Variant report

Variant	nsv516587
Chromosome Location	chr9:86226119-86255765
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1115)
CpG islands
(count:428)
Chromatin interactive
region (count:56)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1115 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:86226466-86226789	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:86238855-86239052	K562	blood:	n/a	n/a
3	ARID3A	chr9:86244472-86245078	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:86235683-86236452	HepG2	liver:	n/a	n/a
5	ARID3A	chr9:86226439-86226702	K562	blood:	n/a	n/a
6	ATF2	chr9:86246112-86246455	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr9:86226431-86226686	K562	blood:	n/a	n/a
8	BCLAF1	chr9:86237789-86238553	GM12878	blood:	n/a	chr9:86237988-86238001 chr9:86238011-86238020 chr9:86238184-86238193 chr9:86238181-86238190
9	BCLAF1	chr9:86237581-86238703	GM12878	blood:	n/a	chr9:86237988-86238001 chr9:86238011-86238020 chr9:86238184-86238193 chr9:86238181-86238190
10	BHLHE40	chr9:86235749-86236425	HepG2	liver:	n/a	n/a
11	BHLHE40	chr9:86244498-86245027	HepG2	liver:	n/a	n/a
12	BHLHE40	chr9:86238529-86238730	K562	blood:	n/a	n/a
13	BHLHE40	chr9:86237852-86238126	K562	blood:	n/a	chr9:86237988-86238004
14	CCNT2	chr9:86246163-86246261	K562	blood:	n/a	n/a
15	CCNT2	chr9:86237895-86238638	K562	blood:	n/a	n/a
16	CEBPB	chr9:86231394-86231493	HepG2	liver:	n/a	chr9:86231406-86231417
17	CEBPB	chr9:86235754-86235954	HepG2	liver:	n/a	n/a
18	CEBPB	chr9:86231322-86231464	K562	blood:	n/a	chr9:86231406-86231417
19	CEBPB	chr9:86235625-86236007	K562	blood:	n/a	n/a
20	CEBPB	chr9:86238262-86238454	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr9:86237819-86237963	HepG2	liver:	n/a	n/a
22	CEBPB	chr9:86226418-86226705	H1-hESC	embryonic stem cell:	n/a	chr9:86226541-86226554 chr9:86226541-86226552 chr9:86226542-86226553 chr9:86226541-86226554
23	CEBPB	chr9:86238767-86239165	K562	blood:	n/a	n/a
24	CEBPB	chr9:86226341-86227098	Hela-S3	cervix:	n/a	chr9:86226541-86226554 chr9:86226541-86226552 chr9:86226542-86226553 chr9:86226541-86226554
25	CEBPB	chr9:86237789-86237994	A549	lung:	n/a	n/a
26	CEBPB	chr9:86244497-86245017	HepG2	liver:	n/a	n/a
27	CEBPB	chr9:86226399-86226681	K562	blood:	n/a	chr9:86226541-86226554 chr9:86226541-86226552 chr9:86226542-86226553 chr9:86226541-86226554
28	CEBPB	chr9:86235584-86236003	A549	lung:	n/a	n/a
29	CEBPB	chr9:86226323-86226883	MCF-7	breast:	n/a	chr9:86226541-86226554 chr9:86226541-86226552 chr9:86226542-86226553 chr9:86226541-86226554
30	CEBPB	chr9:86235669-86235989	IMR90	lung:	n/a	n/a
31	CEBPB	chr9:86243495-86243704	A549	lung:	n/a	chr9:86243619-86243632 chr9:86243620-86243631
32	CEBPB	chr9:86226225-86226842	MCF-7	breast:	n/a	chr9:86226541-86226554 chr9:86226541-86226552 chr9:86226542-86226553 chr9:86226541-86226554
33	CEBPB	chr9:86235665-86236019	HepG2	liver:	n/a	n/a
34	CEBPB	chr9:86231288-86231525	IMR90	lung:	n/a	chr9:86231406-86231417
35	CEBPB	chr9:86226394-86226727	HepG2	liver:	n/a	chr9:86226541-86226554 chr9:86226541-86226552 chr9:86226542-86226553 chr9:86226541-86226554
36	CEBPB	chr9:86243530-86243785	HepG2	liver:	n/a	chr9:86243619-86243632 chr9:86243620-86243631
37	CEBPB	chr9:86235691-86235975	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr9:86226395-86226690	A549	lung:	n/a	chr9:86226541-86226554 chr9:86226541-86226552 chr9:86226542-86226553 chr9:86226541-86226554
39	CEBPB	chr9:86237766-86238283	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr9:86226339-86226733	K562	blood:	n/a	chr9:86226541-86226554 chr9:86226541-86226552 chr9:86226542-86226553 chr9:86226541-86226554
41	CEBPB	chr9:86226399-86226605	K562	blood:	n/a	chr9:86226541-86226554 chr9:86226541-86226552 chr9:86226542-86226553 chr9:86226541-86226554
42	CEBPB	chr9:86235611-86236077	MCF-7	breast:	n/a	n/a
43	CEBPD	chr9:86237597-86238227	HepG2	liver:	n/a	n/a
44	CEBPD	chr9:86244767-86245132	HepG2	liver:	n/a	n/a
45	CEBPZ	chr9:86240782-86240814	HepG2	liver:	n/a	n/a
46	CHD1	chr9:86238062-86238251	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD1	chr9:86237495-86239059	GM12878	blood:	n/a	n/a
48	CHD2	chr9:86238024-86238216	HepG2	liver:	n/a	n/a
49	CHD2	chr9:86244428-86244432	HepG2	liver:	n/a	n/a
50	CHD2	chr9:86238464-86238909	HepG2	liver:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:86237590-86237640	HCF	heart:	n/a
2	chr9:86237590-86237640	HCF	heart:	n/a
3	chr9:86240166-86240216	PANC-1	pancreas:	n/a
4	chr9:86236624-86236674	Hepatocyte	liver:	n/a
5	chr9:86236624-86236674	HepG2	liver:	n/a
6	chr9:86238535-86238585	MCF10A-Er-Src	breast:	n/a
7	chr9:86236624-86236674	NHBE	bronchial:	n/a
8	chr9:86240166-86240216	SK-N-SH_RA	brain:	n/a
9	chr9:86244969-86245019	SKMC	muscle:	n/a
10	chr9:86237590-86237640	Hela-S3	cervix:	n/a
11	chr9:86238535-86238585	HAEpiC	amniotic membrane:	n/a
12	chr9:86238535-86238585	AG04449	skin:	fetal
13	chr9:86237590-86237640	Jurkat	blood:	n/a
14	chr9:86236624-86236674	CMK	blood:	n/a
15	chr9:86244969-86245019	K562	blood:	n/a
16	chr9:86236624-86236674	HCT-116	colon:	n/a
17	chr9:86236624-86236674	GM12878	blood:	n/a
18	chr9:86238119-86238169	HEK293	kidney:	embryo
19	chr9:86237793-86237843	GM19239	blood:	n/a
20	chr9:86238119-86238169	GM19239	blood:	n/a
21	chr9:86238535-86238585	HUVEC	blood vessel:	n/a
22	chr9:86238535-86238585	Caco-2	colon:	n/a
23	chr9:86237793-86237843	AG04450	lung:	fetal
24	chr9:86238535-86238585	NH-A	brain:	n/a
25	chr9:86236624-86236674	PANC-1	pancreas:	n/a
26	chr9:86238535-86238585	PANC-1	pancreas:	n/a
27	chr9:86244969-86245019	Hela-S3	cervix:	n/a
28	chr9:86238119-86238169	GM12892	blood:	n/a
29	chr9:86236624-86236674	GM12892	blood:	n/a
30	chr9:86240166-86240216	HPAEpiC	pulmonary alveolar:	n/a
31	chr9:86238119-86238169	Caco-2	colon:	n/a
32	chr9:86236624-86236674	AoSMC	blood vessel:	n/a
33	chr9:86237793-86237843	Hela-S3	cervix:	n/a
34	chr9:86238535-86238585	ovcar-3	ovarian:	n/a
35	chr9:86238119-86238169	HEEpiC	esophagus:	n/a
36	chr9:86236624-86236674	AG04449	skin:	fetal
37	chr9:86237590-86237640	ovcar-3	ovarian:	n/a
38	chr9:86238535-86238585	HNPCEpiC	eye:	n/a
39	chr9:86237793-86237843	U87	brain:	n/a
40	chr9:86238119-86238169	CMK	blood:	n/a
41	chr9:86237793-86237843	Caco-2	colon:	n/a
42	chr9:86238119-86238169	PANC-1	pancreas:	n/a
43	chr9:86244969-86245019	Jurkat	blood:	n/a
44	chr9:86237793-86237843	RPTEC	kidney:	n/a
45	chr9:86244969-86245019	Hepatocyte	liver:	n/a
46	chr9:86236624-86236674	GM06990	blood:	n/a
47	chr9:86237590-86237640	ECC-1	luminal epithelium:	n/a
48	chr9:86238535-86238585	AG04450	lung:	fetal
49	chr9:86237793-86237843	AG04449	skin:	fetal
50	chr9:86236624-86236674	ECC-1	luminal epithelium:	n/a

(count:56 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr9:86231903..86234223-chr9:86234502..86236689,2	MCF-7	breast:
2	chr9:86236918..86239524-chr9:86322198..86323756,2	K562	blood:
3	chr9:86248664..86251363-chr9:86251483..86253533,2	MCF-7	breast:
4	chr9:86251432..86253303-chr9:86255236..86258131,2	MCF-7	breast:
5	chr9:86215991..86217678-chr9:86226760..86228301,2	MCF-7	breast:
6	chr6:75994626..75995177-chr9:86238029..86238568,2	Hela-S3	cervix:
7	chr9:86236280..86241962-chr9:86320992..86325340,9	MCF-7	breast:
8	chr9:86248664..86251363-chr9:86251483..86253533,2	MCF-7	breast:
9	chr9:86230487..86233014-chr9:86237019..86239739,2	MCF-7	breast:
10	chr9:86236830..86238714-chr9:86253214..86255307,2	K562	blood:
11	chr9:86234634..86237562-chr9:86262513..86264120,2	MCF-7	breast:
12	chr9:86231309..86235233-chr9:86236386..86239078,4	MCF-7	breast:
13	chr16:73080234..73082394-chr9:86236447..86238062,2	MCF-7	breast:
14	chr9:86235893..86237501-chr9:86238448..86240518,2	MCF-7	breast:
15	chr9:86238599..86242233-chr9:86242446..86245459,4	K562	blood:
16	chr9:86229963..86232786-chr9:86243072..86244741,2	K562	blood:
17	chr9:86244110..86246714-chr9:86535414..86538304,2	K562	blood:
18	chr9:86235832..86238192-chr9:86245437..86248685,3	K562	blood:
19	chr9:86237033..86239481-chr9:86571525..86573399,2	MCF-7	breast:
20	chr9:86235210..86236113-chr9:86451876..86452442,2	MCF-7	breast:
21	chr9:86247178..86252278-chr9:86254565..86260519,7	MCF-7	breast:
22	chr9:86249075..86251124-chr9:86419195..86422058,2	K562	blood:
23	chr9:86249957..86252559-chr9:86321303..86324119,2	MCF-7	breast:
24	chr9:86236616..86242493-chr9:86533666..86537484,7	MCF-7	breast:
25	chr9:86255011..86257353-chr9:86257547..86260085,2	MCF-7	breast:
26	chr9:86243220..86245781-chr9:86323093..86324779,2	MCF-7	breast:
27	chr9:86251932..86254568-chr9:86256964..86260409,3	K562	blood:
28	chr9:86225757..86228159-chr9:86237924..86239519,2	K562	blood:
29	chr9:86230729..86232939-chr9:86244046..86245933,2	K562	blood:
30	chr9:86248086..86250305-chr9:86262008..86265514,3	MCF-7	breast:
31	chr9:86247034..86248660-chr9:86250680..86252326,2	K562	blood:
32	chr9:86243566..86245560-chr9:86258572..86260267,2	MCF-7	breast:
33	chr9:86210303..86212582-chr9:86243491..86245294,2	MCF-7	breast:
34	chr9:86245520..86247823-chr9:86535695..86537836,2	MCF-7	breast:
35	chr9:86251432..86253303-chr9:86255236..86258131,2	MCF-7	breast:
36	chr9:86231903..86234223-chr9:86234502..86236689,2	MCF-7	breast:
37	chr9:86237271..86239294-chr9:86534482..86537409,3	MCF-7	breast:
38	chr9:86252769..86254326-chr9:86257407..86258944,2	K562	blood:
39	chr6:151712214..151713783-chr9:86237532..86239422,2	MCF-7	breast:
40	chr9:86235404..86236308-chr9:86263503..86264783,10	MCF-7	breast:
41	chr9:86235893..86237501-chr9:86238448..86240518,2	MCF-7	breast:
42	chr9:86235380..86236670-chr9:86263664..86264678,5	K562	blood:
43	chr9:86224413..86228341-chr9:86234250..86239512,5	MCF-7	breast:
44	chr9:86238599..86242233-chr9:86242446..86245459,4	K562	blood:
45	chr9:86229963..86232786-chr9:86243072..86244741,2	K562	blood:
46	chr9:86235380..86236346-chr9:86263721..86264658,5	MCF-7	breast:
47	chr9:86241062..86243617-chr9:86248330..86250163,2	K562	blood:
48	chr9:86241062..86243617-chr9:86248330..86250163,2	K562	blood:
49	chr9:86244611..86247023-chr9:86320465..86322962,2	MCF-7	breast:
50	chr9:86247178..86252278-chr9:86254565..86260519,7	MCF-7	breast:

No data

Variant related genes	Relation type
IDNK	TF binding region
IDNK	CpG island
ENSG00000112697	chromatin interactions
ENSG00000165115	chromatin interactions
ENSG00000165118	chromatin interactions
ENSG00000254473	chromatin interactions
ENSG00000225793	chromatin interactions
ENSG00000199483	chromatin interactions
ENSG00000181472	chromatin interactions
ENSG00000135018	chromatin interactions
ENSG00000140836	chromatin interactions
ENSG00000226877	chromatin interactions
ENSG00000148057	chromatin interactions

Extended variants
information (count: 1028 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:1028 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7865279	chr9:86226119-86226120	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs186287705	chr9:86226120-86226121	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs533192949	chr9:86226131-86226132	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs558093279	chr9:86226251-86226252	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs533822996	chr9:86226326-86226327	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs75116520	chr9:86226327-86226328	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs570403651	chr9:86226386-86226387	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs571714584	chr9:86226406-86226407	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs375985907	chr9:86226492-86226493	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs537416703	chr9:86226512-86226513	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs190668376	chr9:86226522-86226523	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs182991284	chr9:86226560-86226561	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs536844302	chr9:86226565-86226566	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs555198028	chr9:86226566-86226567	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs573621287	chr9:86226713-86226714	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs113275498	chr9:86226724-86226725	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs565165327	chr9:86226743-86226744	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs577182587	chr9:86226744-86226745	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs199841513	chr9:86226768-86226769	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs544237996	chr9:86226849-86226850	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs543282603	chr9:86226871-86226872	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs563001576	chr9:86226916-86226917	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs530133785	chr9:86226932-86226933	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs371368948	chr9:86226979-86226980	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs147767268	chr9:86226980-86226981	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs200854752	chr9:86227016-86227017	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs187330937	chr9:86227017-86227018	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs201992892	chr9:86227018-86227019	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs563522791	chr9:86227041-86227042	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs531678149	chr9:86227081-86227082	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs373065566	chr9:86227129-86227130	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs376630707	chr9:86227159-86227160	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs149135232	chr9:86227210-86227211	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs546959687	chr9:86227235-86227236	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs552073986	chr9:86227269-86227270	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs570622945	chr9:86227270-86227271	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs144662929	chr9:86227380-86227381	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs192645012	chr9:86227403-86227404	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs568194336	chr9:86227466-86227467	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs535535736	chr9:86227575-86227576	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs555236882	chr9:86227593-86227594	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs573454490	chr9:86227613-86227614	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs534354304	chr9:86227674-86227675	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs182999988	chr9:86227748-86227749	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs10868034	chr9:86227783-86227784	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs187655189	chr9:86227800-86227801	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs11140175	chr9:86227850-86227851	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs10746716	chr9:86227877-86227878	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs148132578	chr9:86227922-86227923	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs560184512	chr9:86227923-86227924	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Leukemia	18688285	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Bipolar disorder	18458673	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
Urothelial cell carcinoma	18451213	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Renal cell carcinoma	18765545	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1068 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:86216200-86237400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr9:86224800-86226600	Weak transcription	HepG2	liver
3	chr9:86225600-86226200	Weak transcription	Fetal Intestine Small	intestine
4	chr9:86225800-86226400	Enhancers	Liver	Liver
5	chr9:86226200-86226600	Enhancers	Hela-S3	cervix
6	chr9:86226200-86226800	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr9:86226200-86226800	Enhancers	Primary hematopoietic stem cells short term culture	blood
8	chr9:86226200-86227000	Enhancers	Primary hematopoietic stem cells	blood
9	chr9:86226200-86227000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr9:86226400-86227000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr9:86226400-86227000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr9:86226400-86227000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr9:86226400-86227400	Flanking Active TSS	Liver	Liver
14	chr9:86226600-86226800	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr9:86226600-86226800	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr9:86226600-86226800	Enhancers	Fetal Intestine Large	intestine
17	chr9:86226600-86226800	Active TSS	Pancreatic Islets	Pancreatic Islet
18	chr9:86226600-86226800	Enhancers	Pancreas	Pancrea
19	chr9:86226600-86227000	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr9:86226600-86227000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr9:86226600-86227000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
22	chr9:86226600-86227000	Enhancers	Fetal Heart	heart
23	chr9:86226600-86227000	Flanking Active TSS	Hela-S3	cervix
24	chr9:86226600-86227000	Enhancers	HepG2	liver
25	chr9:86226800-86227000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr9:86226800-86227000	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
27	chr9:86226800-86227000	Bivalent Enhancer	Fetal Lung	lung
28	chr9:86227000-86227200	Enhancers	Hela-S3	cervix
29	chr9:86227400-86227600	Enhancers	Liver	Liver
30	chr9:86227600-86231600	Weak transcription	Liver	Liver
31	chr9:86231600-86233000	Enhancers	Liver	Liver
32	chr9:86233000-86235400	Weak transcription	Liver	Liver
33	chr9:86235400-86235800	Enhancers	Liver	Liver
34	chr9:86235400-86235800	Enhancers	HepG2	liver
35	chr9:86235400-86236000	Enhancers	Duodenum Mucosa	Duodenum
36	chr9:86235400-86236200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr9:86235600-86235800	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr9:86235600-86235800	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr9:86235600-86235800	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
40	chr9:86235600-86235800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr9:86235600-86235800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr9:86235600-86235800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr9:86235600-86235800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr9:86235600-86235800	Enhancers	Rectal Mucosa Donor 29	rectum
45	chr9:86235600-86235800	Enhancers	Osteobl	bone
46	chr9:86235600-86236000	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr9:86235600-86236000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr9:86235600-86236200	Enhancers	H1 Cell Line	embryonic stem cell
49	chr9:86235600-86236200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr9:86235600-86236200	Enhancers	Fetal Heart	heart

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