Variant report

Variant	nsv891227
Chromosome Location	chr8:100295634-100743556
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2680)
CpG islands
(count:854)
Chromatin interactive
region (count:195)
LncRNA
region (count:8)
Mature miRNA
region (count: 3)
miRNA target
sites (count:0)

(count:2680 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:100476490-100476616	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:100718258-100718424	K562	blood:	n/a	chr8:100718324-100718340
3	ARID3A	chr8:100649546-100649965	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:100510905-100511524	HepG2	liver:	n/a	n/a
5	ARID3A	chr8:100519158-100519359	HepG2	liver:	n/a	n/a
6	ARID3A	chr8:100400144-100400181	K562	blood:	n/a	n/a
7	ARID3A	chr8:100370860-100371168	K562	blood:	n/a	n/a
8	ARID3A	chr8:100370824-100371122	HepG2	liver:	n/a	n/a
9	ARID3A	chr8:100694633-100695046	K562	blood:	n/a	n/a
10	ARID3A	chr8:100416524-100416817	K562	blood:	n/a	n/a
11	ARID3A	chr8:100649502-100649902	K562	blood:	n/a	n/a
12	ARID3A	chr8:100645951-100646742	HepG2	liver:	n/a	chr8:100645997-100646013
13	ARID3A	chr8:100298952-100299271	HepG2	liver:	n/a	n/a
14	ARID3A	chr8:100445541-100445734	HepG2	liver:	n/a	n/a
15	ATF1	chr8:100649659-100649974	K562	blood:	n/a	n/a
16	ATF1	chr8:100718057-100718285	K562	blood:	n/a	n/a
17	ATF1	chr8:100468108-100468135	K562	blood:	n/a	n/a
18	ATF1	chr8:100654398-100654716	K562	blood:	n/a	n/a
19	ATF1	chr8:100515482-100515487	K562	blood:	n/a	n/a
20	ATF1	chr8:100416505-100416787	K562	blood:	n/a	n/a
21	ATF1	chr8:100609763-100609906	K562	blood:	n/a	n/a
22	ATF1	chr8:100370807-100371120	K562	blood:	n/a	n/a
23	ATF1	chr8:100617407-100617536	K562	blood:	n/a	n/a
24	ATF2	chr8:100667670-100668603	GM12878	blood:	n/a	n/a
25	ATF2	chr8:100675640-100676176	GM12878	blood:	n/a	n/a
26	ATF2	chr8:100675713-100676177	GM12878	blood:	n/a	n/a
27	ATF3	chr8:100717996-100718348	K562	blood:	n/a	n/a
28	BACH1	chr8:100721411-100721526	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr8:100740215-100740602	K562	blood:	n/a	n/a
30	BACH1	chr8:100389266-100389270	K562	blood:	n/a	n/a
31	BACH1	chr8:100395401-100395488	K562	blood:	n/a	n/a
32	BACH1	chr8:100694808-100695067	H1-hESC	embryonic stem cell:	n/a	n/a
33	BACH1	chr8:100694604-100695056	K562	blood:	n/a	n/a
34	BACH1	chr8:100740225-100740473	H1-hESC	embryonic stem cell:	n/a	n/a
35	BATF	chr8:100460738-100460975	GM12878	blood:	n/a	chr8:100460813-100460824
36	BATF	chr8:100668748-100669124	GM12878	blood:	n/a	n/a
37	BATF	chr8:100510819-100511214	GM12878	blood:	n/a	chr8:100510967-100510978
38	BATF	chr8:100510858-100511111	GM12878	blood:	n/a	chr8:100510967-100510978
39	BATF	chr8:100507953-100508207	GM12878	blood:	n/a	n/a
40	BATF	chr8:100692484-100692710	GM12878	blood:	n/a	n/a
41	BATF	chr8:100508028-100508205	GM12878	blood:	n/a	n/a
42	BATF	chr8:100698390-100698700	GM12878	blood:	n/a	chr8:100698530-100698541
43	BATF	chr8:100694712-100695127	GM12878	blood:	n/a	chr8:100694911-100694922
44	BATF	chr8:100667811-100668195	GM12878	blood:	n/a	n/a
45	BATF	chr8:100648147-100648397	GM12878	blood:	n/a	n/a
46	BATF	chr8:100667761-100668621	GM12878	blood:	n/a	n/a
47	BATF	chr8:100460709-100460986	GM12878	blood:	n/a	chr8:100460813-100460824
48	BATF	chr8:100694790-100695087	GM12878	blood:	n/a	chr8:100694911-100694922
49	BATF	chr8:100668709-100669157	GM12878	blood:	n/a	n/a
50	BATF	chr8:100691641-100691903	GM12878	blood:	n/a	n/a

(count:854 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:100549849-100549899	HRCEpiC	kidney:	n/a
2	chr8:100493491-100493541	A549	lung:	n/a
3	chr8:100297748-100297798	A549	lung:	n/a
4	chr8:100493491-100493541	PrEC	prostate:	n/a
5	chr8:100464878-100464928	GM06990	blood:	n/a
6	chr8:100297748-100297798	AG10803	skin:	n/a
7	chr8:100708545-100708595	Hela-S3	cervix:	n/a
8	chr8:100549849-100549899	HCF	heart:	n/a
9	chr8:100708545-100708595	Jurkat	blood:	n/a
10	chr8:100716071-100716121	NHBE	bronchial:	n/a
11	chr8:100708945-100708995	HCM	heart:	n/a
12	chr8:100549776-100549826	HL-60	blood:	n/a
13	chr8:100549776-100549826	CMK	blood:	n/a
14	chr8:100667796-100667846	Jurkat	blood:	n/a
15	chr8:100649114-100649164	PFSK-1	brain:	n/a
16	chr8:100334620-100334670	HCPEpiC	choroid plexus:	n/a
17	chr8:100708621-100708671	HNPCEpiC	eye:	n/a
18	chr8:100635039-100635089	NB4	blood:	n/a
19	chr8:100649114-100649164	SAEC	small airway:	n/a
20	chr8:100635039-100635089	LNCaP	prostate:	n/a
21	chr8:100297748-100297798	AG09309	skin:	n/a
22	chr8:100708621-100708671	IMR90	lung:	fetal
23	chr8:100667796-100667846	PrEC	prostate:	n/a
24	chr8:100667796-100667846	IMR90	lung:	fetal
25	chr8:100667796-100667846	AoSMC	blood vessel:	n/a
26	chr8:100559503-100559553	SAEC	small airway:	n/a
27	chr8:100464878-100464928	NHBE	bronchial:	n/a
28	chr8:100559503-100559553	BE2_C	brain:	n/a
29	chr8:100716071-100716121	AG04450	lung:	fetal
30	chr8:100708945-100708995	NB4	blood:	n/a
31	chr8:100549849-100549899	AoSMC	blood vessel:	n/a
32	chr8:100464878-100464928	ProgFib	skin:	n/a
33	chr8:100708545-100708595	BE2_C	brain:	n/a
34	chr8:100635039-100635089	HCT-116	colon:	n/a
35	chr8:100635039-100635089	HCM	heart:	n/a
36	chr8:100297748-100297798	HepG2	liver:	n/a
37	chr8:100708945-100708995	NH-A	brain:	n/a
38	chr8:100464878-100464928	AG10803	skin:	n/a
39	chr8:100297748-100297798	HCT-116	colon:	n/a
40	chr8:100649114-100649164	HEK293	kidney:	embryo
41	chr8:100708621-100708671	HIPEpiC	eye:	n/a
42	chr8:100708545-100708595	HIPEpiC	eye:	n/a
43	chr8:100649114-100649164	K562	blood:	n/a
44	chr8:100708945-100708995	GM06990	blood:	n/a
45	chr8:100708621-100708671	A549	lung:	n/a
46	chr8:100708945-100708995	PrEC	prostate:	n/a
47	chr8:100334620-100334670	HCF	heart:	n/a
48	chr8:100297748-100297798	HUVEC	blood vessel:	n/a
49	chr8:100549776-100549826	HCT-116	colon:	n/a
50	chr8:100549849-100549899	HNPCEpiC	eye:	n/a

(count:195 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr8:100525847..100527559-chr8:100529820..100532768,2	MCF-7	breast:
2	chr8:100506206..100508940-chr8:100515378..100517666,2	MCF-7	breast:
3	chr8:100464584..100466784-chr8:100489016..100491472,2	MCF-7	breast:
4	chr8:100615293..100618024-chr8:100620811..100623753,2	MCF-7	breast:
5	chr8:100508680..100510316-chr8:100523382..100526217,2	MCF-7	breast:
6	chr8:100711733..100714570-chr8:100716914..100719775,2	MCF-7	breast:
7	chr11:74032580..74033199-chr8:100370794..100371470,2	MCF-7	breast:
8	chr8:100492530..100494149-chr8:100495886..100498811,2	MCF-7	breast:
9	chr8:100494882..100496542-chr8:100496740..100499297,2	MCF-7	breast:
10	chr8:100700326..100701994-chr8:100715274..100717581,2	K562	blood:
11	chr8:100637655..100639702-chr8:100646117..100648663,2	MCF-7	breast:
12	chr8:100340207..100341801-chr8:100343989..100346691,2	MCF-7	breast:
13	chr8:99180814..99181617-chr8:100370430..100371368,2	MCF-7	breast:
14	chr8:100651536..100655023-chr8:100656332..100658879,3	K562	blood:
15	chr8:99956540..99958741-chr8:100370642..100372359,2	MCF-7	breast:
16	chr8:100450418..100452655-chr8:100468623..100470594,2	K562	blood:
17	chr8:100180104..100181200-chr8:100370523..100371154,5	MCF-7	breast:
18	chr8:100329098..100330856-chr8:100331177..100332983,2	MCF-7	breast:
19	chr8:100380996..100382939-chr8:100386454..100387970,2	K562	blood:
20	chr8:100714775..100716428-chr8:100716613..100718329,2	MCF-7	breast:
21	chr8:100544046..100548556-chr8:100548656..100552103,4	K562	blood:
22	chr8:100354480..100357120-chr8:100365143..100367945,2	K562	blood:
23	chr8:100433911..100436132-chr8:100443954..100446728,2	MCF-7	breast:
24	chr8:100719725..100721462-chr8:100723554..100725582,2	K562	blood:
25	chr8:100415595..100418351-chr8:100620634..100623512,2	MCF-7	breast:
26	chr8:100368561..100370943-chr8:100372272..100375246,2	K562	blood:
27	chr8:100707994..100711279-chr8:100711487..100714977,4	K562	blood:
28	chr8:100559744..100561257-chr8:101041447..101043428,2	K562	blood:
29	chr8:100666079..100668727-chr8:100674262..100677111,3	K562	blood:
30	chr8:100566647..100568766-chr8:100572666..100574996,2	MCF-7	breast:
31	chr8:100662125..100664863-chr8:100667158..100669715,2	MCF-7	breast:
32	chr8:100715387..100717513-chr8:100719961..100722930,2	K562	blood:
33	chr8:100560158..100563558-chr8:100564572..100567827,4	K562	blood:
34	chr8:100732675..100734223-chr8:100737427..100738953,2	K562	blood:
35	chr8:100712738..100714435-chr8:100716061..100717614,2	K562	blood:
36	chr8:100478649..100480256-chr8:100490609..100493235,2	K562	blood:
37	chr8:100731080..100732715-chr8:100738553..100741102,2	MCF-7	breast:
38	chr8:100651536..100655023-chr8:100656332..100658879,3	K562	blood:
39	chr8:100558748..100564214-chr8:100565274..100568136,5	MCF-7	breast:
40	chr8:100641638..100644745-chr8:100644767..100647893,3	K562	blood:
41	chr8:100494882..100496542-chr8:100496740..100499297,2	MCF-7	breast:
42	chr8:100558486..100560693-chr8:100576849..100579778,3	MCF-7	breast:
43	chr8:100731080..100732715-chr8:100738553..100741102,2	MCF-7	breast:
44	chr8:100724026..100725621-chr8:100784325..100786772,2	K562	blood:
45	chr8:100369443..100371664-chr8:100373746..100375749,2	K562	blood:
46	chr8:100444521..100447261-chr8:100451811..100454572,2	K562	blood:
47	chr8:100634441..100637349-chr8:100638779..100641653,3	K562	blood:
48	chr8:100474939..100477291-chr8:100497932..100499895,2	MCF-7	breast:
49	chr8:100505320..100508002-chr8:100513544..100516254,2	K562	blood:
50	chr8:100403279..100404684-chr8:100871403..100872860,7	MCF-7	breast:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-COX6C-2	chr8:100626014-100626306	NONHSAT127958
2	lnc-OSR2-7	chr8:100443749-100443892	NONHSAT127953
3	lnc-OSR2-7	chr8:100401844-100401948	NONHSAT127953
4	lnc-OSR2-7	chr8:100403785-100403932	NONHSAT127953
5	lnc-OSR2-7	chr8:100441798-100441875	NONHSAT127953
6	lnc-OSR2-7	chr8:100454629-100454639	NONHSAT127953
7	lnc-STK3-6	chr8:100352533-100353989	NONHSAT127951
8	lnc-STK3-7	chr8:100358280-100360484	NONHSAT127952

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

No data

Variant related genes	Relation type
RN7SL350P	TF binding region
VPS13B	TF binding region
ENSG00000206699	TF binding region
ENSG00000237704	TF binding region
MIR599	TF binding region
ENSG00000225017	TF binding region
MIR875	TF binding region
ENSG00000235683	TF binding region
RN7SL350P	CpG island
VPS13B	CpG island
ENSG00000206699	CpG island
ENSG00000237704	CpG island
MIR599	CpG island
ENSG00000225017	CpG island
MIR875	CpG island
ENSG00000235683	CpG island
ENSG00000253912	chromatin interactions
ENSG00000164920	chromatin interactions
ENSG00000225017	chromatin interactions
ENSG00000243254	chromatin interactions
ENSG00000169045	chromatin interactions
ENSG00000188029	chromatin interactions
ENSG00000206699	chromatin interactions
ENSG00000207804	chromatin interactions
ENSG00000009307	chromatin interactions
ENSG00000004779	chromatin interactions
ENSG00000132549	chromatin interactions
ENSG00000253948	chromatin interactions
ENSG00000216069	chromatin interactions
ENSG00000235683	chromatin interactions

Extended variants
information (count: 15036 )
Associated
traits (count: 110 )

Variant overlapped rSNPs/rCNVs (count:15036 , 50 per page) page: 1 2 3 4 5 6 7 ... 301

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10089778	chr8:100295634-100295635	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs555874140	chr8:100295644-100295645	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs576330915	chr8:100295699-100295700	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs561124952	chr8:100295704-100295705	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs541651115	chr8:100295705-100295706	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs530204907	chr8:100295734-100295735	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs544952201	chr8:100295744-100295745	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs550220926	chr8:100295758-100295759	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs369760601	chr8:100295785-100295786	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs374199820	chr8:100295828-100295829	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs563965308	chr8:100295838-100295839	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs368259359	chr8:100295840-100295841	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs532404693	chr8:100295927-100295928	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs111669639	chr8:100295987-100295988	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs552539527	chr8:100295995-100295996	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs190657718	chr8:100296096-100296097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs376662537	chr8:100296130-100296131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs7823291	chr8:100296142-100296143	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs139875535	chr8:100296185-100296186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs143307333	chr8:100296190-100296191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs374058923	chr8:100296250-100296251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs182947757	chr8:100296360-100296361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs75500975	chr8:100296418-100296419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs369279519	chr8:100296419-100296420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs146206464	chr8:100296596-100296597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs564392973	chr8:100296597-100296598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs539104603	chr8:100296598-100296599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs552918230	chr8:100296607-100296608	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs571227428	chr8:100296693-100296694	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs572632246	chr8:100296735-100296736	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs186829414	chr8:100296762-100296763	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs148415519	chr8:100296815-100296816	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs142506304	chr8:100296842-100296843	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs151012230	chr8:100296926-100296927	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs112069581	chr8:100296962-100296963	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs67888017	chr8:100296963-100296964	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs563873052	chr8:100296964-100296965	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs56937393	chr8:100296965-100296966	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs34359697	chr8:100296989-100296990	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs377174642	chr8:100297040-100297041	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs532500809	chr8:100297058-100297059	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs552320488	chr8:100297068-100297069	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs559758223	chr8:100297105-100297106	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs528464893	chr8:100297111-100297112	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs139596763	chr8:100297187-100297188	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs568521781	chr8:100297229-100297230	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs144435194	chr8:100297248-100297249	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs536897495	chr8:100297266-100297267	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs550745334	chr8:100297374-100297375	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs541198764	chr8:100297414-100297415	Weak transcription Enhancers	n/a	n/a	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:4242 , 50 per page) page: 1 2 3 4 5 6 7 ... 85

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:100278800-100302400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
2	chr8:100280800-100299000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr8:100284200-100301200	Weak transcription	GM12878-XiMat	blood
4	chr8:100284600-100298200	Weak transcription	Fetal Stomach	stomach
5	chr8:100284600-100312000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr8:100284800-100298800	Weak transcription	Fetal Lung	lung
7	chr8:100284800-100307200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
8	chr8:100285000-100298200	Weak transcription	Adipose Nuclei	Adipose
9	chr8:100285800-100298200	Weak transcription	Lung	lung
10	chr8:100286200-100298000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr8:100286600-100298000	Weak transcription	Rectal Smooth Muscle	rectum
12	chr8:100286600-100298200	Weak transcription	Liver	Liver
13	chr8:100286600-100303000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
14	chr8:100286600-100306000	Weak transcription	Rectal Mucosa Donor 31	rectum
15	chr8:100286800-100298000	Weak transcription	Colon Smooth Muscle	Colon
16	chr8:100286800-100314000	Weak transcription	HSMM	muscle
17	chr8:100287200-100298000	Weak transcription	K562	blood
18	chr8:100288400-100304400	Weak transcription	Primary hematopoietic stem cells	blood
19	chr8:100288800-100298200	Weak transcription	Duodenum Smooth Muscle	Duodenum
20	chr8:100288800-100301600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
21	chr8:100288800-100302200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr8:100288800-100309000	Weak transcription	Primary monocytes fromperipheralblood	blood
23	chr8:100289000-100301600	Weak transcription	Primary B cells from peripheral blood	blood
24	chr8:100290200-100298200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr8:100290400-100298400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
26	chr8:100291000-100301800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
27	chr8:100291000-100303400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
28	chr8:100291200-100301800	Weak transcription	Primary T cells from cord blood	blood
29	chr8:100291200-100301800	Weak transcription	Primary T helper cells PMA-I stimulated	--
30	chr8:100291200-100302200	Weak transcription	Cortex derived primary cultured neurospheres	brain
31	chr8:100291200-100305000	Weak transcription	Dnd41	blood
32	chr8:100291400-100301800	Weak transcription	Psoas Muscle	Psoas
33	chr8:100291600-100298200	Weak transcription	Sigmoid Colon	Sigmoid Colon
34	chr8:100291800-100296800	Weak transcription	Pancreas	Pancrea
35	chr8:100291800-100314400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
36	chr8:100292000-100298400	Weak transcription	Esophagus	oesophagus
37	chr8:100292000-100299200	Weak transcription	HepG2	liver
38	chr8:100292000-100315800	Weak transcription	Ovary	ovary
39	chr8:100292800-100305000	Weak transcription	Fetal Intestine Large	intestine
40	chr8:100293000-100302000	Weak transcription	Monocytes-CD14+_RO01746	blood
41	chr8:100293400-100297600	Weak transcription	HUES64 Cell Line	embryonic stem cell
42	chr8:100293600-100297800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr8:100293600-100298000	Weak transcription	HUES6 Cell Line	embryonic stem cell
44	chr8:100293600-100298800	Weak transcription	Fetal Intestine Small	intestine
45	chr8:100293600-100301800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr8:100293600-100303000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr8:100293600-100304400	Weak transcription	Right Ventricle	heart
48	chr8:100293800-100296800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr8:100293800-100298800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr8:100293800-100305200	Weak transcription	Breast Myoepithelial Primary Cells	Breast

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links