Variant report

Variant	nsv831245
Chromosome Location	chr8:17113083-17308408
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1760)
CpG islands
(count:1893)
Chromatin interactive
region (count:110)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1760 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:17142585-17142622	K562	blood:	n/a	n/a
2	ARID3A	chr8:17178387-17178503	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:17178754-17179567	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:17220430-17220635	K562	blood:	n/a	n/a
5	ARID3A	chr8:17186370-17187080	HepG2	liver:	n/a	n/a
6	ARID3A	chr8:17113181-17113722	K562	blood:	n/a	n/a
7	ARID3A	chr8:17191497-17192169	HepG2	liver:	n/a	chr8:17191772-17191788
8	ARID3A	chr8:17250688-17251360	HepG2	liver:	n/a	n/a
9	ARID3A	chr8:17208679-17208925	HepG2	liver:	n/a	n/a
10	ARID3A	chr8:17116880-17117553	HepG2	liver:	n/a	n/a
11	ATF1	chr8:17220231-17220797	K562	blood:	n/a	n/a
12	ATF2	chr8:17231427-17231818	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF3	chr8:17220560-17220891	K562	blood:	n/a	n/a
14	ATF3	chr8:17220232-17220479	K562	blood:	n/a	n/a
15	BACH1	chr8:17113555-17113700	K562	blood:	n/a	n/a
16	BACH1	chr8:17301773-17301896	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr8:17252892-17252994	K562	blood:	n/a	n/a
18	BACH1	chr8:17270645-17271426	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr8:17231457-17231724	H1-hESC	embryonic stem cell:	n/a	chr8:17231613-17231627
20	BCL3	chr8:17178772-17179387	A549	lung:	n/a	n/a
21	BCL3	chr8:17166314-17166673	A549	lung:	n/a	n/a
22	BHLHE40	chr8:17220324-17220853	K562	blood:	n/a	n/a
23	BHLHE40	chr8:17194049-17194399	HepG2	liver:	n/a	n/a
24	BHLHE40	chr8:17178997-17179343	HepG2	liver:	n/a	n/a
25	BHLHE40	chr8:17123935-17124272	K562	blood:	n/a	n/a
26	BHLHE40	chr8:17195466-17195864	HepG2	liver:	n/a	chr8:17195640-17195653 chr8:17195641-17195650 chr8:17195636-17195657
27	BRCA1	chr8:17191553-17191839	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr8:17194222-17194259	HepG2	liver:	n/a	n/a
29	BRCA1	chr8:17297707-17297907	GM12878	blood:	n/a	n/a
30	BRCA1	chr8:17191526-17191803	H1-hESC	embryonic stem cell:	n/a	n/a
31	BRCA1	chr8:17258135-17258425	Hela-S3	cervix:	n/a	n/a
32	BRCA1	chr8:17219754-17220279	Hela-S3	cervix:	n/a	n/a
33	CBX3	chr8:17118144-17118474	K562	blood:	n/a	n/a
34	CBX3	chr8:17123929-17124228	K562	blood:	n/a	n/a
35	CBX3	chr8:17166997-17167286	K562	blood:	n/a	n/a
36	CCNT2	chr8:17220565-17220774	K562	blood:	n/a	n/a
37	CCNT2	chr8:17123986-17124198	K562	blood:	n/a	chr8:17124108-17124128
38	CEBPB	chr8:17193914-17194335	HepG2	liver:	n/a	n/a
39	CEBPB	chr8:17113300-17113689	K562	blood:	n/a	n/a
40	CEBPB	chr8:17186321-17187025	HepG2	liver:	n/a	chr8:17186750-17186761
41	CEBPB	chr8:17296497-17296716	A549	lung:	n/a	n/a
42	CEBPB	chr8:17210331-17210654	IMR90	lung:	n/a	n/a
43	CEBPB	chr8:17198666-17198949	MCF-7	breast:	n/a	n/a
44	CEBPB	chr8:17191494-17192095	Hela-S3	cervix:	n/a	chr8:17191532-17191545
45	CEBPB	chr8:17142470-17142562	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr8:17296520-17296709	K562	blood:	n/a	n/a
47	CEBPB	chr8:17186426-17186897	K562	blood:	n/a	chr8:17186750-17186761
48	CEBPB	chr8:17179013-17179333	MCF-7	breast:	n/a	chr8:17179179-17179190
49	CEBPB	chr8:17276882-17277572	HepG2	liver:	n/a	chr8:17277396-17277407
50	CEBPB	chr8:17122866-17123219	IMR90	lung:	n/a	chr8:17123038-17123051 chr8:17123038-17123049

(count:1893 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:17271322-17271372	A549	lung:	n/a
2	chr8:17271322-17271372	HAEpiC	amniotic membrane:	n/a
3	chr8:17271322-17271372	A549	lung:	n/a
4	chr8:17271322-17271372	HAEpiC	amniotic membrane:	n/a
5	chr8:17212177-17212227	HEEpiC	esophagus:	n/a
6	chr8:17269638-17269688	SK-N-MC	brain:	n/a
7	chr8:17271067-17271117	PFSK-1	brain:	n/a
8	chr8:17172345-17172395	NH-A	brain:	n/a
9	chr8:17271067-17271117	HAEpiC	amniotic membrane:	n/a
10	chr8:17270608-17270658	MCF10A-Er-Src	breast:	n/a
11	chr8:17272669-17272719	HEK293	kidney:	embryo
12	chr8:17272669-17272719	PrEC	prostate:	n/a
13	chr8:17270834-17270884	BE2_C	brain:	n/a
14	chr8:17271322-17271372	BJ	skin:	n/a
15	chr8:17271105-17271155	HRCEpiC	kidney:	n/a
16	chr8:17249585-17249635	U87	brain:	n/a
17	chr8:17206819-17206869	HAEpiC	amniotic membrane:	n/a
18	chr8:17270812-17270862	AG04449	skin:	fetal
19	chr8:17156032-17156082	NT2-D1	testis:	n/a
20	chr8:17272669-17272719	NB4	blood:	n/a
21	chr8:17270834-17270884	HRCEpiC	kidney:	n/a
22	chr8:17269638-17269688	K562	blood:	n/a
23	chr8:17206671-17206721	SAEC	small airway:	n/a
24	chr8:17207503-17207553	NHBE	bronchial:	n/a
25	chr8:17146201-17146251	HEEpiC	esophagus:	n/a
26	chr8:17271322-17271372	HNPCEpiC	eye:	n/a
27	chr8:17132476-17132526	HAEpiC	amniotic membrane:	n/a
28	chr8:17270452-17270502	SAEC	small airway:	n/a
29	chr8:17195444-17195494	MCF10A-Er-Src	breast:	n/a
30	chr8:17206819-17206869	ECC-1	luminal epithelium:	n/a
31	chr8:17249585-17249635	ECC-1	luminal epithelium:	n/a
32	chr8:17225669-17225719	Jurkat	blood:	n/a
33	chr8:17270608-17270658	ovcar-3	ovarian:	n/a
34	chr8:17146201-17146251	K562	blood:	n/a
35	chr8:17206671-17206721	NB4	blood:	n/a
36	chr8:17271067-17271117	K562	blood:	n/a
37	chr8:17156032-17156082	PANC-1	pancreas:	n/a
38	chr8:17271093-17271143	NB4	blood:	n/a
39	chr8:17220621-17220671	Hepatocyte	liver:	n/a
40	chr8:17272669-17272719	K562	blood:	n/a
41	chr8:17271535-17271585	Hepatocyte	liver:	n/a
42	chr8:17271535-17271585	SK-N-SH	brain:	n/a
43	chr8:17271340-17271390	ProgFib	skin:	n/a
44	chr8:17220621-17220671	HCF	heart:	n/a
45	chr8:17271067-17271117	CMK	blood:	n/a
46	chr8:17271119-17271169	GM19239	blood:	n/a
47	chr8:17271340-17271390	HUVEC	blood vessel:	n/a
48	chr8:17220621-17220671	GM19239	blood:	n/a
49	chr8:17272520-17272570	HEEpiC	esophagus:	n/a
50	chr8:17272669-17272719	NHBE	bronchial:	n/a

(count:110 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr8:17179041..17179750-chr8:17187082..17187710,2	MCF-7	breast:
2	chr8:17191177..17192005-chr8:17356532..17357392,2	MCF-7	breast:
3	chr8:17276847..17279653-chr8:17286302..17287964,2	MCF-7	breast:
4	chr8:17104368..17106573-chr8:17120538..17122690,2	MCF-7	breast:
5	chr8:17101844..17108322-chr8:17108585..17113384,10	MCF-7	breast:
6	chr8:17014641..17017128-chr8:17111779..17114711,2	MCF-7	breast:
7	chr8:17187262..17190633-chr8:17192201..17193800,3	K562	blood:
8	chr8:17138059..17140841-chr8:17141112..17143535,3	K562	blood:
9	chr8:17104295..17106000-chr8:17189197..17192059,2	MCF-7	breast:
10	chr8:17129178..17133989-chr8:17134678..17139635,6	K562	blood:
11	chr8:17186901..17187810-chr8:17385032..17385929,4	MCF-7	breast:
12	chr8:17289595..17291607-chr8:17293310..17295677,2	K562	blood:
13	chr8:17150961..17152900-chr8:17155018..17157841,2	K562	blood:
14	chr8:17115664..17117954-chr8:17120859..17122957,2	K562	blood:
15	chr8:17187221..17187826-chr8:17352337..17353156,2	MCF-7	breast:
16	chr8:17186034..17190747-chr8:17394369..17399926,6	MCF-7	breast:
17	chr8:17250670..17253402-chr8:17269426..17272264,2	MCF-7	breast:
18	chr8:17136101..17138499-chr8:17144330..17145871,2	K562	blood:
19	chr8:17115664..17117954-chr8:17120859..17122957,2	K562	blood:
20	chr8:17135271..17136170-chr8:17186836..17187820,2	MCF-7	breast:
21	chr8:17170658..17172303-chr8:17176472..17178856,2	K562	blood:
22	chr8:17185558..17187741-chr8:17196710..17199457,2	MCF-7	breast:
23	chr8:17186885..17187690-chr8:17397408..17398233,2	MCF-7	breast:
24	chr8:17186941..17187626-chr8:17346814..17347814,3	MCF-7	breast:
25	chr8:17235148..17236985-chr8:17238240..17239908,2	K562	blood:
26	chr8:17173102..17174609-chr8:17174668..17176394,2	MCF-7	breast:
27	chr8:17103627..17106948-chr8:17118795..17122287,3	MCF-7	breast:
28	chr8:17190775..17193480-chr8:17271375..17272921,2	MCF-7	breast:
29	chr8:17190775..17193480-chr8:17271375..17272921,2	MCF-7	breast:
30	chr8:17110387..17113117-chr8:17114001..17116869,2	MCF-7	breast:
31	chr8:17185049..17194238-chr8:17354082..17360158,11	MCF-7	breast:
32	chr8:17170658..17172303-chr8:17176472..17178856,2	K562	blood:
33	chr8:17172664..17174394-chr8:17176927..17179156,2	MCF-7	breast:
34	chr8:17186302..17188819-chr8:17435288..17438238,2	MCF-7	breast:
35	chr8:17110387..17113117-chr8:17114001..17116869,2	MCF-7	breast:
36	chr8:17136101..17138499-chr8:17144330..17145871,2	K562	blood:
37	chr8:17250437..17252922-chr8:17255760..17257352,2	K562	blood:
38	chr8:17269598..17272556-chr8:17279087..17281001,2	K562	blood:
39	chr8:17192347..17195027-chr8:17395405..17397389,2	MCF-7	breast:
40	chr8:17190481..17192465-chr8:17193917..17196477,2	MCF-7	breast:
41	chr8:17301065..17302632-chr8:17303948..17305994,2	K562	blood:
42	chr8:17276847..17279653-chr8:17286302..17287964,2	MCF-7	breast:
43	chr8:17079418..17082385-chr8:17123584..17126434,2	K562	blood:
44	chr8:17301065..17302632-chr8:17303948..17305994,2	K562	blood:
45	chr8:17172664..17174394-chr8:17176927..17179156,2	MCF-7	breast:
46	chr8:17205131..17207334-chr8:17268909..17271300,2	MCF-7	breast:
47	chr8:17300327..17302632-chr8:17304494..17307241,2	K562	blood:
48	chr8:17178413..17182880-chr8:17183196..17188974,7	MCF-7	breast:
49	chr8:17140191..17142110-chr8:17143983..17147187,3	K562	blood:
50	chr8:17160128..17162851-chr8:17175354..17177683,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZDHHC2-3	chr8:17125422-17127659	ncRnaDb_ncrna_FR339864_1

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	VPS37A	hsa-miR-148b-3p	chr8:17152675-17152702

Variant related genes	Relation type
VPS37A	TF binding region
MTMR7	TF binding region
VPS37A	CpG island
MTMR7	CpG island
ENSG00000104219	chromatin interactions
ENSG00000155975	chromatin interactions
ENSG00000198791	chromatin interactions
ENSG00000003989	chromatin interactions
ENSG00000003987	chromatin interactions

Extended variants
information (count: 9182 )
Associated
traits (count: 131 )

Variant overlapped rSNPs/rCNVs (count:9182 , 50 per page) page: 1 2 3 4 5 6 7 ... 184

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs149798415	chr8:17113107-17113108	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs187023873	chr8:17113114-17113115	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs576799470	chr8:17113116-17113117	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs540970865	chr8:17113124-17113125	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs114511273	chr8:17113183-17113184	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs145784115	chr8:17113231-17113232	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs371459898	chr8:17113252-17113253	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs80167731	chr8:17113268-17113269	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs111533669	chr8:17113273-17113274	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs537841884	chr8:17113294-17113295	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs531979673	chr8:17113332-17113333	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs189449032	chr8:17113333-17113334	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs11779174	chr8:17113349-17113350	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs181519250	chr8:17113355-17113356	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs548620705	chr8:17113357-17113358	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs140963450	chr8:17113359-17113360	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs574571090	chr8:17113395-17113396	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs143375572	chr8:17113487-17113488	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs557405210	chr8:17113500-17113501	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs571003976	chr8:17113508-17113509	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs55805233	chr8:17113522-17113523	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs553356943	chr8:17113532-17113533	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs118073623	chr8:17113577-17113578	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs142437203	chr8:17113586-17113587	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs541285556	chr8:17113602-17113603	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs10097407	chr8:17113628-17113629	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs574555252	chr8:17113659-17113660	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs536805314	chr8:17113707-17113708	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs185263809	chr8:17113723-17113724	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs190019159	chr8:17113750-17113751	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs576487651	chr8:17113751-17113752	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs112485902	chr8:17113769-17113770	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs545494569	chr8:17113785-17113786	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs76706244	chr8:17113799-17113800	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs529736602	chr8:17113800-17113801	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs146746839	chr8:17113842-17113843	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs558893244	chr8:17113848-17113849	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs73551456	chr8:17113853-17113854	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs140419238	chr8:17113896-17113897	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs548848530	chr8:17113905-17113906	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs183361525	chr8:17113906-17113907	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs531130662	chr8:17113933-17113934	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs550932548	chr8:17113935-17113936	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs371855120	chr8:17113994-17113995	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs571060882	chr8:17114043-17114044	Weak transcription Enhancers Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs140479043	chr8:17114053-17114054	Weak transcription Enhancers Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs539913505	chr8:17114063-17114064	Weak transcription Enhancers Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs10111267	chr8:17114128-17114129	Weak transcription Enhancers Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs141925092	chr8:17114140-17114141	Weak transcription Enhancers Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs566856769	chr8:17114174-17114175	Weak transcription Enhancers Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:131)

Disease	PMID	Source
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	17603634	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	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
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Colorectal cancer	17229543	CNVD
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
small cell lung cancer	20016488	CNVD
Autism	22495311	CNVD
Colorectal cancer	16774939	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Epilepsy	22083797	CNVD
Cancer	18840272	CNVD
Epithelial cancer	20478067	CNVD
Non-small cell lung cancer	19010865	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Intracranial arachnoid cysts	17641416	CNVD
Breast cancer	19287154	CNVD
Breast cancer	21956041	CNVD
Gastric adenocarcinoma	19115996	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Colorectal cancer	19455253	CNVD
Prostate cancer	17217626	CNVD
Cervical cancer	16585170	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	21177765	CNVD
Bladder cancer	21909424	CNVD
Multiple myeloma	17550852	CNVD
Pancreatic cancer	21811587	CNVD
Schizophrenia	19197363	CNVD
Breast cancer	21364760	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Prostate cancer	22341455	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Osteosarcoma	21215367	CNVD
Renal cell carcinoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:2756 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:17105400-17113200	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr8:17106000-17113800	Weak transcription	Lung	lung
3	chr8:17106000-17118400	Weak transcription	Small Intestine	intestine
4	chr8:17106000-17119200	Weak transcription	Left Ventricle	heart
5	chr8:17106000-17124000	Weak transcription	Placenta	Placenta
6	chr8:17106000-17127400	Weak transcription	Gastric	stomach
7	chr8:17106000-17127800	Weak transcription	Brain Substantia Nigra	brain
8	chr8:17106000-17135400	Weak transcription	Fetal Heart	heart
9	chr8:17106200-17118000	Weak transcription	Primary T cells fromperipheralblood	blood
10	chr8:17106200-17119200	Weak transcription	HSMM	muscle
11	chr8:17106200-17125200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr8:17106200-17126400	Weak transcription	Fetal Thymus	thymus
13	chr8:17106200-17127400	Weak transcription	Fetal Stomach	stomach
14	chr8:17106400-17113200	Weak transcription	Primary monocytes fromperipheralblood	blood
15	chr8:17106400-17113200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
16	chr8:17106400-17127400	Weak transcription	HSMMtube	muscle
17	chr8:17106600-17113200	Enhancers	Liver	Liver
18	chr8:17106600-17113200	Weak transcription	Rectal Smooth Muscle	rectum
19	chr8:17106600-17113200	Weak transcription	NH-A	brain
20	chr8:17106600-17115200	Weak transcription	Cortex derived primary cultured neurospheres	brain
21	chr8:17106600-17115800	Weak transcription	Fetal Lung	lung
22	chr8:17106600-17125400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr8:17106600-17127200	Weak transcription	Rectal Mucosa Donor 29	rectum
24	chr8:17106600-17127400	Weak transcription	Fetal Intestine Large	intestine
25	chr8:17106800-17113200	Weak transcription	Skeletal Muscle Male	skeletal muscle
26	chr8:17106800-17115600	Weak transcription	Primary neutrophils fromperipheralblood	blood
27	chr8:17106800-17116800	Weak transcription	Primary B cells from cord blood	blood
28	chr8:17106800-17119000	Weak transcription	Fetal Intestine Small	intestine
29	chr8:17106800-17126600	Weak transcription	Fetal Kidney	kidney
30	chr8:17107000-17113200	Weak transcription	NHLF	lung
31	chr8:17107200-17113200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr8:17107400-17113200	Weak transcription	Monocytes-CD14+_RO01746	blood
33	chr8:17107400-17115400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr8:17107400-17127800	Weak transcription	Brain Inferior Temporal Lobe	brain
35	chr8:17107600-17113200	Weak transcription	NHDF-Ad	bronchial
36	chr8:17107600-17115800	Weak transcription	Brain Angular Gyrus	brain
37	chr8:17107600-17116600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr8:17107600-17126600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr8:17107800-17127400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr8:17108800-17113200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr8:17108800-17127400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr8:17109600-17126800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
43	chr8:17110000-17114600	Enhancers	Duodenum Mucosa	Duodenum
44	chr8:17110000-17127200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
45	chr8:17110600-17113200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr8:17110800-17122400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr8:17111200-17114000	Enhancers	Primary hematopoietic stem cells short term culture	blood
48	chr8:17111400-17114600	Enhancers	Muscle Satellite Cultured Cells	--
49	chr8:17111600-17114000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr8:17111600-17114400	Enhancers	Stomach Mucosa	stomach

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