Variant report

Variant	nsv886188
Chromosome Location	chr6:76411843-76469115
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:666)
CpG islands
(count:428)
Chromatin interactive
region (count:67)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:666 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:76458622-76458651	K562	blood:	n/a	n/a
2	ARID3A	chr6:76458528-76458682	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:76445315-76446019	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:76457201-76457496	HepG2	liver:	n/a	n/a
5	BACH1	chr6:76458387-76458719	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr6:76458435-76458631	K562	blood:	n/a	n/a
7	BACH1	chr6:76459213-76459671	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr6:76453741-76453966	GM12878	blood:	n/a	n/a
9	BATF	chr6:76468871-76469148	GM12878	blood:	n/a	chr6:76468983-76468994
10	BCL11A	chr6:76453638-76454028	GM12878	blood:	n/a	n/a
11	BCL11A	chr6:76453680-76454055	GM12878	blood:	n/a	n/a
12	BHLHE40	chr6:76463942-76463968	GM12878	blood:	n/a	n/a
13	BHLHE40	chr6:76463949-76464065	HepG2	liver:	n/a	n/a
14	BHLHE40	chr6:76458636-76459158	GM12878	blood:	n/a	chr6:76459001-76459017
15	BHLHE40	chr6:76458636-76459067	K562	blood:	n/a	chr6:76459001-76459017
16	BHLHE40	chr6:76452022-76452184	HepG2	liver:	n/a	chr6:76452041-76452057
17	BRCA1	chr6:76458548-76459230	Hela-S3	cervix:	n/a	n/a
18	BRCA1	chr6:76458481-76458684	H1-hESC	embryonic stem cell:	n/a	n/a
19	CBX3	chr6:76463601-76464204	HCT-116	colon:	n/a	n/a
20	CCNT2	chr6:76458398-76459210	K562	blood:	n/a	n/a
21	CEBPB	chr6:76463665-76464019	IMR90	lung:	n/a	n/a
22	CEBPB	chr6:76445676-76445920	HepG2	liver:	n/a	n/a
23	CEBPB	chr6:76465468-76465784	HepG2	liver:	n/a	chr6:76465644-76465657 chr6:76465645-76465656 chr6:76465646-76465655 chr6:76465644-76465657 chr6:76465644-76465657 chr6:76465644-76465655 chr6:76465646-76465655 chr6:76465644-76465655 chr6:76465646-76465655 chr6:76465646-76465655
24	CEBPB	chr6:76458446-76458761	IMR90	lung:	n/a	n/a
25	CEBPB	chr6:76458453-76458653	K562	blood:	n/a	n/a
26	CEBPB	chr6:76445244-76446080	HCT-116	colon:	n/a	chr6:76445651-76445662 chr6:76445652-76445664
27	CEBPB	chr6:76445228-76446111	HCT-116	colon:	n/a	chr6:76445651-76445662 chr6:76445652-76445664
28	CEBPB	chr6:76420511-76420824	IMR90	lung:	n/a	chr6:76420672-76420683
29	CEBPB	chr6:76462017-76462101	A549	lung:	n/a	chr6:76462021-76462034
30	CEBPB	chr6:76465491-76465786	IMR90	lung:	n/a	chr6:76465644-76465657 chr6:76465645-76465656 chr6:76465646-76465655 chr6:76465644-76465657 chr6:76465644-76465657 chr6:76465644-76465655 chr6:76465646-76465655 chr6:76465644-76465655 chr6:76465646-76465655 chr6:76465646-76465655
31	CEBPB	chr6:76458284-76459143	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr6:76418102-76418437	HepG2	liver:	n/a	chr6:76418257-76418268
33	CEBPB	chr6:76435609-76435850	K562	blood:	n/a	n/a
34	CEBPB	chr6:76465474-76465776	A549	lung:	n/a	chr6:76465644-76465657 chr6:76465645-76465656 chr6:76465646-76465655 chr6:76465644-76465657 chr6:76465644-76465657 chr6:76465644-76465655 chr6:76465646-76465655 chr6:76465644-76465655 chr6:76465646-76465655 chr6:76465646-76465655
35	CEBPB	chr6:76445664-76445974	MCF-7	breast:	n/a	n/a
36	CEBPB	chr6:76464790-76465019	HepG2	liver:	n/a	chr6:76464900-76464911
37	CEBPB	chr6:76420528-76420815	HepG2	liver:	n/a	chr6:76420672-76420683
38	CEBPB	chr6:76458311-76458775	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr6:76458442-76458796	HepG2	liver:	n/a	n/a
40	CEBPB	chr6:76445756-76445832	A549	lung:	n/a	n/a
41	CEBPB	chr6:76465464-76465810	Hela-S3	cervix:	n/a	chr6:76465644-76465657 chr6:76465645-76465656 chr6:76465646-76465655 chr6:76465644-76465657 chr6:76465644-76465657 chr6:76465644-76465655 chr6:76465646-76465655 chr6:76465644-76465655 chr6:76465646-76465655 chr6:76465646-76465655
42	CEBPD	chr6:76458657-76459159	HepG2	liver:	n/a	n/a
43	CHD1	chr6:76459425-76459893	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD1	chr6:76459472-76459797	GM12878	blood:	n/a	n/a
45	CHD1	chr6:76458458-76458771	H1-hESC	embryonic stem cell:	n/a	chr6:76458550-76458560
46	CHD1	chr6:76458044-76459218	GM12878	blood:	n/a	chr6:76458550-76458560
47	CHD1	chr6:76459058-76459131	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD2	chr6:76458348-76459225	GM12878	blood:	n/a	chr6:76458550-76458560
49	CHD2	chr6:76458470-76458675	K562	blood:	n/a	chr6:76458550-76458560
50	CHD2	chr6:76458450-76459267	H1-hESC	embryonic stem cell:	n/a	chr6:76458550-76458560

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:76458633-76458683	HUVEC	blood vessel:	n/a
2	chr6:76458633-76458683	HUVEC	blood vessel:	n/a
3	chr6:76458005-76458055	NHDF-neo	bronchial:	n/a
4	chr6:76458633-76458683	HRPEpiC	eye:	n/a
5	chr6:76456187-76456237	MCF-7	breast:	n/a
6	chr6:76456187-76456237	HNPCEpiC	eye:	n/a
7	chr6:76456187-76456237	BJ	skin:	n/a
8	chr6:76425457-76425507	AG04450	lung:	fetal
9	chr6:76461321-76461371	K562	blood:	n/a
10	chr6:76458005-76458055	PFSK-1	brain:	n/a
11	chr6:76425457-76425507	GM12878	blood:	n/a
12	chr6:76458633-76458683	GM19239	blood:	n/a
13	chr6:76459077-76459127	HUVEC	blood vessel:	n/a
14	chr6:76458005-76458055	H1-hESC	embryonic stem cell:	embryo
15	chr6:76459077-76459127	HL-60	blood:	n/a
16	chr6:76425457-76425507	SK-N-SH	brain:	n/a
17	chr6:76425457-76425507	HepG2	liver:	n/a
18	chr6:76456187-76456237	HepG2	liver:	n/a
19	chr6:76458005-76458055	HRPEpiC	eye:	n/a
20	chr6:76456187-76456237	ovcar-3	ovarian:	n/a
21	chr6:76425457-76425507	CMK	blood:	n/a
22	chr6:76458005-76458055	AoSMC	blood vessel:	n/a
23	chr6:76456187-76456237	SK-N-MC	brain:	n/a
24	chr6:76458005-76458055	MCF-7	breast:	n/a
25	chr6:76458633-76458683	SKMC	muscle:	n/a
26	chr6:76461321-76461371	AG04449	skin:	fetal
27	chr6:76461321-76461371	HEEpiC	esophagus:	n/a
28	chr6:76458633-76458683	HIPEpiC	eye:	n/a
29	chr6:76459077-76459127	AoSMC	blood vessel:	n/a
30	chr6:76461321-76461371	Jurkat	blood:	n/a
31	chr6:76425457-76425507	HL-60	blood:	n/a
32	chr6:76456187-76456237	Hepatocyte	liver:	n/a
33	chr6:76456187-76456237	ECC-1	luminal epithelium:	n/a
34	chr6:76459077-76459127	ECC-1	luminal epithelium:	n/a
35	chr6:76459077-76459127	IMR90	lung:	fetal
36	chr6:76458005-76458055	SKMC	muscle:	n/a
37	chr6:76459511-76459561	HL-60	blood:	n/a
38	chr6:76456187-76456237	AG09309	skin:	n/a
39	chr6:76459511-76459561	HMEC	breast:	n/a
40	chr6:76459511-76459561	AoSMC	blood vessel:	n/a
41	chr6:76458633-76458683	SK-N-SH	brain:	n/a
42	chr6:76459077-76459127	PANC-1	pancreas:	n/a
43	chr6:76425457-76425507	NT2-D1	testis:	n/a
44	chr6:76458633-76458683	Jurkat	blood:	n/a
45	chr6:76459077-76459127	SK-N-MC	brain:	n/a
46	chr6:76459077-76459127	MCF-7	breast:	n/a
47	chr6:76456187-76456237	HEK293	kidney:	embryo
48	chr6:76458633-76458683	U87	brain:	n/a
49	chr6:76458005-76458055	HepG2	liver:	n/a
50	chr6:76458005-76458055	HCT-116	colon:	n/a

(count:67 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:76443216..76445538-chr6:76460929..76463884,2	K562	blood:
2	chr6:76406647..76409621-chr6:76410785..76413589,2	K562	blood:
3	chr6:76443894..76445853-chr6:76451155..76454793,3	MCF-7	breast:
4	chr6:76316195..76318634-chr6:76459170..76461001,2	K562	blood:
5	chr6:76457754..76460582-chr6:76467683..76471676,6	MCF-7	breast:
6	chr6:76467679..76469997-chr6:76472807..76474955,2	K562	blood:
7	chr6:76461153..76463947-chr6:76466842..76469998,3	MCF-7	breast:
8	chr6:76441614..76445337-chr6:76457792..76459831,5	MCF-7	breast:
9	chr6:76458966..76460939-chr6:76574214..76577179,2	MCF-7	breast:
10	chr6:76424657..76427289-chr6:76428050..76430901,3	MCF-7	breast:
11	chr6:76424414..76426953-chr6:76430333..76433018,2	MCF-7	breast:
12	chr6:76426476..76430048-chr6:76457436..76461171,5	MCF-7	breast:
13	chr6:76423793..76426485-chr6:76434093..76435596,2	K562	blood:
14	chr6:76424414..76426953-chr6:76430333..76433018,2	MCF-7	breast:
15	chr6:76420291..76423663-chr6:76455456..76460338,5	MCF-7	breast:
16	chr6:76426836..76429906-chr6:76458673..76460595,3	MCF-7	breast:
17	chr6:76457614..76459414-chr6:76469003..76470756,2	K562	blood:
18	chr6:76465017..76467292-chr6:76472497..76474825,2	K562	blood:
19	chr6:76423467..76426296-chr6:76461021..76463732,3	MCF-7	breast:
20	chr3:141205080..141206779-chr6:76458156..76460847,2	MCF-7	breast:
21	chr6:76458851..76461812-chr6:76463826..76465926,2	K562	blood:
22	chr6:76459743..76462264-chr6:76558072..76560658,3	MCF-7	breast:
23	chr6:76465841..76467549-chr6:76494669..76496179,2	MCF-7	breast:
24	chr6:76416198..76418365-chr6:76457940..76460718,3	MCF-7	breast:
25	chr6:76311833..76313694-chr6:76456932..76459481,3	MCF-7	breast:
26	chr2:233562031..233562988-chr6:76458771..76459462,2	Hela-S3	cervix:
27	chr6:75982004..75984074-chr6:76410920..76413580,2	K562	blood:
28	chr6:76450359..76452041-chr6:76457600..76459670,2	MCF-7	breast:
29	chr6:76463940..76466517-chr6:76472497..76474287,2	K562	blood:
30	chr6:76416294..76419277-chr6:76420477..76423022,2	K562	blood:
31	chr6:76405218..76407618-chr6:76430939..76433858,2	MCF-7	breast:
32	chr6:76402073..76403999-chr6:76420565..76422699,2	MCF-7	breast:
33	chr6:76413657..76415200-chr6:76420816..76423209,2	MCF-7	breast:
34	chr6:76413657..76415200-chr6:76420816..76423209,2	MCF-7	breast:
35	chr6:76456068..76458008-chr6:76564755..76567247,2	MCF-7	breast:
36	chr6:76446062..76448644-chr6:76456702..76459457,3	MCF-7	breast:
37	chr6:76463962..76466709-chr6:76471388..76473486,2	MCF-7	breast:
38	chr6:76416294..76419277-chr6:76420477..76423022,2	K562	blood:
39	chr6:76467657..76469847-chr6:76559756..76561654,2	MCF-7	breast:
40	chr6:76423793..76426485-chr6:76434093..76435596,2	K562	blood:
41	chr6:76443216..76445538-chr6:76460929..76463884,2	K562	blood:
42	chr6:76461303..76463860-chr6:76468925..76471220,2	K562	blood:
43	chr6:76457060..76461197-chr6:76473704..76478813,6	MCF-7	breast:
44	chr6:76443894..76445853-chr6:76451155..76454793,3	MCF-7	breast:
45	chr6:76458766..76460644-chr6:76463670..76465363,2	MCF-7	breast:
46	chr6:76424657..76427289-chr6:76428050..76430901,3	MCF-7	breast:
47	chr6:76461468..76463754-chr6:76469518..76472253,2	MCF-7	breast:
48	chr6:76408144..76410485-chr6:76410972..76412755,2	MCF-7	breast:
49	chr6:76445351..76447592-chr6:76454801..76459037,4	MCF-7	breast:
50	chr6:76456505..76458923-chr6:76460845..76462733,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SENP6-4	chr6:76433669-76434665	NONHSAT113631
2	lnc-SENP6-5	chr6:76434955-76435356	NONHSAT113632

No data

Variant related genes	Relation type
MYO6	TF binding region
MYO6	CpG island
ENSG00000112701	chromatin interactions
ENSG00000112697	chromatin interactions
ENSG00000166012	chromatin interactions
ENSG00000239132	chromatin interactions
ENSG00000217488	chromatin interactions
ENSG00000204120	chromatin interactions
ENSG00000196586	chromatin interactions
ENSG00000124596	chromatin interactions
ENSG00000155903	chromatin interactions
ENSG00000143971	chromatin interactions
ENSG00000252156	chromatin interactions
ENSG00000001167	chromatin interactions
ENSG00000223169	chromatin interactions
ENSG00000182919	chromatin interactions

Extended variants
information (count: 2001 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:2001 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9343317	chr6:76411843-76411844	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs188547564	chr6:76411900-76411901	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs543012610	chr6:76411910-76411911	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs200531593	chr6:76411935-76411936	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs76507265	chr6:76411948-76411949	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs181384371	chr6:76412003-76412004	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs118094425	chr6:76412075-76412076	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs146736382	chr6:76412172-76412173	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs185921391	chr6:76412177-76412178	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs527809755	chr6:76412213-76412214	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs190789619	chr6:76412214-76412215	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs140329129	chr6:76412229-76412230	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs537382911	chr6:76412275-76412276	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs201673325	chr6:76412387-76412388	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs370244586	chr6:76412394-76412395	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs377539784	chr6:76412445-76412446	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs201057204	chr6:76412455-76412456	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs375569038	chr6:76412473-76412474	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs201398729	chr6:76412494-76412495	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs34045941	chr6:76412531-76412532	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs375397460	chr6:76412567-76412568	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs568748626	chr6:76412572-76412573	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs183792140	chr6:76412588-76412589	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs371776397	chr6:76412617-76412618	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs74455858	chr6:76412653-76412654	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs373788740	chr6:76412669-76412670	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs367965753	chr6:76412671-76412672	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs146566386	chr6:76412698-76412699	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs187628440	chr6:76412746-76412747	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs533274763	chr6:76412756-76412757	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs369405641	chr6:76412760-76412761	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs149140428	chr6:76412762-76412763	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs200513593	chr6:76412776-76412777	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs576009193	chr6:76412824-76412825	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs376716656	chr6:76412832-76412833	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs201827129	chr6:76412838-76412839	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs543427207	chr6:76412853-76412854	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs561491514	chr6:76412871-76412872	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs529224263	chr6:76412884-76412885	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs143212068	chr6:76412896-76412897	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs148297485	chr6:76412898-76412899	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs532953549	chr6:76412942-76412943	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs190756161	chr6:76412959-76412960	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs564623876	chr6:76412979-76412980	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs551739039	chr6:76412988-76412989	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs11754663	chr6:76412992-76412993	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs550180671	chr6:76413001-76413002	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs199819513	chr6:76413009-76413010	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs568340475	chr6:76413015-76413016	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs77922692	chr6:76413017-76413018	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:98)

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
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	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
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Systemic lupus erythematosus	17503323	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Lung cancer	18438408	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
Ependymoma	16718352	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
Prostate cancer	16573809	CNVD
Breast cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Follicular lymphoma	17699855	CNVD
Breast cancer	17133270	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	CNVD
Developmental delay	21147756	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Salivary gland tumor	18059337	CNVD
Lung cancer	16773561	CNVD
Glioblastoma multiforme	22286061	CNVD
Urothelial cell carcinoma	18451213	CNVD
Prostate cancer	16461572	CNVD
Mental retardation	21045960	CNVD
Obesity	21045960	CNVD
learning difficulties	21045960	CNVD
Prostate cancer	17245344	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1316 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:76382000-76422800	Weak transcription	Stomach Mucosa	stomach
2	chr6:76391400-76417200	Weak transcription	Gastric	stomach
3	chr6:76391400-76421200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr6:76391400-76426600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr6:76391600-76419200	Weak transcription	Right Ventricle	heart
6	chr6:76391600-76427200	Weak transcription	Small Intestine	intestine
7	chr6:76392000-76412200	Weak transcription	HepG2	liver
8	chr6:76392000-76412400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
9	chr6:76392000-76421400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
10	chr6:76392000-76423400	Weak transcription	NHEK	skin
11	chr6:76392000-76423800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
12	chr6:76392200-76420400	Weak transcription	Fetal Heart	heart
13	chr6:76392200-76421000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
14	chr6:76392200-76426800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
15	chr6:76395200-76420200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr6:76396800-76414600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr6:76396800-76414600	Strong transcription	Duodenum Mucosa	Duodenum
18	chr6:76396800-76414800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr6:76397000-76413400	Strong transcription	Fetal Thymus	thymus
20	chr6:76397200-76415800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
21	chr6:76397200-76418000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr6:76397400-76413600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr6:76397400-76414000	Strong transcription	Dnd41	blood
24	chr6:76397400-76415000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr6:76397400-76430800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr6:76398000-76421000	Weak transcription	K562	blood
27	chr6:76398000-76428200	Weak transcription	Colonic Mucosa	Colon
28	chr6:76398200-76417200	Weak transcription	Spleen	Spleen
29	chr6:76398400-76425400	Weak transcription	Pancreas	Pancrea
30	chr6:76399800-76426200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr6:76400000-76412800	Weak transcription	Aorta	Aorta
32	chr6:76400000-76413800	Weak transcription	Rectal Smooth Muscle	rectum
33	chr6:76401600-76413600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr6:76401600-76426400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
35	chr6:76402000-76414200	Strong transcription	Primary monocytes fromperipheralblood	blood
36	chr6:76402000-76414200	Strong transcription	Monocytes-CD14+_RO01746	blood
37	chr6:76402200-76414200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
38	chr6:76402200-76415000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr6:76402200-76425400	Strong transcription	Fetal Intestine Large	intestine
40	chr6:76402600-76413800	Strong transcription	HUES48 Cell Line	embryonic stem cell
41	chr6:76402800-76417200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr6:76403400-76414400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr6:76404800-76415200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr6:76405200-76414800	Strong transcription	Fetal Muscle Trunk	muscle
45	chr6:76405400-76414800	Strong transcription	Primary neutrophils fromperipheralblood	blood
46	chr6:76405600-76413400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
47	chr6:76405600-76414000	Strong transcription	Placenta	Placenta
48	chr6:76405600-76414600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr6:76405600-76415000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr6:76406200-76414800	Strong transcription	Fetal Muscle Leg	muscle

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