Variant report

Variant	nsv871312
Chromosome Location	chr1:46196813-46353332
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2579)
CpG islands
(count:1469)
Chromatin interactive
region (count:203)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2579 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:46218650-46218651	K562	blood:	n/a	n/a
2	ARID3A	chr1:46275452-46275617	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:46268499-46269278	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:46350455-46350607	K562	blood:	n/a	n/a
5	ARID3A	chr1:46334608-46334873	HepG2	liver:	n/a	n/a
6	ARID3A	chr1:46216049-46216745	K562	blood:	n/a	n/a
7	ARID3A	chr1:46347288-46347573	HepG2	liver:	n/a	n/a
8	ARID3A	chr1:46288374-46288666	HepG2	liver:	n/a	n/a
9	ARID3A	chr1:46216078-46216749	HepG2	liver:	n/a	n/a
10	ARID3A	chr1:46336921-46338303	HepG2	liver:	n/a	n/a
11	ARID3A	chr1:46219186-46219590	K562	blood:	n/a	n/a
12	ARID3A	chr1:46350498-46350690	HepG2	liver:	n/a	n/a
13	ARID3A	chr1:46268405-46269160	K562	blood:	n/a	n/a
14	ARID3A	chr1:46212733-46212803	K562	blood:	n/a	n/a
15	ARID3A	chr1:46217849-46218734	HepG2	liver:	n/a	n/a
16	ATF1	chr1:46241660-46241827	K562	blood:	n/a	n/a
17	ATF1	chr1:46219179-46219477	K562	blood:	n/a	n/a
18	ATF1	chr1:46215975-46216656	K562	blood:	n/a	n/a
19	ATF1	chr1:46252905-46252920	K562	blood:	n/a	n/a
20	ATF1	chr1:46268403-46269065	K562	blood:	n/a	n/a
21	ATF1	chr1:46309326-46309534	K562	blood:	n/a	n/a
22	ATF2	chr1:46216159-46216812	H1-hESC	embryonic stem cell:	n/a	n/a
23	ATF2	chr1:46268444-46268793	H1-hESC	embryonic stem cell:	n/a	n/a
24	ATF2	chr1:46268393-46268945	GM12878	blood:	n/a	n/a
25	ATF2	chr1:46306272-46306830	GM12878	blood:	n/a	n/a
26	ATF2	chr1:46268462-46268881	GM12878	blood:	n/a	n/a
27	ATF2	chr1:46216149-46216697	GM12878	blood:	n/a	n/a
28	ATF2	chr1:46215714-46216734	GM12878	blood:	n/a	n/a
29	ATF2	chr1:46216108-46216795	H1-hESC	embryonic stem cell:	n/a	n/a
30	ATF2	chr1:46268428-46268979	H1-hESC	embryonic stem cell:	n/a	n/a
31	ATF3	chr1:46268279-46268864	K562	blood:	n/a	n/a
32	ATF3	chr1:46215909-46216646	K562	blood:	n/a	n/a
33	ATF3	chr1:46216207-46216693	A549	lung:	n/a	n/a
34	ATF3	chr1:46337783-46338146	A549	lung:	n/a	n/a
35	ATF3	chr1:46268962-46269408	K562	blood:	n/a	n/a
36	BACH1	chr1:46269744-46269925	H1-hESC	embryonic stem cell:	n/a	n/a
37	BACH1	chr1:46232313-46232331	K562	blood:	n/a	n/a
38	BACH1	chr1:46269216-46269229	H1-hESC	embryonic stem cell:	n/a	n/a
39	BACH1	chr1:46216255-46216359	K562	blood:	n/a	n/a
40	BACH1	chr1:46215889-46216589	H1-hESC	embryonic stem cell:	n/a	n/a
41	BACH1	chr1:46214815-46214916	K562	blood:	n/a	n/a
42	BATF	chr1:46216180-46216710	GM12878	blood:	n/a	n/a
43	BATF	chr1:46238528-46238854	GM12878	blood:	n/a	n/a
44	BATF	chr1:46306368-46306703	GM12878	blood:	n/a	n/a
45	BATF	chr1:46302487-46302754	GM12878	blood:	n/a	n/a
46	BATF	chr1:46308483-46308772	GM12878	blood:	n/a	n/a
47	BATF	chr1:46308522-46308841	GM12878	blood:	n/a	n/a
48	BATF	chr1:46268407-46268721	GM12878	blood:	n/a	chr1:46268569-46268579 chr1:46268635-46268648 chr1:46268568-46268579
49	BCLAF1	chr1:46302137-46302794	GM12878	blood:	n/a	n/a
50	BCLAF1	chr1:46215500-46216808	GM12878	blood:	n/a	chr1:46216050-46216059 chr1:46216121-46216134

(count:1469 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:46212773-46212823	ProgFib	skin:	n/a
2	chr1:46216399-46216449	AG04449	skin:	fetal
3	chr1:46265164-46265214	HRPEpiC	eye:	n/a
4	chr1:46265164-46265214	Hepatocyte	liver:	n/a
5	chr1:46216671-46216721	HRPEpiC	eye:	n/a
6	chr1:46212773-46212823	ProgFib	skin:	n/a
7	chr1:46216399-46216449	AG04449	skin:	fetal
8	chr1:46265164-46265214	HRPEpiC	eye:	n/a
9	chr1:46265164-46265214	Hepatocyte	liver:	n/a
10	chr1:46216671-46216721	HRPEpiC	eye:	n/a
11	chr1:46273758-46273808	CMK	blood:	n/a
12	chr1:46216609-46216659	NT2-D1	testis:	n/a
13	chr1:46216609-46216659	Jurkat	blood:	n/a
14	chr1:46215879-46215929	U87	brain:	n/a
15	chr1:46216671-46216721	A549	lung:	n/a
16	chr1:46220388-46220438	SKMC	muscle:	n/a
17	chr1:46212773-46212823	HCT-116	colon:	n/a
18	chr1:46269120-46269170	IMR90	lung:	fetal
19	chr1:46269394-46269444	LNCaP	prostate:	n/a
20	chr1:46216513-46216563	HCF	heart:	n/a
21	chr1:46216422-46216472	NH-A	brain:	n/a
22	chr1:46216737-46216787	Hela-S3	cervix:	n/a
23	chr1:46212773-46212823	Hepatocyte	liver:	n/a
24	chr1:46212773-46212823	GM19239	blood:	n/a
25	chr1:46269305-46269355	HUVEC	blood vessel:	n/a
26	chr1:46269324-46269374	AG04449	skin:	fetal
27	chr1:46212773-46212823	A549	lung:	n/a
28	chr1:46268158-46268208	ECC-1	luminal epithelium:	n/a
29	chr1:46216609-46216659	HRCEpiC	kidney:	n/a
30	chr1:46216195-46216245	ECC-1	luminal epithelium:	n/a
31	chr1:46216671-46216721	GM06990	blood:	n/a
32	chr1:46269397-46269447	HCT-116	colon:	n/a
33	chr1:46269120-46269170	HAEpiC	amniotic membrane:	n/a
34	chr1:46215776-46215826	HRPEpiC	eye:	n/a
35	chr1:46215957-46216007	HAEpiC	amniotic membrane:	n/a
36	chr1:46215776-46215826	MCF-7	breast:	n/a
37	chr1:46269788-46269838	ovcar-3	ovarian:	n/a
38	chr1:46273758-46273808	HRCEpiC	kidney:	n/a
39	chr1:46268207-46268257	NH-A	brain:	n/a
40	chr1:46267883-46267933	SK-N-SH_RA	brain:	n/a
41	chr1:46216671-46216721	NH-A	brain:	n/a
42	chr1:46212773-46212823	HRE	kidney:	n/a
43	chr1:46269788-46269838	BE2_C	brain:	n/a
44	chr1:46220388-46220438	IMR90	lung:	fetal
45	chr1:46216422-46216472	IMR90	lung:	fetal
46	chr1:46216399-46216449	Hela-S3	cervix:	n/a
47	chr1:46215957-46216007	ProgFib	skin:	n/a
48	chr1:46216422-46216472	HEK293	kidney:	embryo
49	chr1:46269394-46269444	GM19239	blood:	n/a
50	chr1:46216513-46216563	H1-hESC	embryonic stem cell:	embryo

(count:203 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr1:46215911..46216479-chr13:111521997..111522748,2	Hela-S3	cervix:
2	chr1:46215785..46216460-chr5:141302945..141303727,2	Hela-S3	cervix:
3	chr1:46241636..46244183-chr1:46246863..46248467,2	K562	blood:
4	chr1:46306882..46308441-chr1:46320292..46322525,2	K562	blood:
5	chr1:46215984..46216935-chr11:33757514..33758077,2	Hela-S3	cervix:
6	chr1:46268308..46270413-chr7:26238840..26240934,2	MCF-7	breast:
7	chr1:46319521..46322147-chr1:46326088..46328715,3	K562	blood:
8	chr1:46149977..46154848-chr1:46211592..46220262,26	K562	blood:
9	chr1:46280205..46283034-chr1:46287288..46288792,2	K562	blood:
10	chr1:46152480..46154825-chr1:46237407..46240193,2	K562	blood:
11	chr1:46205176..46207911-chr1:46209798..46211583,2	K562	blood:
12	chr1:46267846..46271685-chr1:46273024..46275916,3	MCF-7	breast:
13	chr1:46156649..46159424-chr1:46274017..46275928,2	K562	blood:
14	chr1:45196620..45197381-chr1:46216004..46216681,2	Hela-S3	cervix:
15	chr1:46330055..46331827-chr1:46334729..46336546,2	K562	blood:
16	chr1:45985982..45988652-chr1:46328949..46330795,2	K562	blood:
17	chr1:46329307..46330807-chr1:46606097..46608904,2	K562	blood:
18	chr1:46216513..46217350-chr19:17356305..17357058,2	Hela-S3	cervix:
19	chr1:45986653..45989205-chr1:46213742..46216155,2	K562	blood:
20	chr1:46341326..46343341-chr1:46347257..46349612,2	K562	blood:
21	chr1:46208187..46211922-chr1:46213576..46216674,3	MCF-7	breast:
22	chr1:46048521..46050568-chr1:46327605..46330996,3	K562	blood:
23	chr1:46215935..46216640-chr16:31191409..31192140,2	Hela-S3	cervix:
24	chr1:46319707..46321501-chr1:46343782..46345819,2	K562	blood:
25	chr1:46209131..46214084-chr1:46214242..46216334,5	K562	blood:
26	chr1:46267306..46271592-chr1:46272743..46276527,5	MCF-7	breast:
27	chr1:46258378..46261508-chr1:46262395..46264420,3	K562	blood:
28	chr1:46270044..46272656-chr1:46278992..46281641,2	K562	blood:
29	chr1:46216570..46222815-chr1:46224414..46229889,7	K562	blood:
30	chr1:46211582..46213293-chr1:46216678..46219405,2	MCF-7	breast:
31	chr1:46205421..46208484-chr1:46212688..46215517,5	K562	blood:
32	chr1:46151080..46154672-chr1:46265067..46271759,20	K562	blood:
33	chr1:46216117..46217904-chr1:46267595..46269245,2	MCF-7	breast:
34	chr1:46152211..46153942-chr1:46345305..46348053,3	K562	blood:
35	chr1:46268721..46270472-chr1:46322326..46324669,2	K562	blood:
36	chr1:46211470..46213214-chr1:46217609..46219595,2	K562	blood:
37	chr1:46151182..46154055-chr1:46326132..46330387,5	K562	blood:
38	chr1:46048559..46050395-chr1:46327197..46329514,2	MCF-7	breast:
39	chr1:46244095..46246858-chr1:46259918..46262871,2	K562	blood:
40	chr1:46219624..46221778-chr1:46224955..46227777,2	MCF-7	breast:
41	chr1:46151328..46153921-chr1:46205484..46208210,2	K562	blood:
42	chr1:46214695..46217648-chr1:46220779..46222795,3	K562	blood:
43	chr1:46273443..46277069-chr1:46280545..46283464,3	K562	blood:
44	chr1:46221868..46223615-chr1:46227697..46230065,2	K562	blood:
45	chr1:46214549..46216199-chr1:46228241..46229949,2	K562	blood:
46	chr1:46162572..46164263-chr1:46216730..46218266,2	K562	blood:
47	chr1:46268529..46274333-chr1:46275005..46281721,11	K562	blood:
48	chr1:46217664..46220133-chr1:46344829..46347460,2	K562	blood:
49	chr1:46195320..46197615-chr1:46201920..46204124,2	K562	blood:
50	chr1:46205176..46207911-chr1:46209798..46211583,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MAST2-3	chr1:46216682-46216920	NONHSAT002970
2	lnc-MAST2-3	chr1:46220237-46220295	NONHSAT002970

No data

Variant related genes	Relation type
MAST2	TF binding region
ENSG00000236111	TF binding region
IPP	TF binding region
TMA16P2	TF binding region
MAST2	CpG island
ENSG00000236111	CpG island
IPP	CpG island
TMA16P2	CpG island
ENSG00000081791	chromatin interactions
ENSG00000085063	chromatin interactions
ENSG00000117450	chromatin interactions
ENSG00000127463	chromatin interactions
ENSG00000121067	chromatin interactions
ENSG00000214756	chromatin interactions
ENSG00000202077	chromatin interactions
ENSG00000206597	chromatin interactions
ENSG00000260806	chromatin interactions
ENSG00000230896	chromatin interactions
ENSG00000114331	chromatin interactions
ENSG00000110321	chromatin interactions
ENSG00000053372	chromatin interactions
ENSG00000159592	chromatin interactions
ENSG00000159596	chromatin interactions
ENSG00000090060	chromatin interactions
ENSG00000255874	chromatin interactions
ENSG00000085999	chromatin interactions
ENSG00000236111	chromatin interactions
ENSG00000089280	chromatin interactions
ENSG00000139190	chromatin interactions
ENSG00000086015	chromatin interactions
ENSG00000160113	chromatin interactions
ENSG00000232467	chromatin interactions
ENSG00000132780	chromatin interactions
ENSG00000177606	chromatin interactions
ENSG00000085433	chromatin interactions
ENSG00000081870	chromatin interactions
ENSG00000163516	chromatin interactions
ENSG00000200169	chromatin interactions
ENSG00000247624	chromatin interactions
ENSG00000122565	chromatin interactions
ENSG00000137449	chromatin interactions
ENSG00000271122	chromatin interactions
ENSG00000122566	chromatin interactions
ENSG00000197429	chromatin interactions
ENSG00000122557	chromatin interactions

Extended variants
information (count: 5538 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:5538 , 50 per page) page: 1 2 3 4 5 6 7 ... 111

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs28433203	chr1:46196813-46196814	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs570357228	chr1:46196832-46196833	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs144471671	chr1:46196853-46196854	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs556048227	chr1:46196893-46196894	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs28525420	chr1:46196970-46196971	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs185428620	chr1:46196974-46196975	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs574694284	chr1:46197015-46197016	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs535862770	chr1:46197024-46197025	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs553913312	chr1:46197148-46197149	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs190285642	chr1:46197152-46197153	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs546366340	chr1:46197182-46197183	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs115292446	chr1:46197188-46197189	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs148431966	chr1:46197195-46197196	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs76298531	chr1:46197214-46197215	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs112389335	chr1:46197297-46197298	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs35824159	chr1:46197357-46197358	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs28675671	chr1:46197382-46197383	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs542746044	chr1:46197459-46197460	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs139934111	chr1:46197462-46197463	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs183330445	chr1:46197501-46197502	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs527374802	chr1:46197538-46197539	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs551890402	chr1:46197564-46197565	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs570271729	chr1:46197565-46197566	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs188786871	chr1:46197609-46197610	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs79709409	chr1:46197626-46197627	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs78860708	chr1:46197627-46197628	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs77750728	chr1:46197628-46197629	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs543770128	chr1:46197681-46197682	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs568359473	chr1:46197682-46197683	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs143466121	chr1:46197690-46197691	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs554135396	chr1:46197707-46197708	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs565981028	chr1:46197725-46197726	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs539901655	chr1:46197726-46197727	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs538447260	chr1:46197729-46197730	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs576684624	chr1:46197743-46197744	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs544048228	chr1:46197760-46197761	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs193027057	chr1:46197821-46197822	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs557497487	chr1:46197828-46197829	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs574251474	chr1:46197829-46197830	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs557798536	chr1:46197878-46197879	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs184153531	chr1:46197890-46197891	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs571422803	chr1:46197900-46197901	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs28490344	chr1:46197948-46197949	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs545446244	chr1:46197958-46197959	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs575100720	chr1:46197964-46197965	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs563858480	chr1:46197994-46197995	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs28513660	chr1:46197996-46197997	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs28498557	chr1:46198010-46198011	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs376905835	chr1:46198034-46198035	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs370840018	chr1:46198108-46198109	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:97)

Disease	PMID	Source
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21080181	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	17603634	CNVD
Soft tissue tumor	16732325	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic myeloid leukemia	21384125	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Uveal melanoma	20484589	CNVD
Ovarian cancer	22174824	CNVD
Muscle-eye-brain disease	21572526	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	20680643	CNVD
Colorectal cancer	19287155	CNVD
small cell lung cancer	20016488	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD
Ovarian cancer	17875760	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD

Chromatin state (count:2943 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:46154600-46206600	Weak transcription	Brain Substantia Nigra	brain
2	chr1:46155000-46215800	Weak transcription	Small Intestine	intestine
3	chr1:46155600-46204600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
4	chr1:46155800-46215600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
5	chr1:46156800-46203800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
6	chr1:46157400-46209800	Weak transcription	Brain Cingulate Gyrus	brain
7	chr1:46160800-46215400	Weak transcription	Brain Hippocampus Middle	brain
8	chr1:46161200-46206600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
9	chr1:46163600-46197400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr1:46163600-46215600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
11	chr1:46165600-46207000	Weak transcription	Colon Smooth Muscle	Colon
12	chr1:46174600-46206400	Weak transcription	Brain Germinal Matrix	brain
13	chr1:46174600-46215600	Weak transcription	Brain Angular Gyrus	brain
14	chr1:46174600-46215600	Weak transcription	Esophagus	oesophagus
15	chr1:46177800-46215600	Weak transcription	Gastric	stomach
16	chr1:46178000-46209200	Weak transcription	Skeletal Muscle Male	skeletal muscle
17	chr1:46178000-46209800	Weak transcription	Fetal Brain Male	brain
18	chr1:46178000-46209800	Weak transcription	Lung	lung
19	chr1:46178000-46215600	Weak transcription	Aorta	Aorta
20	chr1:46179600-46206400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr1:46179600-46209000	Weak transcription	Cortex derived primary cultured neurospheres	brain
22	chr1:46180400-46215600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
23	chr1:46181800-46215600	Weak transcription	Fetal Brain Female	brain
24	chr1:46182000-46203200	Weak transcription	Skeletal Muscle Female	skeletal muscle
25	chr1:46182000-46206600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
26	chr1:46182200-46215600	Weak transcription	Left Ventricle	heart
27	chr1:46182400-46206600	Weak transcription	Primary B cells from cord blood	blood
28	chr1:46182400-46206600	Weak transcription	Adipose Nuclei	Adipose
29	chr1:46184400-46201200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr1:46184400-46203200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
31	chr1:46185000-46206600	Weak transcription	Primary T helper cells PMA-I stimulated	--
32	chr1:46187200-46206800	Weak transcription	Fetal Lung	lung
33	chr1:46187400-46203800	Weak transcription	Primary T cells from cord blood	blood
34	chr1:46187400-46206600	Weak transcription	HSMM	muscle
35	chr1:46189200-46214800	Weak transcription	NHDF-Ad	bronchial
36	chr1:46189400-46207600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr1:46189400-46215400	Weak transcription	Muscle Satellite Cultured Cells	--
38	chr1:46192600-46206600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr1:46193000-46203200	Weak transcription	Spleen	Spleen
40	chr1:46193000-46209200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr1:46193400-46206200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
42	chr1:46193400-46207600	Weak transcription	Fetal Muscle Trunk	muscle
43	chr1:46193400-46208000	Weak transcription	Thymus	Thymus
44	chr1:46193600-46206400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr1:46193600-46206400	Weak transcription	Liver	Liver
46	chr1:46193600-46206400	Weak transcription	Rectal Mucosa Donor 29	rectum
47	chr1:46193600-46207800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr1:46193600-46215400	Weak transcription	Rectal Smooth Muscle	rectum
49	chr1:46193600-46215400	Weak transcription	HSMMtube	muscle
50	chr1:46193800-46197600	Weak transcription	Placenta Amnion	Placenta Amnion

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