Variant report

Variant	esv1844500
Chromosome Location	chr8:17079438-17161374
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1546)
CpG islands
(count:1221)
Chromatin interactive
region (count:78)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:1546 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:17105049-17105298	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:17113181-17113722	K562	blood:	n/a	n/a
3	ARID3A	chr8:17104253-17104606	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:17083853-17084051	HepG2	liver:	n/a	n/a
5	ARID3A	chr8:17111557-17112129	K562	blood:	n/a	n/a
6	ARID3A	chr8:17116880-17117553	HepG2	liver:	n/a	n/a
7	ARID3A	chr8:17107360-17107370	K562	blood:	n/a	n/a
8	ARID3A	chr8:17142585-17142622	K562	blood:	n/a	n/a
9	ARID3A	chr8:17104336-17104477	K562	blood:	n/a	n/a
10	ATF1	chr8:17103606-17104598	K562	blood:	n/a	n/a
11	ATF1	chr8:17111646-17111934	K562	blood:	n/a	n/a
12	ATF2	chr8:17103724-17104706	GM12878	blood:	n/a	n/a
13	ATF2	chr8:17103681-17104094	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF3	chr8:17103824-17104563	K562	blood:	n/a	chr8:17103979-17103992 chr8:17104116-17104125 chr8:17104378-17104398 chr8:17104139-17104147 chr8:17104425-17104434 chr8:17104041-17104049 chr8:17103980-17104000
15	ATF3	chr8:17104149-17104545	K562	blood:	n/a	chr8:17104378-17104398 chr8:17104425-17104434
16	ATF3	chr8:17103845-17104126	K562	blood:	n/a	chr8:17103979-17103992 chr8:17104116-17104125 chr8:17104041-17104049 chr8:17103980-17104000
17	ATF3	chr8:17104144-17104546	H1-hESC	embryonic stem cell:	n/a	chr8:17104378-17104398 chr8:17104425-17104434
18	ATF3	chr8:17104241-17104452	GM12878	blood:	n/a	chr8:17104378-17104398 chr8:17104425-17104434
19	ATF3	chr8:17104168-17104551	HepG2	liver:	n/a	chr8:17104378-17104398 chr8:17104425-17104434
20	ATF3	chr8:17103802-17104122	H1-hESC	embryonic stem cell:	n/a	chr8:17103979-17103992 chr8:17104041-17104049 chr8:17103980-17104000
21	ATF3	chr8:17104131-17104792	GM12878	blood:	n/a	chr8:17104378-17104398 chr8:17104139-17104147 chr8:17104425-17104434
22	ATF3	chr8:17103854-17104567	H1-hESC	embryonic stem cell:	n/a	chr8:17103979-17103992 chr8:17104116-17104125 chr8:17104378-17104398 chr8:17104139-17104147 chr8:17104425-17104434 chr8:17104041-17104049 chr8:17103980-17104000
23	BACH1	chr8:17113555-17113700	K562	blood:	n/a	n/a
24	BACH1	chr8:17105128-17105419	K562	blood:	n/a	n/a
25	BACH1	chr8:17105125-17105374	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr8:17104391-17104702	H1-hESC	embryonic stem cell:	n/a	n/a
27	BCL3	chr8:17104171-17104733	A549	lung:	n/a	n/a
28	BCLAF1	chr8:17104087-17104663	GM12878	blood:	n/a	n/a
29	BHLHE40	chr8:17103837-17104565	GM12878	blood:	n/a	n/a
30	BHLHE40	chr8:17103735-17104602	HepG2	liver:	n/a	n/a
31	BHLHE40	chr8:17103586-17104670	K562	blood:	n/a	n/a
32	BHLHE40	chr8:17123935-17124272	K562	blood:	n/a	n/a
33	BHLHE40	chr8:17112761-17112988	K562	blood:	n/a	n/a
34	BRCA1	chr8:17104212-17104579	GM12878	blood:	n/a	n/a
35	BRCA1	chr8:17103815-17103992	H1-hESC	embryonic stem cell:	n/a	n/a
36	BRCA1	chr8:17103667-17104607	Hela-S3	cervix:	n/a	n/a
37	BRCA1	chr8:17104305-17104579	HepG2	liver:	n/a	n/a
38	BRCA1	chr8:17104225-17104547	H1-hESC	embryonic stem cell:	n/a	n/a
39	BRCA1	chr8:17103658-17103815	GM12878	blood:	n/a	n/a
40	CBX3	chr8:17123929-17124228	K562	blood:	n/a	n/a
41	CBX3	chr8:17083691-17084289	HCT-116	colon:	n/a	n/a
42	CBX3	chr8:17083672-17084233	HCT-116	colon:	n/a	n/a
43	CBX3	chr8:17103651-17104572	K562	blood:	n/a	n/a
44	CBX3	chr8:17084561-17084945	K562	blood:	n/a	n/a
45	CBX3	chr8:17082722-17083068	HCT-116	colon:	n/a	n/a
46	CBX3	chr8:17118144-17118474	K562	blood:	n/a	n/a
47	CCNT2	chr8:17123986-17124198	K562	blood:	n/a	chr8:17124108-17124128
48	CCNT2	chr8:17103658-17105394	K562	blood:	n/a	chr8:17104425-17104434 chr8:17104145-17104154 chr8:17104116-17104125 chr8:17104016-17104025
49	CEBPB	chr8:17110359-17110722	H1-hESC	embryonic stem cell:	n/a	chr8:17110533-17110544
50	CEBPB	chr8:17112319-17112700	K562	blood:	n/a	n/a

(count:1221 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:17101978-17102028	GM19239	blood:	n/a
2	chr8:17101978-17102028	GM19239	blood:	n/a
3	chr8:17111199-17111249	HAEpiC	amniotic membrane:	n/a
4	chr8:17132476-17132526	SK-N-SH_RA	brain:	n/a
5	chr8:17107551-17107601	ProgFib	skin:	n/a
6	chr8:17089328-17089378	BJ	skin:	n/a
7	chr8:17104852-17104902	NHDF-neo	bronchial:	n/a
8	chr8:17100916-17100966	SKMC	muscle:	n/a
9	chr8:17111199-17111249	CMK	blood:	n/a
10	chr8:17104065-17104115	NT2-D1	testis:	n/a
11	chr8:17102212-17102262	AG09319	gingival:	n/a
12	chr8:17100916-17100966	AG09309	skin:	n/a
13	chr8:17107551-17107601	MCF10A-Er-Src	breast:	n/a
14	chr8:17089328-17089378	H1-hESC	embryonic stem cell:	embryo
15	chr8:17104072-17104122	NHDF-neo	bronchial:	n/a
16	chr8:17104503-17104553	Hepatocyte	liver:	n/a
17	chr8:17102212-17102262	SK-N-SH	brain:	n/a
18	chr8:17100916-17100966	HepG2	liver:	n/a
19	chr8:17104072-17104122	GM06990	blood:	n/a
20	chr8:17100916-17100966	GM06990	blood:	n/a
21	chr8:17146201-17146251	HUVEC	blood vessel:	n/a
22	chr8:17104535-17104585	HMEC	breast:	n/a
23	chr8:17132476-17132526	GM12892	blood:	n/a
24	chr8:17104473-17104523	AoSMC	blood vessel:	n/a
25	chr8:17107551-17107601	HCF	heart:	n/a
26	chr8:17104503-17104553	RPTEC	kidney:	n/a
27	chr8:17132476-17132526	LNCaP	prostate:	n/a
28	chr8:17104473-17104523	HMEC	breast:	n/a
29	chr8:17103891-17103941	NB4	blood:	n/a
30	chr8:17104473-17104523	HepG2	liver:	n/a
31	chr8:17103891-17103941	GM06990	blood:	n/a
32	chr8:17104072-17104122	NT2-D1	testis:	n/a
33	chr8:17104280-17104330	Caco-2	colon:	n/a
34	chr8:17132476-17132526	HepG2	liver:	n/a
35	chr8:17132476-17132526	PANC-1	pancreas:	n/a
36	chr8:17146201-17146251	HCT-116	colon:	n/a
37	chr8:17156032-17156082	HAEpiC	amniotic membrane:	n/a
38	chr8:17156032-17156082	A549	lung:	n/a
39	chr8:17104065-17104115	CMK	blood:	n/a
40	chr8:17132476-17132526	T-47D	breast:	n/a
41	chr8:17089328-17089378	HEK293	kidney:	embryo
42	chr8:17102212-17102262	HepG2	liver:	n/a
43	chr8:17088077-17088127	LNCaP	prostate:	n/a
44	chr8:17104473-17104523	HRE	kidney:	n/a
45	chr8:17104852-17104902	BE2_C	brain:	n/a
46	chr8:17146201-17146251	AG10803	skin:	n/a
47	chr8:17089328-17089378	AG04450	lung:	fetal
48	chr8:17100916-17100966	HUVEC	blood vessel:	n/a
49	chr8:17103891-17103941	HUVEC	blood vessel:	n/a
50	chr8:17104535-17104585	NB4	blood:	n/a

(count:78 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:17115664..17117954-chr8:17120859..17122957,2	K562	blood:
2	chr8:17074146..17076281-chr8:17078184..17080638,2	K562	blood:
3	chr8:17140191..17142110-chr8:17143983..17147187,3	K562	blood:
4	chr8:17012171..17015039-chr8:17137782..17140431,2	K562	blood:
5	chr8:17135271..17136170-chr8:17186836..17187820,2	MCF-7	breast:
6	chr8:17036829..17039360-chr8:17105377..17107304,2	K562	blood:
7	chr8:17090692..17093437-chr8:17102882..17104436,2	MCF-7	breast:
8	chr8:17110957..17112690-chr8:17114362..17116023,2	K562	blood:
9	chr8:17131674..17134373-chr8:17137994..17139635,2	K562	blood:
10	chr8:17052650..17055641-chr8:17099108..17101284,3	K562	blood:
11	chr8:17103405..17106037-chr8:17123266..17125457,2	K562	blood:
12	chr3:195808775..195809379-chr8:17104143..17104871,2	HCT-116	colon:
13	chr8:17082323..17084960-chr8:17097476..17098979,2	K562	blood:
14	chr8:17129178..17133989-chr8:17134678..17139635,6	K562	blood:
15	chr8:17154029..17156637-chr8:17158716..17161062,2	K562	blood:
16	chr8:17013585..17016545-chr8:17102418..17104386,2	K562	blood:
17	chr8:17110957..17112690-chr8:17114362..17116023,2	K562	blood:
18	chr8:17091056..17094283-chr8:17102795..17106838,3	MCF-7	breast:
19	chr12:57039304..57040016-chr8:17103760..17104498,2	Hela-S3	cervix:
20	chr8:17068465..17071226-chr8:17096236..17098022,2	K562	blood:
21	chr8:17072989..17075646-chr8:17078949..17080638,2	K562	blood:
22	chr8:17161041..17163423-chr8:17166244..17169042,3	K562	blood:
23	chr8:17107517..17109054-chr8:17158716..17161350,2	K562	blood:
24	chr8:17093844..17098012-chr8:17107081..17109773,3	K562	blood:
25	chr8:17103075..17105052-chr8:17136390..17138704,2	K562	blood:
26	chr8:17091056..17094283-chr8:17102795..17106838,3	MCF-7	breast:
27	chr8:17082985..17085632-chr8:17102341..17106032,3	K562	blood:
28	chr8:17079418..17082385-chr8:17123584..17126434,2	K562	blood:
29	chr8:17136101..17138499-chr8:17144330..17145871,2	K562	blood:
30	chr8:17104501..17106281-chr8:17779178..17781886,2	K562	blood:
31	chr8:17090389..17093218-chr8:17095428..17097347,2	MCF-7	breast:
32	chr5:34915050..34916049-chr8:17104208..17105025,2	HCT-116	colon:
33	chr8:17103103..17105617-chr8:17126834..17129473,2	K562	blood:
34	chr8:17135640..17137186-chr8:17138924..17140760,2	K562	blood:
35	chr8:17104218..17105878-chr8:17115351..17117747,2	MCF-7	breast:
36	chr8:17135210..17137746-chr8:17141581..17143958,2	MCF-7	breast:
37	chr8:17138059..17140841-chr8:17141112..17143535,3	K562	blood:
38	chr8:17088614..17091950-chr8:17095988..17099514,3	MCF-7	breast:
39	chr8:17076430..17079150-chr8:17079914..17082613,2	K562	blood:
40	chr8:17138059..17140841-chr8:17141112..17143535,3	K562	blood:
41	chr8:17013321..17015459-chr8:17099599..17101771,2	K562	blood:
42	chr8:17013321..17015650-chr8:17098782..17101099,2	K562	blood:
43	chr8:17135640..17137186-chr8:17138924..17140760,2	K562	blood:
44	chr8:17140191..17142110-chr8:17143983..17147187,3	K562	blood:
45	chr8:17110387..17113117-chr8:17114001..17116869,2	MCF-7	breast:
46	chr8:17079418..17082385-chr8:17123584..17126434,2	K562	blood:
47	chr3:122233292..122233835-chr8:17104400..17105266,2	Hela-S3	cervix:
48	chr8:17136101..17138499-chr8:17144330..17145871,2	K562	blood:
49	chr8:17094767..17096866-chr8:17102353..17106553,3	MCF-7	breast:
50	chr8:17101844..17108322-chr8:17108585..17113384,10	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZDHHC2-3	chr8:17125422-17127659	ncRnaDb_ncrna_FR339864_1
2	lnc-ZDHHC2-2	chr8:17081051-17083288	NONHSAT125265
3	lnc-CNOT7-2	chr8:17082473-17082978	ENSG00000271948.1
4	lnc-MTMR7-2	chr8:17102249-17102756	NONHSAT125269
5	lnc-MTMR7-2	chr8:17104184-17104374	NONHSAT125269

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	CNOT7	hsa-miR-106b-5p	chr8:17087802-17087795
2	CNOT7	hsa-miR-106b-5p	chr8:17087796-17087815
3	VPS37A	hsa-miR-148b-3p	chr8:17152675-17152702

Variant related genes	Relation type
ENSG00000271948	TF binding region
VPS37A	TF binding region
CNOT7	TF binding region
ENSG00000271948	CpG island
VPS37A	CpG island
CNOT7	CpG island
ENSG00000113456	chromatin interactions
ENSG00000114030	chromatin interactions
ENSG00000072274	chromatin interactions
ENSG00000271948	chromatin interactions
ENSG00000078674	chromatin interactions
ENSG00000104219	chromatin interactions
ENSG00000101040	chromatin interactions
ENSG00000003989	chromatin interactions
ENSG00000267882	chromatin interactions
ENSG00000113460	chromatin interactions
ENSG00000198791	chromatin interactions
ENSG00000110955	chromatin interactions
ENSG00000155975	chromatin interactions

Extended variants
information (count: 4026 )
Associated
traits (count: 126 )

Variant overlapped rSNPs/rCNVs (count:4026 , 50 per page) page: 1 2 3 4 5 6 7 ... 81

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13278086	chr8:17079438-17079439	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs536592779	chr8:17079443-17079444	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs367744092	chr8:17079488-17079489	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs200415282	chr8:17079489-17079490	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs554644413	chr8:17079490-17079491	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs60190089	chr8:17079509-17079510	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs397892365	chr8:17079510-17079511	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs569374769	chr8:17079536-17079537	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs576747665	chr8:17079570-17079571	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs545629991	chr8:17079577-17079578	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs55953383	chr8:17079588-17079589	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs567932298	chr8:17079589-17079590	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs74406481	chr8:17079655-17079656	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs185850460	chr8:17079705-17079706	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs11555946	chr8:17079711-17079712	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs541374161	chr8:17079722-17079723	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs561165207	chr8:17079739-17079740	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs143944990	chr8:17079772-17079773	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs548893236	chr8:17079792-17079793	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs188268793	chr8:17079812-17079813	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs147305441	chr8:17079840-17079841	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs139948954	chr8:17079848-17079849	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs571281344	chr8:17079875-17079876	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs533693734	chr8:17079972-17079973	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs149426185	chr8:17079974-17079975	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs375920768	chr8:17079975-17079976	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs536919481	chr8:17080071-17080072	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs57994760	chr8:17080095-17080096	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs538553153	chr8:17080097-17080098	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs536933983	chr8:17080168-17080169	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs11271419	chr8:17080240-17080241	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs61477432	chr8:17080242-17080243	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs201253218	chr8:17080264-17080265	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs556859096	chr8:17080279-17080280	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs180677071	chr8:17080340-17080341	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs570381863	chr8:17080358-17080359	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs185989430	chr8:17080370-17080371	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs558892936	chr8:17080387-17080388	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs369627685	chr8:17080402-17080403	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs541212431	chr8:17080474-17080475	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs192146022	chr8:17080477-17080478	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs556579550	chr8:17080489-17080490	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs537206179	chr8:17080517-17080518	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs574775155	chr8:17080525-17080526	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs540729168	chr8:17080534-17080535	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs548483978	chr8:17080553-17080554	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs566873561	chr8:17080562-17080563	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs543434056	chr8:17080569-17080570	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs534313609	chr8:17080590-17080591	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs144853711	chr8:17080616-17080617	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:126)

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
Prostate cancer	22341455	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:2989 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:17027600-17083800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr8:17028800-17083800	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr8:17034200-17087400	Weak transcription	Left Ventricle	heart
4	chr8:17036800-17084400	Weak transcription	Thymus	Thymus
5	chr8:17039000-17087400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
6	chr8:17041000-17090800	Weak transcription	Pancreas	Pancrea
7	chr8:17041800-17083800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
8	chr8:17042000-17084400	Weak transcription	Duodenum Mucosa	Duodenum
9	chr8:17042200-17083800	Weak transcription	Fetal Muscle Leg	muscle
10	chr8:17042200-17084400	Weak transcription	Colon Smooth Muscle	Colon
11	chr8:17042200-17090400	Weak transcription	Gastric	stomach
12	chr8:17042200-17103600	Weak transcription	Aorta	Aorta
13	chr8:17043200-17084000	Weak transcription	Fetal Muscle Trunk	muscle
14	chr8:17043400-17083200	Weak transcription	Fetal Brain Female	brain
15	chr8:17043400-17083800	Weak transcription	Cortex derived primary cultured neurospheres	brain
16	chr8:17043400-17084600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
17	chr8:17043600-17083800	Weak transcription	Brain Anterior Caudate	brain
18	chr8:17044600-17084600	Weak transcription	Hela-S3	cervix
19	chr8:17044800-17084000	Weak transcription	Brain Germinal Matrix	brain
20	chr8:17044800-17090600	Weak transcription	Fetal Stomach	stomach
21	chr8:17045200-17089200	Weak transcription	Rectal Smooth Muscle	rectum
22	chr8:17045800-17083000	Weak transcription	HSMM	muscle
23	chr8:17045800-17084400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr8:17046200-17084400	Weak transcription	Ovary	ovary
25	chr8:17046400-17082600	Weak transcription	NHLF	lung
26	chr8:17046400-17084200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
27	chr8:17047400-17083800	Weak transcription	Fetal Heart	heart
28	chr8:17047600-17084400	Weak transcription	Sigmoid Colon	Sigmoid Colon
29	chr8:17049200-17084000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
30	chr8:17049800-17084600	Weak transcription	Brain Cingulate Gyrus	brain
31	chr8:17049800-17084600	Weak transcription	Brain Inferior Temporal Lobe	brain
32	chr8:17050600-17084200	Weak transcription	Brain Substantia Nigra	brain
33	chr8:17052800-17089600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr8:17053200-17084200	Weak transcription	Liver	Liver
35	chr8:17053600-17081000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr8:17055800-17081800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr8:17056600-17084000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr8:17057400-17084400	Weak transcription	HSMMtube	muscle
39	chr8:17058000-17090800	Weak transcription	Lung	lung
40	chr8:17058600-17084400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
41	chr8:17059800-17083400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr8:17061800-17090800	Weak transcription	Spleen	Spleen
43	chr8:17062400-17087400	Weak transcription	H9 Cell Line	embryonic stem cell
44	chr8:17062800-17084000	Weak transcription	GM12878-XiMat	blood
45	chr8:17062800-17084600	Weak transcription	Placenta	Placenta
46	chr8:17063000-17084400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
47	chr8:17065200-17103600	Weak transcription	Esophagus	oesophagus
48	chr8:17066000-17084400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
49	chr8:17066400-17079600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr8:17066400-17083800	Weak transcription	A549	lung

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