Variant report

Variant	nsv976316
Chromosome Location	chr14:21702488-21711624
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:21711256-21711587	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:21709409-21709593	HepG2	liver:	n/a	n/a
3	BCLAF1	chr14:21710768-21711305	GM12878	blood:	n/a	n/a
4	BCLAF1	chr14:21706763-21707518	GM12878	blood:	n/a	n/a
5	BCLAF1	chr14:21709359-21711746	GM12878	blood:	n/a	n/a
6	BCLAF1	chr14:21705331-21705994	GM12878	blood:	n/a	n/a
7	BRCA1	chr14:21709394-21709761	Hela-S3	cervix:	n/a	n/a
8	CTCF	chr14:21709500-21709650	AG09319	gingival:	n/a	chr14:21709563-21709581 chr14:21709565-21709586 chr14:21709564-21709580 chr14:21709568-21709576
9	CTCF	chr14:21709360-21709510	RPTEC	kidney:	n/a	n/a
10	CTCF	chr14:21709520-21709670	NB4	blood:	n/a	chr14:21709563-21709581 chr14:21709565-21709586 chr14:21709564-21709580 chr14:21709568-21709576
11	CTCF	chr14:21709220-21709370	HBMEC	blood vessel:	n/a	n/a
12	CTCF	chr14:21709540-21709690	BE2_C	brain:	n/a	chr14:21709563-21709581 chr14:21709565-21709586 chr14:21709564-21709580 chr14:21709568-21709576
13	CTCF	chr14:21709380-21709788	HepG2	liver:	n/a	chr14:21709563-21709581 chr14:21709565-21709586 chr14:21709564-21709580 chr14:21709568-21709576
14	CTCF	chr14:21709520-21709670	HPF	lung:	n/a	chr14:21709563-21709581 chr14:21709565-21709586 chr14:21709564-21709580 chr14:21709568-21709576
15	CTCF	chr14:21709420-21709570	NHLF	lung:	n/a	n/a
16	CTCF	chr14:21709220-21709370	HCT-116	colon:	n/a	n/a
17	CTCF	chr14:21709460-21709610	GM06990	blood:	n/a	chr14:21709563-21709581 chr14:21709565-21709586 chr14:21709564-21709580 chr14:21709568-21709576
18	CTCF	chr14:21709820-21709970	HRPEpiC	eye:	n/a	n/a
19	CTCF	chr14:21709420-21709570	GM12865	blood:	n/a	n/a
20	CTCF	chr14:21709520-21709670	AG04449	skin:	n/a	chr14:21709563-21709581 chr14:21709565-21709586 chr14:21709564-21709580 chr14:21709568-21709576
21	CTCF	chr14:21709440-21709590	HCPEpiC	choroid plexus:	n/a	chr14:21709563-21709581 chr14:21709565-21709586 chr14:21709564-21709580 chr14:21709568-21709576
22	CTCF	chr14:21709460-21709610	SAEC	small airway:	n/a	chr14:21709563-21709581 chr14:21709565-21709586 chr14:21709564-21709580 chr14:21709568-21709576
23	CTCF	chr14:21709480-21709630	AG09319	gingival:	n/a	chr14:21709563-21709581 chr14:21709565-21709586 chr14:21709564-21709580 chr14:21709568-21709576
24	CTCF	chr14:21709480-21709630	AG09309	skin:	n/a	chr14:21709563-21709581 chr14:21709565-21709586 chr14:21709564-21709580 chr14:21709568-21709576
25	CTCF	chr14:21709380-21709530	HMEC	breast:	n/a	n/a
26	CTCF	chr14:21709120-21709270	HFF-Myc	foreskin:	n/a	n/a
27	CTCF	chr14:21709020-21709170	NB4	blood:	n/a	n/a
28	CTCF	chr14:21709460-21709610	AG09309	skin:	n/a	chr14:21709563-21709581 chr14:21709565-21709586 chr14:21709564-21709580 chr14:21709568-21709576
29	CTCF	chr14:21709560-21709710	GM12864	blood:	n/a	chr14:21709563-21709581 chr14:21709565-21709586 chr14:21709564-21709580 chr14:21709568-21709576
30	CTCF	chr14:21709640-21709790	GM12866	blood:	n/a	n/a
31	CTCF	chr14:21709280-21709366	GM19238	blood:	n/a	n/a
32	CTCF	chr14:21709500-21709650	BE2_C	brain:	n/a	chr14:21709563-21709581 chr14:21709565-21709586 chr14:21709564-21709580 chr14:21709568-21709576
33	CTCF	chr14:21709523-21709633	GM13977	blood:	n/a	chr14:21709563-21709581 chr14:21709565-21709586 chr14:21709564-21709580 chr14:21709568-21709576
34	CTCF	chr14:21709520-21709670	HFF-Myc	foreskin:	n/a	chr14:21709563-21709581 chr14:21709565-21709586 chr14:21709564-21709580 chr14:21709568-21709576
35	CTCF	chr14:21709400-21709550	NHDF-neo	bronchial:	n/a	n/a
36	CTCF	chr14:21709271-21709404	ProgFib	skin:	n/a	n/a
37	CTCF	chr14:21709520-21709670	GM12872	blood:	n/a	chr14:21709563-21709581 chr14:21709565-21709586 chr14:21709564-21709580 chr14:21709568-21709576
38	CTCF	chr14:21709100-21709250	GM12871	blood:	n/a	n/a
39	CTCF	chr14:21709460-21709610	HVMF	connective:	n/a	chr14:21709563-21709581 chr14:21709565-21709586 chr14:21709564-21709580 chr14:21709568-21709576
40	CTCF	chr14:21709180-21709330	A549	lung:	n/a	n/a
41	CTCF	chr14:21709340-21709610	GM12873	blood:	n/a	chr14:21709563-21709581 chr14:21709565-21709586 chr14:21709564-21709580 chr14:21709568-21709576
42	CTCF	chr14:21709500-21709650	AG04449	skin:	n/a	chr14:21709563-21709581 chr14:21709565-21709586 chr14:21709564-21709580 chr14:21709568-21709576
43	CTCF	chr14:21709240-21709390	HCPEpiC	choroid plexus:	n/a	n/a
44	CTCF	chr14:21709180-21709330	HepG2	liver:	n/a	n/a
45	CTCF	chr14:21709420-21709570	GM06990	blood:	n/a	n/a
46	CTCF	chr14:21709480-21709630	HCPEpiC	choroid plexus:	n/a	chr14:21709563-21709581 chr14:21709565-21709586 chr14:21709564-21709580 chr14:21709568-21709576
47	CTCF	chr14:21709520-21709670	HL-60	blood:	n/a	chr14:21709563-21709581 chr14:21709565-21709586 chr14:21709564-21709580 chr14:21709568-21709576
48	CTCF	chr14:21709180-21709330	HMEC	breast:	n/a	n/a
49	CTCF	chr14:21709160-21709310	RPTEC	kidney:	n/a	n/a
50	CTCF	chr14:21709180-21709330	GM12867	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:21704611-21704661	NHBE	bronchial:	n/a
2	chr14:21704611-21704661	MCF10A-Er-Src	breast:	n/a
3	chr14:21704611-21704661	HRCEpiC	kidney:	n/a
4	chr14:21704611-21704661	ProgFib	skin:	n/a
5	chr14:21704611-21704661	PANC-1	pancreas:	n/a
6	chr14:21704611-21704661	NT2-D1	testis:	n/a
7	chr14:21704611-21704661	HPAEpiC	pulmonary alveolar:	n/a
8	chr14:21704611-21704661	PrEC	prostate:	n/a
9	chr14:21704611-21704661	SK-N-SH_RA	brain:	n/a
10	chr14:21704611-21704661	AG09309	skin:	n/a
11	chr14:21704611-21704661	Jurkat	blood:	n/a
12	chr14:21704611-21704661	NB4	blood:	n/a
13	chr14:21704611-21704661	Hepatocyte	liver:	n/a
14	chr14:21704611-21704661	T-47D	breast:	n/a
15	chr14:21704611-21704661	LNCaP	prostate:	n/a
16	chr14:21704611-21704661	H1-hESC	embryonic stem cell:	embryo
17	chr14:21704611-21704661	SKMC	muscle:	n/a
18	chr14:21704611-21704661	Hela-S3	cervix:	n/a
19	chr14:21704611-21704661	SAEC	small airway:	n/a
20	chr14:21704611-21704661	BE2_C	brain:	n/a
21	chr14:21704611-21704661	MCF-7	breast:	n/a
22	chr14:21704611-21704661	HMEC	breast:	n/a
23	chr14:21704611-21704661	AG10803	skin:	n/a
24	chr14:21704611-21704661	HNPCEpiC	eye:	n/a
25	chr14:21704611-21704661	HepG2	liver:	n/a
26	chr14:21704611-21704661	NH-A	brain:	n/a
27	chr14:21704611-21704661	HIPEpiC	eye:	n/a
28	chr14:21704611-21704661	HCPEpiC	choroid plexus:	n/a
29	chr14:21704611-21704661	HL-60	blood:	n/a
30	chr14:21704611-21704661	IMR90	lung:	fetal
31	chr14:21704611-21704661	HCT-116	colon:	n/a
32	chr14:21704611-21704661	PFSK-1	brain:	n/a
33	chr14:21704611-21704661	U87	brain:	n/a
34	chr14:21704611-21704661	SK-N-SH	brain:	n/a
35	chr14:21704611-21704661	HCF	heart:	n/a
36	chr14:21704611-21704661	BJ	skin:	n/a
37	chr14:21704611-21704661	NHDF-neo	bronchial:	n/a
38	chr14:21704611-21704661	HEK293	kidney:	embryo
39	chr14:21704611-21704661	AG09319	gingival:	n/a
40	chr14:21704611-21704661	AG04450	lung:	fetal
41	chr14:21704611-21704661	GM12892	blood:	n/a
42	chr14:21704611-21704661	CMK	blood:	n/a
43	chr14:21704611-21704661	HAEpiC	amniotic membrane:	n/a
44	chr14:21704611-21704661	HRPEpiC	eye:	n/a
45	chr14:21704611-21704661	AoSMC	blood vessel:	n/a
46	chr14:21704611-21704661	ovcar-3	ovarian:	n/a
47	chr14:21704611-21704661	A549	lung:	n/a
48	chr14:21704611-21704661	GM12878	blood:	n/a
49	chr14:21704611-21704661	GM12891	blood:	n/a
50	chr14:21704611-21704661	HUVEC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:21704009..21707025-chr14:21707040..21709471,4	MCF-7	breast:
2	chr14:21707926..21709527-chr14:21851833..21853917,2	MCF-7	breast:
3	chr14:21703629..21706503-chr14:21849764..21851749,2	MCF-7	breast:
4	chr14:21709944..21712875-chr14:21904000..21906310,2	MCF-7	breast:
5	chr14:21708563..21711469-chr14:21841010..21843260,2	K562	blood:
6	chr14:21705854..21707392-chr14:21708475..21711254,2	K562	blood:
7	chr14:21709759..21712361-chr14:21720311..21725270,5	K562	blood:
8	chr14:21708836..21711408-chr14:21737080..21738669,2	MCF-7	breast:
9	chr14:21702039..21704805-chr14:21710008..21711834,2	MCF-7	breast:
10	chr14:21670001..21672457-chr14:21706378..21709017,2	K562	blood:
11	chr14:21710343..21712000-chr14:21723234..21724761,2	MCF-7	breast:
12	chr14:21704009..21707025-chr14:21707040..21709471,4	MCF-7	breast:
13	chr14:21690598..21692490-chr14:21705492..21708066,2	MCF-7	breast:
14	chr14:21702039..21704805-chr14:21710008..21711834,2	MCF-7	breast:
15	chr14:21701373..21707828-chr14:21708039..21714266,10	K562	blood:
16	chr14:21704014..21706045-chr14:21718733..21720971,2	K562	blood:
17	chr14:21678845..21680444-chr14:21704444..21707261,2	K562	blood:
18	chr14:21709578..21711363-chr14:21732079..21734857,2	MCF-7	breast:
19	chr14:21708482..21710752-chr14:21732706..21735405,2	MCF-7	breast:
20	chr14:21709126..21711410-chr14:21715324..21718061,2	MCF-7	breast:
21	chr14:21707431..21709141-chr14:21735831..21737898,2	K562	blood:
22	chr14:21705289..21706946-chr14:21709944..21711637,2	MCF-7	breast:
23	chr14:21711515..21716714-chr14:21717085..21720110,6	K562	blood:
24	chr14:21702152..21704976-chr14:21712747..21715545,2	MCF-7	breast:
25	chr14:21698449..21701323-chr14:21702052..21705538,3	MCF-7	breast:
26	chr14:21705854..21707392-chr14:21708475..21711254,2	K562	blood:
27	chr14:21694684..21697867-chr14:21700846..21706348,4	MCF-7	breast:
28	chr14:21700872..21703141-chr14:21723886..21726612,2	K562	blood:
29	chr14:21701295..21703897-chr14:21842847..21844816,2	K562	blood:
30	chr14:21705289..21706946-chr14:21709944..21711637,2	MCF-7	breast:
31	chr14:21709277..21713584-chr14:21714708..21717034,3	K562	blood:
32	chr14:21701373..21707828-chr14:21708039..21714266,10	K562	blood:

Variant related genes	Relation type
HNRNPC	TF binding region
HNRNPC	CpG island
ENSG00000260830	chromatin interactions
ENSG00000100888	chromatin interactions
ENSG00000092199	chromatin interactions
ENSG00000092201	chromatin interactions

Extended variants
information (count: 404 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:404 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs185219488	chr14:21702528-21702529	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs549829099	chr14:21702531-21702532	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs200122070	chr14:21702634-21702635	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs35131476	chr14:21702650-21702651	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs569924370	chr14:21702674-21702675	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs535605611	chr14:21702692-21702693	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs145240275	chr14:21702797-21702798	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs531109715	chr14:21702815-21702816	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs549637145	chr14:21702816-21702817	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs150582024	chr14:21702819-21702820	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs139636395	chr14:21702826-21702827	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs570318413	chr14:21702830-21702831	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs571314958	chr14:21702841-21702842	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs539550257	chr14:21702843-21702844	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs556250819	chr14:21702849-21702850	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs190047120	chr14:21702890-21702891	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs191678574	chr14:21702939-21702940	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs555254189	chr14:21702946-21702947	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs367912354	chr14:21702962-21702963	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs11850109	chr14:21702971-21702972	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs539249508	chr14:21702983-21702984	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs11269714	chr14:21703001-21703002	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs201763769	chr14:21703003-21703004	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs371864137	chr14:21703034-21703035	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs377362104	chr14:21703075-21703076	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs370415448	chr14:21703091-21703092	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs4982433	chr14:21703122-21703123	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs533115544	chr14:21703159-21703160	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs117165820	chr14:21703190-21703191	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs559022515	chr14:21703203-21703204	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs34098157	chr14:21703221-21703222	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs74467633	chr14:21703232-21703233	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs184215107	chr14:21703250-21703251	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs569329569	chr14:21703309-21703310	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs566114129	chr14:21703318-21703319	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs528797560	chr14:21703334-21703335	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs367632314	chr14:21703368-21703369	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs565641064	chr14:21703375-21703376	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs536114044	chr14:21703406-21703407	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs149663213	chr14:21703412-21703413	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs4981367	chr14:21703444-21703445	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs8009479	chr14:21703464-21703465	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs150831362	chr14:21703469-21703470	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs376640622	chr14:21703471-21703472	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs551656101	chr14:21703508-21703509	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs538267110	chr14:21703537-21703538	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs145483102	chr14:21703549-21703550	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs556188062	chr14:21703567-21703568	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs17102712	chr14:21703589-21703590	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs535519110	chr14:21703622-21703623	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Cancer	20164920	CNVD
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cone-rod dystrophy	18421352	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myelofibrosis	22110671	CNVD
Alzheimer''s disease	21482944	CNVD
Mental retardation	19951919	CNVD
Neuroblastoma	21899760	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Heart disease	21282601	CNVD
Esophageal cancer	20955586	CNVD
Neurodevelopmental disorder	22521361	CNVD
Lung cancer	16773561	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17440070	CNVD
Breast cancer	16272173	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
severe speech impairment	20736978	CNVD
speech impairment	20736978	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
Cancer	20164919	CNVD
Breast cancer	21364760	CNVD
Mortal	21835882	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	21858162	CNVD
Schizophrenia	20967226	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Autism	22102821	CNVD
Neuroblastoma	19536264	CNVD
Schizophrenia	23813976	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Ewing''s sarcoma	18628472	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:21671200-21732000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr14:21672400-21709000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr14:21672600-21703000	Strong transcription	Primary neutrophils fromperipheralblood	blood
4	chr14:21672800-21709000	Strong transcription	Monocytes-CD14+_RO01746	blood
5	chr14:21672800-21725200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
6	chr14:21673000-21702600	Strong transcription	Cortex derived primary cultured neurospheres	brain
7	chr14:21673000-21702800	Strong transcription	Fetal Intestine Large	intestine
8	chr14:21673200-21709200	Strong transcription	Primary monocytes fromperipheralblood	blood
9	chr14:21673600-21706000	Strong transcription	Rectal Mucosa Donor 31	rectum
10	chr14:21677800-21727000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
11	chr14:21681000-21714000	Strong transcription	H1 Cell Line	embryonic stem cell
12	chr14:21682400-21703400	Strong transcription	Fetal Muscle Leg	muscle
13	chr14:21684000-21702600	Strong transcription	Sigmoid Colon	Sigmoid Colon
14	chr14:21684400-21705200	Strong transcription	Primary B cells from peripheral blood	blood
15	chr14:21685800-21703400	Strong transcription	GM12878-XiMat	blood
16	chr14:21686200-21702600	Strong transcription	H9 Cell Line	embryonic stem cell
17	chr14:21686400-21704400	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr14:21687600-21706400	Strong transcription	HUES48 Cell Line	embryonic stem cell
19	chr14:21687600-21723200	Strong transcription	HUES64 Cell Line	embryonic stem cell
20	chr14:21688200-21712800	Strong transcription	HMEC	breast
21	chr14:21688200-21725200	Strong transcription	HUES6 Cell Line	embryonic stem cell
22	chr14:21688400-21704200	Strong transcription	HSMM	muscle
23	chr14:21688400-21712800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr14:21688600-21707000	Strong transcription	Placenta	Placenta
25	chr14:21689000-21702600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr14:21689400-21703400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr14:21689600-21704600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
28	chr14:21689600-21723800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr14:21689600-21725000	Strong transcription	NHEK	skin
30	chr14:21689800-21709200	Strong transcription	Hela-S3	cervix
31	chr14:21689800-21716200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr14:21690000-21703000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr14:21690200-21705600	Weak transcription	Small Intestine	intestine
34	chr14:21691400-21703800	Strong transcription	HepG2	liver
35	chr14:21691600-21704600	Strong transcription	HUVEC	blood vessel
36	chr14:21692000-21703000	Strong transcription	HSMMtube	muscle
37	chr14:21692000-21730600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr14:21692200-21702800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr14:21693000-21704200	Strong transcription	NH-A	brain
40	chr14:21693800-21702800	Strong transcription	Placenta Amnion	Placenta Amnion
41	chr14:21694400-21705600	Weak transcription	Aorta	Aorta
42	chr14:21694800-21702600	Genic enhancers	Primary T helper naive cells fromperipheralblood	blood
43	chr14:21695000-21711600	Genic enhancers	Primary T helper cells fromperipheralblood	blood
44	chr14:21696400-21718400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr14:21697400-21704800	Strong transcription	NHDF-Ad	bronchial
46	chr14:21697400-21705600	Genic enhancers	Primary T killer memory cells from peripheral blood	blood
47	chr14:21697400-21708000	Strong transcription	Primary hematopoietic stem cells	blood
48	chr14:21697600-21716400	Strong transcription	K562	blood
49	chr14:21698000-21712600	Strong transcription	Primary B cells from cord blood	blood
50	chr14:21698000-21718000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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