Variant report

Variant	nsv831408
Chromosome Location	chr8:100523523-100721507
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1058)
CpG islands
(count:611)
Chromatin interactive
region (count:86)
LncRNA
region (count:1)
Mature miRNA
region (count: 3)
miRNA target
sites (count:0)

(count:1058 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:100694633-100695046	K562	blood:	n/a	n/a
2	ARID3A	chr8:100649546-100649965	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:100718258-100718424	K562	blood:	n/a	chr8:100718324-100718340
4	ARID3A	chr8:100645951-100646742	HepG2	liver:	n/a	chr8:100645997-100646013
5	ARID3A	chr8:100649502-100649902	K562	blood:	n/a	n/a
6	ATF1	chr8:100609763-100609906	K562	blood:	n/a	n/a
7	ATF1	chr8:100617407-100617536	K562	blood:	n/a	n/a
8	ATF1	chr8:100649659-100649974	K562	blood:	n/a	n/a
9	ATF1	chr8:100654398-100654716	K562	blood:	n/a	n/a
10	ATF1	chr8:100718057-100718285	K562	blood:	n/a	n/a
11	ATF2	chr8:100675713-100676177	GM12878	blood:	n/a	n/a
12	ATF2	chr8:100675640-100676176	GM12878	blood:	n/a	n/a
13	ATF2	chr8:100667670-100668603	GM12878	blood:	n/a	n/a
14	ATF3	chr8:100717996-100718348	K562	blood:	n/a	n/a
15	BACH1	chr8:100721411-100721526	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr8:100694808-100695067	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr8:100694604-100695056	K562	blood:	n/a	n/a
18	BATF	chr8:100667761-100668621	GM12878	blood:	n/a	n/a
19	BATF	chr8:100692484-100692710	GM12878	blood:	n/a	n/a
20	BATF	chr8:100668748-100669124	GM12878	blood:	n/a	n/a
21	BATF	chr8:100698390-100698700	GM12878	blood:	n/a	chr8:100698530-100698541
22	BATF	chr8:100694712-100695127	GM12878	blood:	n/a	chr8:100694911-100694922
23	BATF	chr8:100648147-100648397	GM12878	blood:	n/a	n/a
24	BATF	chr8:100694790-100695087	GM12878	blood:	n/a	chr8:100694911-100694922
25	BATF	chr8:100667811-100668195	GM12878	blood:	n/a	n/a
26	BATF	chr8:100691641-100691903	GM12878	blood:	n/a	n/a
27	BATF	chr8:100668709-100669157	GM12878	blood:	n/a	n/a
28	BHLHE40	chr8:100718090-100718272	K562	blood:	n/a	n/a
29	BHLHE40	chr8:100694837-100695113	K562	blood:	n/a	n/a
30	BHLHE40	chr8:100675664-100676151	GM12878	blood:	n/a	n/a
31	BHLHE40	chr8:100694838-100695063	GM12878	blood:	n/a	n/a
32	BHLHE40	chr8:100667840-100667899	A549	lung:	n/a	n/a
33	BHLHE40	chr8:100649672-100649953	K562	blood:	n/a	n/a
34	CBX3	chr8:100697546-100698225	K562	blood:	n/a	n/a
35	CBX3	chr8:100694702-100695193	K562	blood:	n/a	n/a
36	CBX3	chr8:100597517-100597878	K562	blood:	n/a	n/a
37	CBX3	chr8:100697629-100697987	K562	blood:	n/a	n/a
38	CCNT2	chr8:100649652-100649903	K562	blood:	n/a	n/a
39	CEBPB	chr8:100636676-100636928	HepG2	liver:	n/a	n/a
40	CEBPB	chr8:100529828-100530011	A549	lung:	n/a	chr8:100529878-100529889
41	CEBPB	chr8:100606676-100607259	HepG2	liver:	n/a	chr8:100606832-100606843 chr8:100606795-100606806
42	CEBPB	chr8:100675718-100676141	ECC-1	luminal epithelium:	n/a	n/a
43	CEBPB	chr8:100668144-100669367	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr8:100526518-100526745	A549	lung:	n/a	chr8:100526596-100526607
45	CEBPB	chr8:100526454-100526740	HepG2	liver:	n/a	chr8:100526596-100526607
46	CEBPB	chr8:100526459-100526773	K562	blood:	n/a	chr8:100526596-100526607
47	CEBPB	chr8:100595818-100596124	ECC-1	luminal epithelium:	n/a	chr8:100595943-100595952 chr8:100595943-100595952 chr8:100595941-100595954 chr8:100595943-100595952 chr8:100595941-100595952
48	CEBPB	chr8:100540080-100540378	K562	blood:	n/a	chr8:100540222-100540235 chr8:100540223-100540234 chr8:100540224-100540233 chr8:100540222-100540233 chr8:100540222-100540235
49	CEBPB	chr8:100716555-100716911	Hela-S3	cervix:	n/a	chr8:100716732-100716743
50	CEBPB	chr8:100595766-100596138	H1-hESC	embryonic stem cell:	n/a	chr8:100595943-100595952 chr8:100595943-100595952 chr8:100595941-100595954 chr8:100595943-100595952 chr8:100595941-100595952

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:100549849-100549899	GM12878	blood:	n/a
2	chr8:100549849-100549899	GM12878	blood:	n/a
3	chr8:100708621-100708671	GM12892	blood:	n/a
4	chr8:100549849-100549899	ovcar-3	ovarian:	n/a
5	chr8:100635039-100635089	HepG2	liver:	n/a
6	chr8:100708945-100708995	HNPCEpiC	eye:	n/a
7	chr8:100649114-100649164	AG04450	lung:	fetal
8	chr8:100559503-100559553	HIPEpiC	eye:	n/a
9	chr8:100549849-100549899	MCF10A-Er-Src	breast:	n/a
10	chr8:100549776-100549826	HRPEpiC	eye:	n/a
11	chr8:100708545-100708595	HCT-116	colon:	n/a
12	chr8:100549776-100549826	Caco-2	colon:	n/a
13	chr8:100649114-100649164	BJ	skin:	n/a
14	chr8:100649114-100649164	AoSMC	blood vessel:	n/a
15	chr8:100716071-100716121	AoSMC	blood vessel:	n/a
16	chr8:100708945-100708995	AG04450	lung:	fetal
17	chr8:100649114-100649164	ovcar-3	ovarian:	n/a
18	chr8:100708621-100708671	HCT-116	colon:	n/a
19	chr8:100708545-100708595	HEEpiC	esophagus:	n/a
20	chr8:100649114-100649164	HEEpiC	esophagus:	n/a
21	chr8:100559503-100559553	GM12878	blood:	n/a
22	chr8:100635039-100635089	HCM	heart:	n/a
23	chr8:100549776-100549826	HCM	heart:	n/a
24	chr8:100708945-100708995	GM12892	blood:	n/a
25	chr8:100549849-100549899	AG09309	skin:	n/a
26	chr8:100559503-100559553	SKMC	muscle:	n/a
27	chr8:100708945-100708995	HRPEpiC	eye:	n/a
28	chr8:100549849-100549899	NH-A	brain:	n/a
29	chr8:100549849-100549899	T-47D	breast:	n/a
30	chr8:100667796-100667846	HRCEpiC	kidney:	n/a
31	chr8:100708621-100708671	HRPEpiC	eye:	n/a
32	chr8:100708621-100708671	SK-N-MC	brain:	n/a
33	chr8:100649114-100649164	AG04449	skin:	fetal
34	chr8:100667796-100667846	PANC-1	pancreas:	n/a
35	chr8:100708545-100708595	AG04449	skin:	fetal
36	chr8:100635039-100635089	SKMC	muscle:	n/a
37	chr8:100635039-100635089	GM19239	blood:	n/a
38	chr8:100708545-100708595	HCF	heart:	n/a
39	chr8:100635039-100635089	AoSMC	blood vessel:	n/a
40	chr8:100708545-100708595	U87	brain:	n/a
41	chr8:100716071-100716121	GM12878	blood:	n/a
42	chr8:100708945-100708995	HPAEpiC	pulmonary alveolar:	n/a
43	chr8:100559503-100559553	SK-N-SH	brain:	n/a
44	chr8:100549849-100549899	SK-N-MC	brain:	n/a
45	chr8:100708945-100708995	HAEpiC	amniotic membrane:	n/a
46	chr8:100667796-100667846	BJ	skin:	n/a
47	chr8:100708621-100708671	HL-60	blood:	n/a
48	chr8:100667796-100667846	ProgFib	skin:	n/a
49	chr8:100549849-100549899	AoSMC	blood vessel:	n/a
50	chr8:100708621-100708671	NH-A	brain:	n/a

(count:86 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:100550054..100551658-chr8:100559009..100560949,2	K562	blood:
2	chr8:100683905..100686290-chr8:100687390..100689544,2	MCF-7	breast:
3	chr8:100684752..100688418-chr8:100691924..100694879,3	K562	blood:
4	chr8:100683905..100686290-chr8:100687390..100689544,2	MCF-7	breast:
5	chr8:100403774..100404566-chr8:100616940..100617627,2	MCF-7	breast:
6	chr8:100587220..100589733-chr8:100589949..100592234,2	K562	blood:
7	chr8:100708369..100711314-chr8:100713303..100715085,2	MCF-7	breast:
8	chr8:100415595..100418351-chr8:100620634..100623512,2	MCF-7	breast:
9	chr8:100578110..100580949-chr8:100589629..100591641,2	MCF-7	breast:
10	chr8:100558486..100560693-chr8:100576849..100579778,3	MCF-7	breast:
11	chr8:100550054..100551658-chr8:100559009..100560949,2	K562	blood:
12	chr8:100684752..100688418-chr8:100691924..100694879,3	K562	blood:
13	chr8:100553009..100554706-chr8:100561096..100563189,2	K562	blood:
14	chr8:100607378..100609807-chr8:100619167..100621147,2	K562	blood:
15	chr8:100629647..100631528-chr8:100671490..100673021,2	K562	blood:
16	chr8:100607857..100609807-chr8:100619167..100621104,2	K562	blood:
17	chr8:100588643..100590809-chr8:100667230..100669836,2	MCF-7	breast:
18	chr8:100662125..100664863-chr8:100667158..100669715,2	MCF-7	breast:
19	chr8:100641638..100644745-chr8:100644767..100647893,3	K562	blood:
20	chr8:100525847..100527559-chr8:100529820..100532768,2	MCF-7	breast:
21	chr8:100544046..100548556-chr8:100548656..100552103,4	K562	blood:
22	chr8:100719725..100721462-chr8:100723554..100725582,2	K562	blood:
23	chr8:100637655..100639702-chr8:100646117..100648663,2	MCF-7	breast:
24	chr8:100525847..100527559-chr8:100529820..100532768,2	MCF-7	breast:
25	chr8:100666079..100668727-chr8:100674262..100677111,3	K562	blood:
26	chr8:100693440..100695370-chr8:100718101..100720996,2	K562	blood:
27	chr8:100558748..100564214-chr8:100565274..100568136,5	MCF-7	breast:
28	chr8:100715387..100717513-chr8:100719961..100722930,2	K562	blood:
29	chr8:100534887..100536607-chr8:100537446..100539997,2	K562	blood:
30	chr8:100662125..100664863-chr8:100667158..100669715,2	MCF-7	breast:
31	chr8:100715769..100720445-chr8:100721674..100725414,4	MCF-7	breast:
32	chr8:100553009..100554706-chr8:100561096..100563189,2	K562	blood:
33	chr8:100634441..100637349-chr8:100638779..100641653,3	K562	blood:
34	chr5:179049397..179051041-chr8:100524000..100525807,2	MCF-7	breast:
35	chr8:100634973..100637054-chr8:100640847..100642958,2	MCF-7	breast:
36	chr8:100712738..100714435-chr8:100716061..100717614,2	K562	blood:
37	chr8:100532719..100535105-chr8:100539628..100541847,3	MCF-7	breast:
38	chr8:100651536..100655023-chr8:100656332..100658879,3	K562	blood:
39	chr8:100539051..100543758-chr8:100545879..100549609,5	K562	blood:
40	chr8:100634441..100637349-chr8:100638779..100641653,3	K562	blood:
41	chr8:100651536..100655023-chr8:100656332..100658879,3	K562	blood:
42	chr8:100708369..100711314-chr8:100713303..100715085,2	MCF-7	breast:
43	chr8:100707994..100711279-chr8:100711487..100714977,4	K562	blood:
44	chr8:100607857..100609807-chr8:100619167..100621104,2	K562	blood:
45	chr8:100652613..100655160-chr8:100773640..100775434,2	K562	blood:
46	chr8:100700326..100701994-chr8:100715274..100717581,2	K562	blood:
47	chr8:100693440..100695370-chr8:100718101..100720996,2	K562	blood:
48	chr8:100693782..100695662-chr8:100781246..100783612,2	K562	blood:
49	chr8:100588643..100590809-chr8:100667230..100669836,2	MCF-7	breast:
50	chr8:100560158..100563558-chr8:100564572..100567827,4	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-COX6C-2	chr8:100626014-100626306	NONHSAT127958

miRNA name	Chromosome Location	mirBase accession
hsa-miR-599	chr8:100548879-100548898	MIMAT0003267
hsa-miR-875-5p	chr8:100549058-100549079	MIMAT0004922
hsa-miR-875-3p	chr8:100549025-100549045	MIMAT0004923

No data

Variant related genes	Relation type
RN7SL350P	TF binding region
VPS13B	TF binding region
ENSG00000206699	TF binding region
MIR599	TF binding region
MIR875	TF binding region
ENSG00000235683	TF binding region
RN7SL350P	CpG island
VPS13B	CpG island
ENSG00000206699	CpG island
MIR599	CpG island
MIR875	CpG island
ENSG00000235683	CpG island
ENSG00000216069	chromatin interactions
ENSG00000132549	chromatin interactions
ENSG00000235683	chromatin interactions
ENSG00000169045	chromatin interactions
ENSG00000207804	chromatin interactions
ENSG00000243254	chromatin interactions
ENSG00000206699	chromatin interactions

Extended variants
information (count: 6579 )
Associated
traits (count: 110 )

Variant overlapped rSNPs/rCNVs (count:6579 , 50 per page) page: 1 2 3 4 5 6 7 ... 132

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs148033080	chr8:100523559-100523560	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs370519991	chr8:100523563-100523564	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs373919780	chr8:100523569-100523570	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs538237107	chr8:100523599-100523600	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs386834089	chr8:100523604-100523605	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs140797231	chr8:100523624-100523625	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs558460255	chr8:100523641-100523642	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs375652507	chr8:100523656-100523657	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs531149269	chr8:100523657-100523658	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs150376603	chr8:100523658-100523659	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs200774003	chr8:100523677-100523678	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs200815297	chr8:100523704-100523705	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs552843068	chr8:100523729-100523730	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs370741245	chr8:100523765-100523766	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs117661187	chr8:100523793-100523794	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs564668928	chr8:100523807-100523808	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs533608381	chr8:100523808-100523809	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs547101804	chr8:100523882-100523883	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs374740400	chr8:100523883-100523884	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs566999624	chr8:100523900-100523901	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs185137371	chr8:100523941-100523942	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs189937894	chr8:100523962-100523963	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs569017636	chr8:100523997-100523998	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs16897410	chr8:100524042-100524043	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs6998028	chr8:100524075-100524076	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs577404847	chr8:100524090-100524091	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs533771589	chr8:100524094-100524095	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs575118145	chr8:100524122-100524123	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs182552365	chr8:100524166-100524167	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs574512457	chr8:100524290-100524291	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs36091732	chr8:100524298-100524299	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs542221145	chr8:100524324-100524325	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs186710721	chr8:100524332-100524333	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs576003479	chr8:100524400-100524401	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs544882845	chr8:100524455-100524456	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs3134171	chr8:100524572-100524573	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs191496925	chr8:100524608-100524609	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs371787112	chr8:100524648-100524649	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs563608947	chr8:100524654-100524655	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs547238363	chr8:100524692-100524693	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs560536807	chr8:100524712-100524713	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs183844514	chr8:100524715-100524716	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs188732408	chr8:100524730-100524731	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs569231276	chr8:100524736-100524737	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs537891793	chr8:100524758-100524759	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs192337288	chr8:100524760-100524761	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs183244109	chr8:100524819-100524820	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs533707992	chr8:100524961-100524962	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs186554555	chr8:100525013-100525014	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs573358488	chr8:100525081-100525082	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:110)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Multiple myeloma	16461302	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
small cell lung cancer	20016488	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	17260012	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Colorectal cancer	19455253	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	21611746	CNVD
Cohen syndrome	20461111	CNVD
Prostate cancer	22341455	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
T-cell lymphomas	22341440	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:2064 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:100473400-100526000	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr8:100491200-100537000	Weak transcription	Placenta	Placenta
3	chr8:100495200-100532600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr8:100496400-100537200	Weak transcription	Brain Hippocampus Middle	brain
5	chr8:100499400-100535200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
6	chr8:100503800-100536600	Weak transcription	Fetal Muscle Leg	muscle
7	chr8:100505000-100534800	Weak transcription	Fetal Intestine Large	intestine
8	chr8:100505200-100525000	Weak transcription	Stomach Smooth Muscle	stomach
9	chr8:100505200-100532400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr8:100506000-100535400	Weak transcription	Fetal Stomach	stomach
11	chr8:100508400-100535400	Weak transcription	Aorta	Aorta
12	chr8:100508400-100535400	Weak transcription	Right Ventricle	heart
13	chr8:100508400-100535600	Weak transcription	Pancreas	Pancrea
14	chr8:100508400-100538400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr8:100508400-100574000	Weak transcription	Gastric	stomach
16	chr8:100511200-100523800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr8:100511200-100524000	Weak transcription	Psoas Muscle	Psoas
18	chr8:100511200-100538400	Weak transcription	Sigmoid Colon	Sigmoid Colon
19	chr8:100511600-100524000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
20	chr8:100511600-100533000	Weak transcription	Dnd41	blood
21	chr8:100511600-100535400	Weak transcription	Ovary	ovary
22	chr8:100511600-100559400	Weak transcription	Rectal Mucosa Donor 31	rectum
23	chr8:100511800-100533000	Weak transcription	HSMM	muscle
24	chr8:100511800-100539000	Weak transcription	Liver	Liver
25	chr8:100512000-100525200	Weak transcription	NHLF	lung
26	chr8:100512000-100535400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
27	chr8:100512200-100526600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr8:100512200-100534200	Weak transcription	NH-A	brain
29	chr8:100512200-100534800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
30	chr8:100512200-100538400	Weak transcription	Fetal Intestine Small	intestine
31	chr8:100512200-100545800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
32	chr8:100512200-100549800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
33	chr8:100512200-100557400	Weak transcription	Duodenum Mucosa	Duodenum
34	chr8:100512200-100559400	Weak transcription	Small Intestine	intestine
35	chr8:100512400-100524600	Weak transcription	Primary T helper cells PMA-I stimulated	--
36	chr8:100512400-100533000	Weak transcription	Primary monocytes fromperipheralblood	blood
37	chr8:100512400-100535400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr8:100512400-100545800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr8:100512600-100533000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
40	chr8:100512600-100533200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr8:100512600-100537400	Weak transcription	Brain Substantia Nigra	brain
42	chr8:100513200-100535400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr8:100513600-100528600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr8:100514400-100535400	Weak transcription	Lung	lung
45	chr8:100515800-100533200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr8:100516000-100526600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr8:100516200-100533400	Weak transcription	NHDF-Ad	bronchial
48	chr8:100516400-100589000	Weak transcription	Primary T cells fromperipheralblood	blood
49	chr8:100516600-100533200	Weak transcription	Adipose Nuclei	Adipose
50	chr8:100516800-100533200	Weak transcription	Primary hematopoietic stem cells	blood

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