306-35392356	AoSMC	blood vessel:	n/a
37	chr6:35392736-35392786	IMR90	lung:	fetal
38	chr6:35395209-35395259	AG09309	skin:	n/a
39	chr6:35418721-35418771	GM12891	blood:	n/a
40	chr6:35422526-35422576	ProgFib	skin:	n/a
41	chr6:35395209-35395259	RPTEC	kidney:	n/a
42	chr6:35395209-35395259	GM12878	blood:	n/a
43	chr6:35392306-35392356	BE2_C	brain:	n/a
44	chr6:35420303-35420353	MCF10A-Er-Src	breast:	n/a
45	chr6:35370123-35370173	H1-hESC	embryonic stem cell:	embryo
46	chr6:35392381-35392431	HCM	heart:	n/a
47	chr6:35419997-35420047	K562	blood:	n/a
48	chr6:35419979-35420029	SKMC	muscle:	n/a
49	chr6:35370123-35370173	HIPEpiC	eye:	n/a
50	chr6:35417568-35417618	HCT-116	colon:	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr6:35405229..35407792-chr6:35409420..35411171,2	MCF-7	breast:
2	chr6:35386381..35389895-chr6:35435947..35439155,3	K562	blood:
3	chr6:35368369..35371007-chr6:35374165..35376691,3	K562	blood:
4	chr6:35309722..35310228-chr6:35360820..35361514,2	K562	blood:
5	chr6:35357119..35359280-chr6:35381756..35383497,2	MCF-7	breast:
6	chr6:35264934..35265718-chr6:35382748..35383526,3	K562	blood:
7	chr6:35329516..35331357-chr6:35414817..35417634,2	MCF-7	breast:
8	chr6:35390023..35392138-chr6:35401114..35403193,2	K562	blood:
9	chr6:35364935..35367619-chr6:35369623..35372118,3	K562	blood:
10	chr6:35415085..35416689-chr6:35421187..35424185,2	K562	blood:
11	chr6:35401564..35403389-chr6:35434322..35438039,3	K562	blood:
12	chr6:35313010..35315101-chr6:35358696..35360366,2	MCF-7	breast:
13	chr6:35333771..35336611-chr6:35358813..35361070,2	MCF-7	breast:
14	chr6:35265057..35265957-chr6:35419424..35420709,3	K562	blood:
15	chr6:35253202..35255574-chr6:35420736..35422300,2	MCF-7	breast:
16	chr6:35328136..35331103-chr6:35385311..35387478,2	MCF-7	breast:
17	chr6:35415017..35416617-chr6:35436362..35437925,2	MCF-7	breast:
18	chr6:35258451..35260687-chr6:35421514..35424141,3	MCF-7	breast:
19	chr6:35382683..35384184-chr6:35386582..35388142,2	K562	blood:
20	chr6:35364744..35367159-chr6:35371168..35373202,2	MCF-7	breast:
21	chr6:35374932..35377738-chr6:35417292..35420237,2	K562	blood:
22	chr6:35262981..35267829-chr6:35418945..35424124,7	K562	blood:
23	chr6:35327509..35329101-chr6:35368128..35370568,2	K562	blood:
24	chr6:35387457..35387973-chr6:35417155..35417800,2	MCF-7	breast:
25	chr1:35658635..35659143-chr6:35386008..35386508,2	Hela-S3	cervix:
26	chr6:35309118..35313462-chr6:35418133..35422102,7	MCF-7	breast:
27	chr6:35357119..35359280-chr6:35381756..35383497,2	MCF-7	breast:
28	chr6:35352372..35354969-chr6:35356317..35359445,3	K562	blood:
29	chr6:35310264..35312853-chr6:35403598..35406051,2	K562	blood:
30	chr6:35395055..35396641-chr6:35399730..35402095,2	MCF-7	breast:
31	chr6:35266653..35267496-chr6:35416841..35417464,3	K562	blood:
32	chr6:35384923..35387386-chr6:35435041..35437575,2	MCF-7	breast:
33	chr6:35413046..35416291-chr6:35417429..35420462,4	K562	blood:
34	chr6:35395055..35396641-chr6:35399730..35402095,2	MCF-7	breast:
35	chr6:35386287..35387905-chr6:35391814..35393487,2	MCF-7	breast:
36	chr6:35348461..35351306-chr6:35356739..35359433,2	MCF-7	breast:
37	chr6:35390370..35392093-chr6:35395033..35397221,2	K562	blood:
38	chr6:35226026..35228002-chr6:35394504..35397292,2	K562	blood:
39	chr6:35355898..35357856-chr6:35435877..35438604,2	MCF-7	breast:
40	chr6:35327015..35329027-chr6:35357004..35359462,2	K562	blood:
41	chr6:35265080..35265878-chr6:35403707..35404212,2	MCF-7	breast:
42	chr6:35364935..35367587-chr6:35369436..35372009,4	K562	blood:
43	chr6:35265049..35266094-chr6:35416870..35417859,12	K562	blood:
44	chr6:35385294..35388987-chr6:35389022..35393579,4	K562	blood:
45	chr6:35309852..35312289-chr6:35417832..35421264,4	K562	blood:
46	chr6:35364744..35367159-chr6:35371168..35373202,2	MCF-7	breast:
47	chr6:35299795..35300338-chr6:35417088..35417923,2	MCF-7	breast:
48	chr6:35417496..35419930-chr6:35463187..35465266,3	MCF-7	breast:
49	chr6:35225451..35228151-chr6:35375236..35377988,2	K562	blood:
50	chr6:35369456..35371995-chr6:35391240..35394220,2	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PPARD-2	chr6:35399993-35400219	NONHSAT112181
2	lnc-PPARD-1	chr6:35397970-35398533	NONHSAT112180
3	lnc-FANCE-1	chr6:35394662-35394997	NONHSAT112179

No data

Variant related genes	Relation type
ENSG00000227154	TF binding region
FANCE	TF binding region
ENSG00000227154	CpG island
FANCE	CpG island
ENSG00000132694	chromatin interactions
ENSG00000204568	chromatin interactions
ENSG00000227154	chromatin interactions
ENSG00000112039	chromatin interactions
ENSG00000198755	chromatin interactions
ENSG00000065029	chromatin interactions
ENSG00000112033	chromatin interactions
ENSG00000023892	chromatin interactions
ENSG00000007866	chromatin interactions
ENSG00000116560	chromatin interactions

Extended variants
information (count: 2802 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:2802 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9658100	chr6:35356640-35356641	Weak transcription Flanking Active TSS Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs532908169	chr6:35356642-35356643	Weak transcription Flanking Active TSS Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs60514539	chr6:35356662-35356663	Weak transcription Flanking Active TSS Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs369518188	chr6:35356679-35356680	Weak transcription Flanking Active TSS Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs566380837	chr6:35356713-35356714	Weak transcription Flanking Active TSS Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs374231900	chr6:35356753-35356754	Weak transcription Flanking Active TSS Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs548855221	chr6:35356765-35356766	Weak transcription Flanking Active TSS Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs9658101	chr6:35356783-35356784	Weak transcription Flanking Active TSS Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs77970072	chr6:35356786-35356787	Weak transcription Flanking Active TSS Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs79964971	chr6:35356788-35356789	Weak transcription Flanking Active TSS Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs535681332	chr6:35356790-35356791	Weak transcription Flanking Active TSS Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs188573647	chr6:35356800-35356801	Weak transcription Flanking Active TSS Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs181035061	chr6:35356850-35356851	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs9658102	chr6:35356854-35356855	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs543688346	chr6:35356959-35356960	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs369657461	chr6:35356971-35356972	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs573270451	chr6:35357066-35357067	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs138335713	chr6:35357092-35357093	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs9296150	chr6:35357157-35357158	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs143278384	chr6:35357174-35357175	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs573737837	chr6:35357226-35357227	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs9658103	chr6:35357249-35357250	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs562742652	chr6:35357277-35357278	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs578008926	chr6:35357333-35357334	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs545840697	chr6:35357335-35357336	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs545352004	chr6:35357341-35357342	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs560091859	chr6:35357379-35357380	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs141409312	chr6:35357380-35357381	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs549024565	chr6:35357382-35357383	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs560823540	chr6:35357385-35357386	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs529419028	chr6:35357410-35357411	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs550779609	chr6:35357411-35357412	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs569143150	chr6:35357484-35357485	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs185250652	chr6:35357500-35357501	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs576240235	chr6:35357539-35357540	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs79521065	chr6:35357541-35357542	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs374146959	chr6:35357593-35357594	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs551834371	chr6:35357603-35357604	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs566849028	chr6:35357645-35357646	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs150917267	chr6:35357651-35357652	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs9658105	chr6:35357674-35357675	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs113364787	chr6:35357675-35357676	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs542312481	chr6:35357677-35357678	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs3798343	chr6:35357693-35357694	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs144000604	chr6:35357697-35357698	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs9658106	chr6:35357725-35357726	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs372785779	chr6:35357728-35357729	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs577960723	chr6:35357734-35357735	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs190103236	chr6:35357736-35357737	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs9658107	chr6:35357785-35357786	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:105)

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
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
Acute lymphoblastic leukemia	22237106	CNVD
Lung cancer	18438408	CNVD
Glioblastoma multiforme	21138945	CNVD
Breast cancer	21364760	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:3084 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:35338400-35378400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr6:35338600-35359400	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr6:35339600-35357800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr6:35340000-35357600	Weak transcription	Primary T helper cells fromperipheralblood	blood
5	chr6:35340600-35359400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
6	chr6:35344400-35358000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
7	chr6:35345600-35378400	Weak transcription	Aorta	Aorta
8	chr6:35346200-35359200	Weak transcription	Duodenum Smooth Muscle	Duodenum
9	chr6:35346200-35359800	Weak transcription	Stomach Smooth Muscle	stomach
10	chr6:35347400-35357600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
11	chr6:35347600-35359200	Weak transcription	Brain Angular Gyrus	brain
12	chr6:35347600-35359200	Weak transcription	Brain Substantia Nigra	brain
13	chr6:35349600-35359200	Weak transcription	Gastric	stomach
14	chr6:35350200-35358000	Weak transcription	Adipose Nuclei	Adipose
15	chr6:35350200-35359400	Weak transcription	Liver	Liver
16	chr6:35350400-35358400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
17	chr6:35351000-35357800	Weak transcription	Right Atrium	heart
18	chr6:35351000-35359000	Weak transcription	Primary T cells from cord blood	blood
19	chr6:35351000-35359200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr6:35351000-35359400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr6:35351000-35360200	Weak transcription	Primary B cells from peripheral blood	blood
22	chr6:35351000-35360800	Weak transcription	Primary B cells from cord blood	blood
23	chr6:35351000-35363400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr6:35351200-35357600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
25	chr6:35351200-35357800	Weak transcription	Dnd41	blood
26	chr6:35351200-35359200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
27	chr6:35351200-35359400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
28	chr6:35351200-35359600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr6:35353600-35358000	Enhancers	Placenta	Placenta
30	chr6:35353800-35359000	Weak transcription	Brain Inferior Temporal Lobe	brain
31	chr6:35354000-35357600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr6:35354000-35357600	Weak transcription	HMEC	breast
33	chr6:35354000-35357800	Weak transcription	Skeletal Muscle Female	skeletal muscle
34	chr6:35354000-35358400	Weak transcription	Primary T cells fromperipheralblood	blood
35	chr6:35354000-35358400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
36	chr6:35354000-35358600	Weak transcription	NHLF	lung
37	chr6:35354000-35359000	Weak transcription	Skeletal Muscle Male	skeletal muscle
38	chr6:35354000-35359200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr6:35354000-35359200	Weak transcription	Brain Cingulate Gyrus	brain
40	chr6:35354000-35359200	Weak transcription	Fetal Lung	lung
41	chr6:35354000-35359200	Weak transcription	HSMMtube	muscle
42	chr6:35354000-35359400	Weak transcription	Left Ventricle	heart
43	chr6:35354000-35359600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
44	chr6:35354000-35359600	Weak transcription	Fetal Heart	heart
45	chr6:35354000-35359600	Weak transcription	Psoas Muscle	Psoas
46	chr6:35354000-35359800	Weak transcription	Fetal Stomach	stomach
47	chr6:35354000-35360800	Weak transcription	Fetal Thymus	thymus
48	chr6:35354000-35372400	Weak transcription	Cortex derived primary cultured neurospheres	brain
49	chr6:35354200-35359200	Weak transcription	NHDF-Ad	bronchial
50	chr6:35354400-35357600	Weak transcription	Muscle Satellite Cultured Cells	--

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