Variant report

Variant	nsv890364
Chromosome Location	chr8:11654796-11671041
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1213)
CpG islands
(count:1344)
Chromatin interactive
region (count:40)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1213 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:11659794-11660028	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:11660655-11661419	K562	blood:	n/a	n/a
3	ARID3A	chr8:11659764-11660172	K562	blood:	n/a	n/a
4	ARID3A	chr8:11670385-11670535	HepG2	liver:	n/a	n/a
5	ARID3A	chr8:11656441-11656736	HepG2	liver:	n/a	n/a
6	ARID3A	chr8:11656609-11656929	K562	blood:	n/a	n/a
7	ARID3A	chr8:11666175-11666691	HepG2	liver:	n/a	n/a
8	ARID3A	chr8:11657809-11657977	HepG2	liver:	n/a	n/a
9	ARID3A	chr8:11660241-11660402	HepG2	liver:	n/a	n/a
10	ATF1	chr8:11656586-11657065	K562	blood:	n/a	n/a
11	ATF2	chr8:11659666-11660052	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr8:11662812-11663108	K562	blood:	n/a	n/a
13	BACH1	chr8:11660680-11660740	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr8:11666079-11666400	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr8:11659730-11660126	H1-hESC	embryonic stem cell:	n/a	n/a
16	BATF	chr8:11656623-11656908	GM12878	blood:	n/a	n/a
17	BCL3	chr8:11659384-11660037	A549	lung:	n/a	n/a
18	BCLAF1	chr8:11661566-11662077	GM12878	blood:	n/a	n/a
19	BHLHE40	chr8:11659789-11660403	GM12878	blood:	n/a	chr8:11660162-11660178 chr8:11660194-11660210
20	BHLHE40	chr8:11661246-11661368	GM12878	blood:	n/a	n/a
21	BHLHE40	chr8:11662425-11662689	HepG2	liver:	n/a	n/a
22	BHLHE40	chr8:11656691-11657024	K562	blood:	n/a	n/a
23	BHLHE40	chr8:11657867-11657948	GM12878	blood:	n/a	n/a
24	BHLHE40	chr8:11662365-11662751	K562	blood:	n/a	n/a
25	BHLHE40	chr8:11662399-11662624	GM12878	blood:	n/a	n/a
26	BHLHE40	chr8:11654927-11655030	K562	blood:	n/a	n/a
27	BHLHE40	chr8:11663658-11663946	K562	blood:	n/a	n/a
28	BHLHE40	chr8:11659800-11661056	K562	blood:	n/a	chr8:11660162-11660178 chr8:11660194-11660210
29	BRCA1	chr8:11666148-11666197	H1-hESC	embryonic stem cell:	n/a	n/a
30	BRCA1	chr8:11660658-11661794	Hela-S3	cervix:	n/a	n/a
31	BRCA1	chr8:11665673-11665862	HepG2	liver:	n/a	n/a
32	BRCA1	chr8:11659771-11660279	Hela-S3	cervix:	n/a	n/a
33	BRCA1	chr8:11660295-11660433	HepG2	liver:	n/a	n/a
34	CBX3	chr8:11659675-11660453	K562	blood:	n/a	n/a
35	CCNT2	chr8:11659631-11661355	K562	blood:	n/a	n/a
36	CCNT2	chr8:11662396-11662576	K562	blood:	n/a	n/a
37	CCNT2	chr8:11665622-11666304	K562	blood:	n/a	n/a
38	CEBPB	chr8:11668154-11668335	A549	lung:	n/a	chr8:11668261-11668272 chr8:11668260-11668273
39	CEBPB	chr8:11657706-11658067	HepG2	liver:	n/a	n/a
40	CEBPB	chr8:11660678-11661002	K562	blood:	n/a	n/a
41	CEBPB	chr8:11656799-11656989	K562	blood:	n/a	n/a
42	CEBPB	chr8:11670335-11670590	HepG2	liver:	n/a	chr8:11670452-11670463
43	CEBPB	chr8:11666294-11666465	K562	blood:	n/a	n/a
44	CEBPB	chr8:11663260-11663546	HepG2	liver:	n/a	n/a
45	CEBPB	chr8:11657698-11658031	HepG2	liver:	n/a	n/a
46	CEBPB	chr8:11668101-11668454	HepG2	liver:	n/a	chr8:11668261-11668272 chr8:11668260-11668273
47	CEBPB	chr8:11659730-11659942	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr8:11659832-11661066	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr8:11657788-11657954	HepG2	liver:	n/a	n/a
50	CEBPB	chr8:11657652-11657962	HepG2	liver:	n/a	n/a

(count:1344 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:11660061-11660111	BJ	skin:	n/a
2	chr8:11660614-11660664	Hela-S3	cervix:	n/a
3	chr8:11660061-11660111	BJ	skin:	n/a
4	chr8:11660614-11660664	Hela-S3	cervix:	n/a
5	chr8:11663584-11663634	LNCaP	prostate:	n/a
6	chr8:11660109-11660159	PFSK-1	brain:	n/a
7	chr8:11659832-11659882	NB4	blood:	n/a
8	chr8:11656692-11656742	HUVEC	blood vessel:	n/a
9	chr8:11660109-11660159	HCF	heart:	n/a
10	chr8:11666485-11666535	HepG2	liver:	n/a
11	chr8:11659832-11659882	HCT-116	colon:	n/a
12	chr8:11670382-11670432	SKMC	muscle:	n/a
13	chr8:11660030-11660080	GM06990	blood:	n/a
14	chr8:11668491-11668541	NHDF-neo	bronchial:	n/a
15	chr8:11660061-11660111	MCF10A-Er-Src	breast:	n/a
16	chr8:11659970-11660020	SKMC	muscle:	n/a
17	chr8:11663584-11663634	GM12891	blood:	n/a
18	chr8:11659832-11659882	AG04449	skin:	fetal
19	chr8:11660030-11660080	NHBE	bronchial:	n/a
20	chr8:11664728-11664778	HIPEpiC	eye:	n/a
21	chr8:11660209-11660259	SK-N-MC	brain:	n/a
22	chr8:11666017-11666067	PANC-1	pancreas:	n/a
23	chr8:11663584-11663634	GM19239	blood:	n/a
24	chr8:11665843-11665893	K562	blood:	n/a
25	chr8:11660614-11660664	SK-N-MC	brain:	n/a
26	chr8:11660614-11660664	HMEC	breast:	n/a
27	chr8:11664728-11664778	HMEC	breast:	n/a
28	chr8:11659970-11660020	HRE	kidney:	n/a
29	chr8:11659497-11659547	HRE	kidney:	n/a
30	chr8:11660109-11660159	HRE	kidney:	n/a
31	chr8:11666017-11666067	PrEC	prostate:	n/a
32	chr8:11660614-11660664	BE2_C	brain:	n/a
33	chr8:11660061-11660111	HCT-116	colon:	n/a
34	chr8:11659961-11660011	HRPEpiC	eye:	n/a
35	chr8:11660209-11660259	HUVEC	blood vessel:	n/a
36	chr8:11659832-11659882	NHDF-neo	bronchial:	n/a
37	chr8:11666017-11666067	HPAEpiC	pulmonary alveolar:	n/a
38	chr8:11659497-11659547	PANC-1	pancreas:	n/a
39	chr8:11660733-11660783	PFSK-1	brain:	n/a
40	chr8:11660061-11660111	NHDF-neo	bronchial:	n/a
41	chr8:11659832-11659882	BE2_C	brain:	n/a
42	chr8:11660030-11660080	HNPCEpiC	eye:	n/a
43	chr8:11659970-11660020	K562	blood:	n/a
44	chr8:11665969-11666019	SK-N-SH	brain:	n/a
45	chr8:11660061-11660111	GM12891	blood:	n/a
46	chr8:11660614-11660664	ECC-1	luminal epithelium:	n/a
47	chr8:11660109-11660159	HIPEpiC	eye:	n/a
48	chr8:11668491-11668541	MCF-7	breast:	n/a
49	chr8:11670382-11670432	SAEC	small airway:	n/a
50	chr8:11656692-11656742	GM12891	blood:	n/a

(count:40 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:2398309..2399006-chr8:11659548..11660515,2	HCT-116	colon:
2	chr8:11648977..11652066-chr8:11653536..11656484,3	MCF-7	breast:
3	chr8:11660132..11662159-chr8:11687088..11688698,2	MCF-7	breast:
4	chr8:11649932..11653064-chr8:11653128..11655366,3	K562	blood:
5	chr6:24666810..24667602-chr8:11659901..11660485,2	HCT-116	colon:
6	chr8:11663695..11667740-chr8:11686501..11689379,3	MCF-7	breast:
7	chr8:11652587..11657894-chr8:11658127..11661459,7	K562	blood:
8	chr8:11662566..11665636-chr8:11705504..11707081,3	K562	blood:
9	chr8:11663591..11666285-chr8:11668539..11672798,5	K562	blood:
10	chr8:11625747..11629309-chr8:11658765..11661345,4	K562	blood:
11	chr8:11652587..11657894-chr8:11658127..11661459,7	K562	blood:
12	chr8:11658229..11662389-chr8:11662980..11669380,10	MCF-7	breast:
13	chr8:11652965..11656305-chr8:11661939..11664556,3	K562	blood:
14	chr8:11657053..11659855-chr8:11661482..11664070,3	K562	blood:
15	chr8:11653668..11656600-chr8:11658872..11661623,3	MCF-7	breast:
16	chr8:11662802..11665653-chr8:11685244..11688002,2	K562	blood:
17	chr8:11658330..11660255-chr8:11664033..11666074,2	MCF-7	breast:
18	chr8:11658229..11662389-chr8:11662980..11669380,10	MCF-7	breast:
19	chr8:11666673..11669607-chr8:11678720..11681322,2	K562	blood:
20	chr10:52384254..52384940-chr8:11659944..11660800,2	NB4	blood:
21	chr8:11626596..11628658-chr8:11659514..11662088,3	K562	blood:
22	chr8:11658864..11661745-chr8:11724576..11726431,3	MCF-7	breast:
23	chr8:11645433..11648215-chr8:11658187..11661640,5	MCF-7	breast:
24	chr8:11618295..11620623-chr8:11664020..11665628,2	K562	blood:
25	chr17:41465211..41466190-chr8:11659722..11660251,2	Hela-S3	cervix:
26	chr8:11658127..11661675-chr8:11664375..11667732,3	K562	blood:
27	chr8:11650636..11652578-chr8:11653838..11655597,2	K562	blood:
28	chr6:30029044..30029552-chr8:11659926..11660449,2	HCT-116	colon:
29	chr8:11653120..11657894-chr8:11659261..11661744,5	K562	blood:
30	chr8:11659663..11662114-chr8:11670043..11672183,2	K562	blood:
31	chr8:11665243..11667469-chr8:11710761..11712863,3	MCF-7	breast:
32	chr8:11658330..11660255-chr8:11664033..11666074,2	MCF-7	breast:
33	chr8:11647279..11650078-chr8:11653979..11656723,2	MCF-7	breast:
34	chr8:11659426..11661474-chr8:11724613..11726870,3	MCF-7	breast:
35	chr8:11664303..11666890-chr8:11705423..11707941,2	MCF-7	breast:
36	chr8:11624784..11628111-chr8:11660073..11663416,4	MCF-7	breast:
37	chr8:11662199..11664746-chr8:11796348..11798802,2	K562	blood:
38	chr8:11625432..11628777-chr8:11664764..11667821,4	MCF-7	breast:
39	chr8:11658127..11661675-chr8:11664375..11667732,3	K562	blood:
40	chr8:11663266..11668513-chr8:11668832..11673585,5	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NEIL2-2	chr8:11660814-11661009	NONHSAT125087
2	lnc-NEIL2-2	chr8:11660604-11660734	NONHSAT125087
3	lnc-RP11-297N6.4.1-1	chr8:11655437-11655656	NONHSAT125085
4	lnc-RP11-297N6.4.1-1	chr8:11659431-11660021	NONHSAT125085

No data

Variant related genes	Relation type
FDFT1	TF binding region
ENSG00000255046	TF binding region
FDFT1	CpG island
ENSG00000255046	CpG island
ENSG00000154328	chromatin interactions
ENSG00000226200	chromatin interactions
ENSG00000255394	chromatin interactions
ENSG00000255046	chromatin interactions
ENSG00000227203	chromatin interactions
ENSG00000110651	chromatin interactions
ENSG00000164733	chromatin interactions
ENSG00000111802	chromatin interactions
ENSG00000204623	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000079459	chromatin interactions
ENSG00000112304	chromatin interactions
ENSG00000198964	chromatin interactions
ENSG00000066379	chromatin interactions

Extended variants
information (count: 1369 )
Associated
traits (count: 150 )

Variant overlapped rSNPs/rCNVs (count:1369 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2686187	chr8:11654796-11654797	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs557587022	chr8:11654817-11654818	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs138307997	chr8:11654824-11654825	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs546029124	chr8:11654825-11654826	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs368901739	chr8:11654831-11654832	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs79558745	chr8:11654839-11654840	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs73663011	chr8:11654864-11654865	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs548663635	chr8:11654866-11654867	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs146168300	chr8:11654887-11654888	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs529663665	chr8:11654929-11654930	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs371927764	chr8:11654930-11654931	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs139207253	chr8:11654939-11654940	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs563532363	chr8:11654940-11654941	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs543066843	chr8:11654946-11654947	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs2686188	chr8:11654952-11654953	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs369334708	chr8:11654956-11654957	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs550845182	chr8:11654960-11654961	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs375873998	chr8:11654963-11654964	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs570635759	chr8:11654966-11654967	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs371713155	chr8:11654974-11654975	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs368851426	chr8:11654979-11654980	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs142496115	chr8:11654995-11654996	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs547045937	chr8:11655010-11655011	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs568368318	chr8:11655016-11655017	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs73207245	chr8:11655022-11655023	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs556927851	chr8:11655031-11655032	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs376938321	chr8:11655042-11655043	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs539722469	chr8:11655044-11655045	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs201732525	chr8:11655046-11655047	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs143594524	chr8:11655047-11655048	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs59718801	chr8:11655048-11655049	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs377727616	chr8:11655049-11655050	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs370955812	chr8:11655050-11655051	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs561480197	chr8:11655054-11655055	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs539640999	chr8:11655059-11655060	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs112959872	chr8:11655062-11655063	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs546918638	chr8:11655067-11655068	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs143948364	chr8:11655086-11655087	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs373768739	chr8:11655090-11655091	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs73207246	chr8:11655098-11655099	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs535157585	chr8:11655107-11655108	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs138000185	chr8:11655116-11655117	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs58165005	chr8:11655124-11655125	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs552985558	chr8:11655133-11655134	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs574357344	chr8:11655135-11655136	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs182762576	chr8:11655136-11655137	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs34350077	chr8:11655147-11655148	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs71700585	chr8:11655148-11655149	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs60716628	chr8:11655169-11655170	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs199772796	chr8:11655170-11655171	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:150)

Disease	PMID	Source
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	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
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
Congenital diaphragmatic hernia	21064195	CNVD
Autism	22495311	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Breast cancer	21990379	CNVD
Psoriasis	20403174	CNVD
Psoriasis	20663923	CNVD
Crohn''s disease	16909382	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Crohn''s disease	20877625	CNVD
Inflammatory disorder	20877625	CNVD
Cardiac defect	21933911	CNVD
Psoriasis	18059266	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Psoriasis	20877625	CNVD
Mental retardation	17847001	CNVD
Prostate cancer	17217626	CNVD
Schizophrenia	21399695	CNVD
Colorectal cancer	21128281	CNVD
Colorectal cancer	19455253	CNVD
Psoriasis	18848619	CNVD
Squamous cell cancer	19047905	CNVD
Colorectal cancer	17229543	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
Developmental disorder	20461109	CNVD
abnormal development	18461090	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioblastoma multiforme	21138945	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Gastric cancer	21811585	CNVD
Colorectal cancer	16774939	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cancer	20164919	CNVD
Gastric cancer	22315472	CNVD
Gastric cancer	17229543	CNVD
Disorders of sex development	22290220	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Honadal dysgenesis	21408189	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD

Chromatin state (count:1832 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:11628400-11656800	Weak transcription	Small Intestine	intestine
2	chr8:11636800-11659400	Weak transcription	Thymus	Thymus
3	chr8:11640800-11658600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
4	chr8:11641000-11658000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
5	chr8:11641000-11659600	Weak transcription	Right Atrium	heart
6	chr8:11641200-11658400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
7	chr8:11641200-11659000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
8	chr8:11643600-11658200	Weak transcription	Primary hematopoietic stem cells	blood
9	chr8:11643800-11659400	Weak transcription	Brain Angular Gyrus	brain
10	chr8:11643800-11659600	Weak transcription	Aorta	Aorta
11	chr8:11644200-11658400	Weak transcription	Brain Germinal Matrix	brain
12	chr8:11644400-11659400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
13	chr8:11644600-11659400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
14	chr8:11644800-11659000	Weak transcription	Primary T cells from cord blood	blood
15	chr8:11645000-11658600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr8:11645600-11654800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
17	chr8:11645600-11658200	Weak transcription	Primary B cells from cord blood	blood
18	chr8:11647400-11659400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr8:11647600-11656600	Weak transcription	Pancreas	Pancrea
20	chr8:11647600-11659400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr8:11647600-11659400	Weak transcription	Brain Inferior Temporal Lobe	brain
22	chr8:11647800-11657800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr8:11648000-11657800	Weak transcription	NHEK	skin
24	chr8:11648000-11658600	Weak transcription	Fetal Brain Female	brain
25	chr8:11652200-11658400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
26	chr8:11652800-11655200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr8:11653000-11654800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr8:11653000-11655000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr8:11653000-11655000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr8:11653000-11655000	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr8:11653000-11655000	Active TSS	NHDF-Ad	bronchial
32	chr8:11653400-11654800	Flanking Active TSS	HepG2	liver
33	chr8:11653400-11655400	Enhancers	Fetal Thymus	thymus
34	chr8:11653600-11655000	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
35	chr8:11653600-11655000	Enhancers	Monocytes-CD14+_RO01746	blood
36	chr8:11653800-11654800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr8:11653800-11654800	Enhancers	Primary monocytes fromperipheralblood	blood
38	chr8:11653800-11654800	Enhancers	Primary neutrophils fromperipheralblood	blood
39	chr8:11653800-11654800	Flanking Active TSS	Ovary	ovary
40	chr8:11653800-11654800	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
41	chr8:11653800-11654800	Enhancers	Sigmoid Colon	Sigmoid Colon
42	chr8:11653800-11655000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
43	chr8:11653800-11655400	Enhancers	Stomach Mucosa	stomach
44	chr8:11653800-11656200	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr8:11653800-11657000	Weak transcription	Fetal Intestine Small	intestine
46	chr8:11654000-11654800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr8:11654000-11654800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr8:11654000-11654800	Enhancers	Placenta	Placenta
49	chr8:11654000-11654800	Enhancers	GM12878-XiMat	blood
50	chr8:11654000-11655000	Flanking Active TSS	Colon Smooth Muscle	Colon

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