Variant report

Variant	nsv541612
Chromosome Location	chr12:118599539-118732144
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1379)
CpG islands
(count:244)
Chromatin interactive
region (count:101)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1379 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:118620091-118620450	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:118725664-118726444	K562	blood:	n/a	n/a
3	ARID3A	chr12:118620107-118620331	K562	blood:	n/a	n/a
4	ARID3A	chr12:118659728-118660141	HepG2	liver:	n/a	n/a
5	ARID3A	chr12:118603025-118603194	HepG2	liver:	n/a	n/a
6	ARID3A	chr12:118619341-118619709	HepG2	liver:	n/a	n/a
7	ATF1	chr12:118620098-118620382	K562	blood:	n/a	n/a
8	ATF1	chr12:118726099-118726318	K562	blood:	n/a	n/a
9	ATF2	chr12:118604677-118605125	GM12878	blood:	n/a	n/a
10	ATF2	chr12:118604521-118605265	GM12878	blood:	n/a	n/a
11	BACH1	chr12:118626894-118626936	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr12:118612244-118612279	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr12:118715665-118716093	K562	blood:	n/a	n/a
14	BATF	chr12:118604602-118605156	GM12878	blood:	n/a	n/a
15	BATF	chr12:118643133-118643382	GM12878	blood:	n/a	n/a
16	BATF	chr12:118620105-118620367	GM12878	blood:	n/a	n/a
17	BATF	chr12:118635833-118636149	GM12878	blood:	n/a	n/a
18	BATF	chr12:118604653-118605092	GM12878	blood:	n/a	n/a
19	BATF	chr12:118689417-118689668	GM12878	blood:	n/a	n/a
20	BATF	chr12:118643632-118643914	GM12878	blood:	n/a	n/a
21	BCL11A	chr12:118674866-118675185	GM12878	blood:	n/a	chr12:118675058-118675067
22	BCL11A	chr12:118604669-118605098	GM12878	blood:	n/a	n/a
23	BCL11A	chr12:118643074-118643455	GM12878	blood:	n/a	n/a
24	BCL11A	chr12:118613927-118614235	GM12878	blood:	n/a	n/a
25	BCL11A	chr12:118604695-118605097	GM12878	blood:	n/a	n/a
26	BCL11A	chr12:118674790-118675224	GM12878	blood:	n/a	chr12:118675058-118675067
27	BCL11A	chr12:118643173-118643395	GM12878	blood:	n/a	n/a
28	BCL3	chr12:118658664-118658891	GM12878	blood:	n/a	n/a
29	BCL3	chr12:118604736-118605113	GM12878	blood:	n/a	n/a
30	BCLAF1	chr12:118643562-118644068	GM12878	blood:	n/a	n/a
31	BCLAF1	chr12:118604594-118605163	GM12878	blood:	n/a	n/a
32	BCLAF1	chr12:118674680-118675262	GM12878	blood:	n/a	chr12:118675058-118675067
33	BCLAF1	chr12:118604532-118605164	GM12878	blood:	n/a	n/a
34	BCLAF1	chr12:118620009-118620417	GM12878	blood:	n/a	n/a
35	BHLHE40	chr12:118604653-118605543	GM12878	blood:	n/a	n/a
36	BHLHE40	chr12:118621095-118621260	GM12878	blood:	n/a	n/a
37	BHLHE40	chr12:118619503-118619643	GM12878	blood:	n/a	n/a
38	BHLHE40	chr12:118620100-118620295	K562	blood:	n/a	n/a
39	BHLHE40	chr12:118614026-118614192	GM12878	blood:	n/a	n/a
40	BRCA1	chr12:118620094-118620304	Hela-S3	cervix:	n/a	n/a
41	CBX3	chr12:118709511-118710067	HCT-116	colon:	n/a	n/a
42	CEBPB	chr12:118709615-118709943	ECC-1	luminal epithelium:	n/a	n/a
43	CEBPB	chr12:118650039-118650304	A549	lung:	n/a	n/a
44	CEBPB	chr12:118620107-118620486	Hela-S3	cervix:	n/a	chr12:118620314-118620325
45	CEBPB	chr12:118709525-118710026	HCT-116	colon:	n/a	n/a
46	CEBPB	chr12:118709645-118710013	ECC-1	luminal epithelium:	n/a	n/a
47	CEBPB	chr12:118688687-118688792	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr12:118620125-118620471	K562	blood:	n/a	chr12:118620314-118620325
49	CEBPB	chr12:118607519-118607665	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr12:118620063-118620501	MCF-7	breast:	n/a	chr12:118620314-118620325

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:118620216-118620266	AG09319	gingival:	n/a
2	chr12:118728016-118728066	NHDF-neo	bronchial:	n/a
3	chr12:118627943-118627993	SK-N-SH	brain:	n/a
4	chr12:118620216-118620266	SK-N-SH_RA	brain:	n/a
5	chr12:118620216-118620266	HRPEpiC	eye:	n/a
6	chr12:118627943-118627993	GM06990	blood:	n/a
7	chr12:118728016-118728066	HUVEC	blood vessel:	n/a
8	chr12:118728016-118728066	PFSK-1	brain:	n/a
9	chr12:118620216-118620266	HCM	heart:	n/a
10	chr12:118683952-118684002	ProgFib	skin:	n/a
11	chr12:118683952-118684002	SK-N-SH_RA	brain:	n/a
12	chr12:118627943-118627993	MCF-7	breast:	n/a
13	chr12:118627943-118627993	NHBE	bronchial:	n/a
14	chr12:118728016-118728066	PrEC	prostate:	n/a
15	chr12:118683952-118684002	NHDF-neo	bronchial:	n/a
16	chr12:118728016-118728066	HepG2	liver:	n/a
17	chr12:118620216-118620266	HEK293	kidney:	embryo
18	chr12:118728016-118728066	HCT-116	colon:	n/a
19	chr12:118728016-118728066	GM12878	blood:	n/a
20	chr12:118683952-118684002	HMEC	breast:	n/a
21	chr12:118728016-118728066	GM12891	blood:	n/a
22	chr12:118683952-118684002	IMR90	lung:	fetal
23	chr12:118620216-118620266	SK-N-SH	brain:	n/a
24	chr12:118620216-118620266	GM19239	blood:	n/a
25	chr12:118728016-118728066	AoSMC	blood vessel:	n/a
26	chr12:118627943-118627993	NH-A	brain:	n/a
27	chr12:118620216-118620266	AG04450	lung:	fetal
28	chr12:118627943-118627993	ECC-1	luminal epithelium:	n/a
29	chr12:118728016-118728066	SKMC	muscle:	n/a
30	chr12:118620216-118620266	ovcar-3	ovarian:	n/a
31	chr12:118683952-118684002	NH-A	brain:	n/a
32	chr12:118627943-118627993	GM12891	blood:	n/a
33	chr12:118627943-118627993	ovcar-3	ovarian:	n/a
34	chr12:118728016-118728066	HRE	kidney:	n/a
35	chr12:118627943-118627993	H1-hESC	embryonic stem cell:	embryo
36	chr12:118627943-118627993	AG10803	skin:	n/a
37	chr12:118683952-118684002	GM06990	blood:	n/a
38	chr12:118683952-118684002	ovcar-3	ovarian:	n/a
39	chr12:118683952-118684002	NT2-D1	testis:	n/a
40	chr12:118728016-118728066	AG09309	skin:	n/a
41	chr12:118620216-118620266	HIPEpiC	eye:	n/a
42	chr12:118683952-118684002	H1-hESC	embryonic stem cell:	embryo
43	chr12:118620216-118620266	MCF-7	breast:	n/a
44	chr12:118627943-118627993	NT2-D1	testis:	n/a
45	chr12:118728016-118728066	Hela-S3	cervix:	n/a
46	chr12:118620216-118620266	SK-N-MC	brain:	n/a
47	chr12:118627943-118627993	AG09309	skin:	n/a
48	chr12:118620216-118620266	RPTEC	kidney:	n/a
49	chr12:118728016-118728066	A549	lung:	n/a
50	chr12:118620216-118620266	GM12891	blood:	n/a

(count:101 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr12:118718803..118721131-chr12:118813506..118815349,2	K562	blood:
2	chr12:118602901..118604685-chr12:118608153..118610570,2	K562	blood:
3	chr12:118607954..118611154-chr12:118618350..118620487,3	MCF-7	breast:
4	chr12:118607954..118611154-chr12:118618350..118620487,3	MCF-7	breast:
5	chr12:118618995..118624149-chr12:118809534..118814465,7	K562	blood:
6	chr12:118674498..118676641-chr12:118709744..118711259,2	MCF-7	breast:
7	chr12:118629113..118632294-chr12:118813183..118816141,3	MCF-7	breast:
8	chr12:118596811..118599066-chr12:118602668..118604454,2	MCF-7	breast:
9	chr12:118676214..118678466-chr12:118707560..118709083,2	MCF-7	breast:
10	chr12:118718687..118720967-chr12:118721247..118724156,2	MCF-7	breast:
11	chr12:118558430..118559056-chr12:118602563..118603381,3	MCF-7	breast:
12	chr12:118666340..118669274-chr12:118811225..118812911,2	MCF-7	breast:
13	chr12:118498765..118502129-chr12:118621622..118623840,3	K562	blood:
14	chr12:118573812..118576177-chr12:118596570..118599987,3	K562	blood:
15	chr12:118618547..118621544-chr12:118809658..118815729,8	MCF-7	breast:
16	chr12:118602638..118603497-chr12:118815737..118816345,4	MCF-7	breast:
17	chr12:118674302..118676883-chr12:118810896..118813058,3	MCF-7	breast:
18	chr12:118572856..118575962-chr12:118597469..118600285,3	K562	blood:
19	chr12:118638724..118640594-chr12:118810784..118812979,2	K562	blood:
20	chr12:118609610..118611616-chr12:118813657..118815743,2	MCF-7	breast:
21	chr12:118616609..118618559-chr12:118621695..118624437,2	K562	blood:
22	chr12:118621945..118622509-chr12:118813550..118814054,2	K562	blood:
23	chr12:118727163..118729495-chr12:118743311..118746203,2	K562	blood:
24	chr12:118621252..118623142-chr12:118808957..118811612,2	K562	blood:
25	chr12:118636493..118639224-chr12:118810079..118811785,2	MCF-7	breast:
26	chr12:118690956..118692482-chr12:118706042..118708057,2	K562	blood:
27	chr12:118619511..118620730-chr12:118813675..118814689,5	K562	blood:
28	chr12:118626372..118631667-chr12:118631943..118636287,5	K562	blood:
29	chr12:118670359..118672856-chr12:118680813..118682507,2	K562	blood:
30	chr12:118728193..118730845-chr12:118739160..118741836,2	K562	blood:
31	chr12:118620159..118620747-chr12:118814583..118815397,2	MCF-7	breast:
32	chr12:118619592..118620348-chr3:46120462..46121012,2	MCF-7	breast:
33	chr12:118676214..118678466-chr12:118707560..118709083,2	MCF-7	breast:
34	chr12:118673643..118676401-chr12:118686637..118689650,3	K562	blood:
35	chr12:118618991..118620730-chr12:118813556..118814542,16	MCF-7	breast:
36	chr12:118607204..118610139-chr12:118612001..118614626,2	K562	blood:
37	chr12:118691774..118694683-chr12:118713486..118715660,2	K562	blood:
38	chr12:118613530..118616835-chr12:118807216..118810760,3	MCF-7	breast:
39	chr12:118629722..118631578-chr12:118673558..118677291,3	K562	blood:
40	chr12:118620907..118623414-chr12:118626921..118629279,2	K562	blood:
41	chr12:118629722..118631578-chr12:118673558..118677291,3	K562	blood:
42	chr12:118687145..118690867-chr12:118809484..118812867,4	K562	blood:
43	chr12:118712134..118713954-chr12:118730833..118733395,2	MCF-7	breast:
44	chr12:118598981..118601040-chr12:118601052..118602863,2	MCF-7	breast:
45	chr12:118709106..118711234-chr12:118810302..118813742,3	MCF-7	breast:
46	chr12:118624725..118628075-chr12:118814088..118815876,3	K562	blood:
47	chr12:118637134..118639756-chr12:118657925..118660314,3	MCF-7	breast:
48	chr12:118685088..118687913-chr12:118695342..118697547,2	MCF-7	breast:
49	chr12:118673323..118676031-chr12:118677378..118679199,2	MCF-7	breast:
50	chr12:118688074..118690965-chr12:118809730..118812650,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-VSIG10-1	chr12:118612199-118612678	ENSG00000249477
2	lnc-VSIG10-1	chr12:118613267-118614556	ENSG00000249477
3	lnc-VSIG10-2	chr12:118633213-118633590	expReg_chr12_10373_-
4	lnc-VSIG10-4	chr12:118699302-118699478	NONHSAT031036
5	lnc-VSIG10-4	chr12:118704460-118704564	NONHSAT031036
6	lnc-VSIG10-4	chr12:118693401-118693460	NONHSAT031036

No data

Variant related genes	Relation type
RPS2P5	TF binding region
TAOK3	TF binding region
ENSG00000221280	TF binding region
RPS2P5	CpG island
TAOK3	CpG island
ENSG00000221280	CpG island
ENSG00000089220	chromatin interactions
ENSG00000176871	chromatin interactions
ENSG00000176834	chromatin interactions
ENSG00000221280	chromatin interactions
ENSG00000135090	chromatin interactions
ENSG00000270482	chromatin interactions
ENSG00000111707	chromatin interactions

Extended variants
information (count: 4417 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:4417 , 50 per page) page: 1 2 3 4 5 6 7 ... 89

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs201354242	chr12:118599551-118599552	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs374287867	chr12:118599558-118599559	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs375879690	chr12:118599655-118599656	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs535535786	chr12:118599656-118599657	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs141234841	chr12:118599695-118599696	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs267603331	chr12:118599706-118599707	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs369814549	chr12:118599718-118599719	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs373274877	chr12:118599735-118599736	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs150771877	chr12:118599758-118599759	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs375121760	chr12:118599764-118599765	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs369335110	chr12:118599776-118599777	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs75606682	chr12:118599837-118599838	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs377135848	chr12:118599857-118599858	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs370220337	chr12:118599858-118599859	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs201446583	chr12:118599865-118599866	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs531106799	chr12:118599924-118599925	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs149398919	chr12:118599935-118599936	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs144799784	chr12:118600002-118600003	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs544531908	chr12:118600009-118600010	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs564193553	chr12:118600072-118600073	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs563606893	chr12:118600087-118600088	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs544840080	chr12:118600092-118600093	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs138184791	chr12:118600098-118600099	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs36124656	chr12:118600136-118600137	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs561430192	chr12:118600137-118600138	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs148533205	chr12:118600153-118600154	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs559428833	chr12:118600198-118600199	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs528602159	chr12:118600201-118600202	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs17586342	chr12:118600204-118600205	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs561969719	chr12:118600231-118600232	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs546898240	chr12:118600239-118600240	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs530995958	chr12:118600273-118600274	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs551272139	chr12:118600306-118600307	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs529420077	chr12:118600309-118600310	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs189228488	chr12:118600310-118600311	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs546660547	chr12:118600327-118600328	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs566956654	chr12:118600347-118600348	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs532696810	chr12:118600354-118600355	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs535572541	chr12:118600406-118600407	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs113477587	chr12:118600409-118600410	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs17619569	chr12:118600414-118600415	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs146047885	chr12:118600420-118600421	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs547524528	chr12:118600450-118600451	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs191764526	chr12:118600466-118600467	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs61943527	chr12:118600468-118600469	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs140025506	chr12:118600488-118600489	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs184271489	chr12:118600608-118600609	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs189098863	chr12:118600647-118600648	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs572877440	chr12:118600678-118600679	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs75676957	chr12:118600737-118600738	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:74)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Cancer	16751803	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
Wilms tumour	21544195	CNVD
Ovarian cancer	21720365	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	17603634	CNVD
Breast cancer	16397240	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	17133270	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Cryptorchidism	21048976	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Neuroblastoma	20406844	CNVD
Medulloblastoma	16783165	CNVD
mental retardation	16760730	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21364760	CNVD
Lung adenocarcinoma	21045234	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21806811	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	18511947	CNVD

Chromatin state (count:2769 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:118575600-118601600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr12:118576000-118601200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr12:118576000-118619600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
4	chr12:118576000-118624000	Weak transcription	Stomach Mucosa	stomach
5	chr12:118577400-118601800	Strong transcription	Cortex derived primary cultured neurospheres	brain
6	chr12:118578200-118611600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr12:118578600-118603200	Weak transcription	Pancreatic Islets	Pancreatic Islet
8	chr12:118584000-118627600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr12:118585600-118603000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr12:118585800-118619000	Weak transcription	HepG2	liver
11	chr12:118586200-118601000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr12:118586200-118619400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr12:118586600-118613600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr12:118586800-118600400	Strong transcription	Primary neutrophils fromperipheralblood	blood
15	chr12:118586800-118600800	Strong transcription	Primary monocytes fromperipheralblood	blood
16	chr12:118586800-118601400	Strong transcription	Monocytes-CD14+_RO01746	blood
17	chr12:118586800-118603600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
18	chr12:118587000-118600400	Strong transcription	Primary T cells from cord blood	blood
19	chr12:118587600-118611200	Weak transcription	HUES6 Cell Line	embryonic stem cell
20	chr12:118587600-118619200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr12:118587800-118620000	Weak transcription	HUES64 Cell Line	embryonic stem cell
22	chr12:118589000-118601200	Strong transcription	Primary B cells from peripheral blood	blood
23	chr12:118589400-118601200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr12:118589600-118619000	Weak transcription	A549	lung
25	chr12:118590400-118617000	Weak transcription	H9 Cell Line	embryonic stem cell
26	chr12:118592600-118619400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr12:118593000-118601200	Strong transcription	Primary hematopoietic stem cells	blood
28	chr12:118593200-118600400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr12:118593200-118619200	Strong transcription	Fetal Brain Female	brain
30	chr12:118593200-118619400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
31	chr12:118593200-118619600	Strong transcription	Primary T cells fromperipheralblood	blood
32	chr12:118593400-118600400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr12:118593600-118600000	Strong transcription	Fetal Stomach	stomach
34	chr12:118593600-118600400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
35	chr12:118593600-118600600	Strong transcription	Primary T helper cells fromperipheralblood	blood
36	chr12:118593600-118601600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr12:118593800-118600200	Strong transcription	Rectal Mucosa Donor 31	rectum
38	chr12:118593800-118600400	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
39	chr12:118593800-118600400	Strong transcription	Liver	Liver
40	chr12:118593800-118600400	Strong transcription	Left Ventricle	heart
41	chr12:118594000-118600000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr12:118594000-118600400	Strong transcription	NHEK	skin
43	chr12:118594000-118601200	Strong transcription	Brain Germinal Matrix	brain
44	chr12:118594000-118601200	Strong transcription	Rectal Mucosa Donor 29	rectum
45	chr12:118594400-118600200	Strong transcription	Thymus	Thymus
46	chr12:118594600-118600000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr12:118594800-118600200	Strong transcription	Primary B cells from cord blood	blood
48	chr12:118594800-118600200	Strong transcription	Duodenum Smooth Muscle	Duodenum
49	chr12:118595000-118599800	Strong transcription	HSMMtube	muscle
50	chr12:118595000-118600000	Strong transcription	Fetal Muscle Leg	muscle

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