Variant report

Variant	nsv890363
Chromosome Location	chr8:11647941-11681825
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1407)
CpG islands
(count:1711)
Chromatin interactive
region (count:52)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1407 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:11670385-11670535	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:11657809-11657977	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:11656441-11656736	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:11660241-11660402	HepG2	liver:	n/a	n/a
5	ARID3A	chr8:11660655-11661419	K562	blood:	n/a	n/a
6	ARID3A	chr8:11659794-11660028	HepG2	liver:	n/a	n/a
7	ARID3A	chr8:11666175-11666691	HepG2	liver:	n/a	n/a
8	ARID3A	chr8:11659764-11660172	K562	blood:	n/a	n/a
9	ARID3A	chr8:11656609-11656929	K562	blood:	n/a	n/a
10	ARID3A	chr8:11671599-11671984	HepG2	liver:	n/a	n/a
11	ATF1	chr8:11656586-11657065	K562	blood:	n/a	n/a
12	ATF1	chr8:11677780-11678103	K562	blood:	n/a	n/a
13	ATF2	chr8:11659666-11660052	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr8:11659730-11660126	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr8:11660680-11660740	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr8:11662812-11663108	K562	blood:	n/a	n/a
17	BACH1	chr8:11671211-11671244	K562	blood:	n/a	n/a
18	BACH1	chr8:11666079-11666400	H1-hESC	embryonic stem cell:	n/a	n/a
19	BATF	chr8:11656623-11656908	GM12878	blood:	n/a	n/a
20	BCL3	chr8:11659384-11660037	A549	lung:	n/a	n/a
21	BCLAF1	chr8:11661566-11662077	GM12878	blood:	n/a	n/a
22	BHLHE40	chr8:11663658-11663946	K562	blood:	n/a	n/a
23	BHLHE40	chr8:11657867-11657948	GM12878	blood:	n/a	n/a
24	BHLHE40	chr8:11653754-11654196	K562	blood:	n/a	n/a
25	BHLHE40	chr8:11662425-11662689	HepG2	liver:	n/a	n/a
26	BHLHE40	chr8:11661246-11661368	GM12878	blood:	n/a	n/a
27	BHLHE40	chr8:11656691-11657024	K562	blood:	n/a	n/a
28	BHLHE40	chr8:11659789-11660403	GM12878	blood:	n/a	chr8:11660162-11660178 chr8:11660194-11660210
29	BHLHE40	chr8:11659800-11661056	K562	blood:	n/a	chr8:11660162-11660178 chr8:11660194-11660210
30	BHLHE40	chr8:11662365-11662751	K562	blood:	n/a	n/a
31	BHLHE40	chr8:11677905-11678135	K562	blood:	n/a	n/a
32	BHLHE40	chr8:11662399-11662624	GM12878	blood:	n/a	n/a
33	BHLHE40	chr8:11654927-11655030	K562	blood:	n/a	n/a
34	BRCA1	chr8:11666148-11666197	H1-hESC	embryonic stem cell:	n/a	n/a
35	BRCA1	chr8:11659771-11660279	Hela-S3	cervix:	n/a	n/a
36	BRCA1	chr8:11665673-11665862	HepG2	liver:	n/a	n/a
37	BRCA1	chr8:11660658-11661794	Hela-S3	cervix:	n/a	n/a
38	BRCA1	chr8:11660295-11660433	HepG2	liver:	n/a	n/a
39	CBX3	chr8:11659675-11660453	K562	blood:	n/a	n/a
40	CCNT2	chr8:11659631-11661355	K562	blood:	n/a	n/a
41	CCNT2	chr8:11662396-11662576	K562	blood:	n/a	n/a
42	CCNT2	chr8:11665622-11666304	K562	blood:	n/a	n/a
43	CCNT2	chr8:11653668-11654277	K562	blood:	n/a	n/a
44	CEBPB	chr8:11659730-11659942	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr8:11668154-11668335	A549	lung:	n/a	chr8:11668261-11668272 chr8:11668260-11668273
46	CEBPB	chr8:11663260-11663546	HepG2	liver:	n/a	n/a
47	CEBPB	chr8:11671371-11672046	Hela-S3	cervix:	n/a	chr8:11671891-11671902
48	CEBPB	chr8:11657698-11658031	HepG2	liver:	n/a	n/a
49	CEBPB	chr8:11671740-11671945	H1-hESC	embryonic stem cell:	n/a	chr8:11671891-11671902
50	CEBPB	chr8:11653677-11653939	HepG2	liver:	n/a	n/a

(count:1711 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:11653368-11653418	ProgFib	skin:	n/a
2	chr8:11665962-11666012	HPAEpiC	pulmonary alveolar:	n/a
3	chr8:11656692-11656742	NH-A	brain:	n/a
4	chr8:11653368-11653418	ProgFib	skin:	n/a
5	chr8:11665962-11666012	HPAEpiC	pulmonary alveolar:	n/a
6	chr8:11656692-11656742	NH-A	brain:	n/a
7	chr8:11653368-11653418	SKMC	muscle:	n/a
8	chr8:11653276-11653326	K562	blood:	n/a
9	chr8:11665969-11666019	K562	blood:	n/a
10	chr8:11660733-11660783	GM06990	blood:	n/a
11	chr8:11660733-11660783	GM19239	blood:	n/a
12	chr8:11660733-11660783	ECC-1	luminal epithelium:	n/a
13	chr8:11660733-11660783	K562	blood:	n/a
14	chr8:11660924-11660974	Caco-2	colon:	n/a
15	chr8:11668491-11668541	IMR90	lung:	fetal
16	chr8:11660614-11660664	HEEpiC	esophagus:	n/a
17	chr8:11663584-11663634	ProgFib	skin:	n/a
18	chr8:11652174-11652224	AG04450	lung:	fetal
19	chr8:11660109-11660159	AG09319	gingival:	n/a
20	chr8:11656692-11656742	AG04450	lung:	fetal
21	chr8:11660030-11660080	ProgFib	skin:	n/a
22	chr8:11652174-11652224	AG10803	skin:	n/a
23	chr8:11663584-11663634	PFSK-1	brain:	n/a
24	chr8:11660924-11660974	ovcar-3	ovarian:	n/a
25	chr8:11665962-11666012	IMR90	lung:	fetal
26	chr8:11660061-11660111	SAEC	small airway:	n/a
27	chr8:11664728-11664778	BE2_C	brain:	n/a
28	chr8:11666017-11666067	HPAEpiC	pulmonary alveolar:	n/a
29	chr8:11653368-11653418	AG09319	gingival:	n/a
30	chr8:11660614-11660664	AG09309	skin:	n/a
31	chr8:11665962-11666012	HRE	kidney:	n/a
32	chr8:11665843-11665893	AG09319	gingival:	n/a
33	chr8:11652356-11652406	HEK293	kidney:	embryo
34	chr8:11660089-11660139	HepG2	liver:	n/a
35	chr8:11653276-11653326	BJ	skin:	n/a
36	chr8:11653276-11653326	PFSK-1	brain:	n/a
37	chr8:11656692-11656742	HRPEpiC	eye:	n/a
38	chr8:11660109-11660159	NHBE	bronchial:	n/a
39	chr8:11653435-11653485	HAEpiC	amniotic membrane:	n/a
40	chr8:11659497-11659547	HIPEpiC	eye:	n/a
41	chr8:11665843-11665893	MCF10A-Er-Src	breast:	n/a
42	chr8:11656692-11656742	T-47D	breast:	n/a
43	chr8:11670382-11670432	AG09309	skin:	n/a
44	chr8:11665969-11666019	GM12878	blood:	n/a
45	chr8:11666017-11666067	GM06990	blood:	n/a
46	chr8:11679319-11679369	GM12878	blood:	n/a
47	chr8:11666485-11666535	PANC-1	pancreas:	n/a
48	chr8:11653435-11653485	MCF10A-Er-Src	breast:	n/a
49	chr8:11653276-11653326	HCM	heart:	n/a
50	chr8:11663584-11663634	HCM	heart:	n/a

(count:52 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:11653120..11657894-chr8:11659261..11661744,5	K562	blood:
2	chr8:11648977..11652066-chr8:11653536..11656484,3	MCF-7	breast:
3	chr8:11618295..11620623-chr8:11664020..11665628,2	K562	blood:
4	chr8:11652587..11657894-chr8:11658127..11661459,7	K562	blood:
5	chr8:11647279..11650078-chr8:11653979..11656723,2	MCF-7	breast:
6	chr8:11658864..11661745-chr8:11724576..11726431,3	MCF-7	breast:
7	chr8:11659663..11662114-chr8:11670043..11672183,2	K562	blood:
8	chr6:30029044..30029552-chr8:11659926..11660449,2	HCT-116	colon:
9	chr8:11625684..11627765-chr8:11645905..11648269,2	K562	blood:
10	chr8:11626596..11628658-chr8:11659514..11662088,3	K562	blood:
11	chr8:11663591..11666285-chr8:11668539..11672798,5	K562	blood:
12	chr8:11657053..11659855-chr8:11661482..11664070,3	K562	blood:
13	chr8:11662802..11665653-chr8:11685244..11688002,2	K562	blood:
14	chr8:11658229..11662389-chr8:11662980..11669380,10	MCF-7	breast:
15	chr8:11645433..11648215-chr8:11658187..11661640,5	MCF-7	breast:
16	chr8:11660132..11662159-chr8:11687088..11688698,2	MCF-7	breast:
17	chr8:11663695..11667740-chr8:11686501..11689379,3	MCF-7	breast:
18	chr8:11662199..11664746-chr8:11796348..11798802,2	K562	blood:
19	chr17:41465211..41466190-chr8:11659722..11660251,2	Hela-S3	cervix:
20	chr8:11649932..11653064-chr8:11653128..11655366,3	K562	blood:
21	chr8:11652587..11657894-chr8:11658127..11661459,7	K562	blood:
22	chr11:2398309..2399006-chr8:11659548..11660515,2	HCT-116	colon:
23	chr8:11650636..11652578-chr8:11653838..11655597,2	K562	blood:
24	chr8:11662566..11665636-chr8:11705504..11707081,3	K562	blood:
25	chr8:11658229..11662389-chr8:11662980..11669380,10	MCF-7	breast:
26	chr8:11645433..11648215-chr8:11658187..11661640,5	MCF-7	breast:
27	chr8:11658127..11661675-chr8:11664375..11667732,3	K562	blood:
28	chr8:11650636..11652578-chr8:11653838..11655597,2	K562	blood:
29	chr6:24666810..24667602-chr8:11659901..11660485,2	HCT-116	colon:
30	chr8:11625747..11629309-chr8:11658765..11661345,4	K562	blood:
31	chr8:11648977..11652066-chr8:11653536..11656484,3	MCF-7	breast:
32	chr10:52384254..52384940-chr8:11659944..11660800,2	NB4	blood:
33	chr8:11658330..11660255-chr8:11664033..11666074,2	MCF-7	breast:
34	chr8:11649932..11653064-chr8:11653128..11655366,3	K562	blood:
35	chr8:11666673..11669607-chr8:11678720..11681322,2	K562	blood:
36	chr8:11652965..11656305-chr8:11661939..11664556,3	K562	blood:
37	chr8:11653668..11656600-chr8:11658872..11661623,3	MCF-7	breast:
38	chr8:11650546..11652103-chr8:11660021..11661839,2	MCF-7	breast:
39	chr8:11678607..11680636-chr8:11724388..11726584,2	MCF-7	breast:
40	chr8:11647649..11650731-chr8:11658511..11661458,3	K562	blood:
41	chr8:11666673..11669607-chr8:11678720..11681322,2	K562	blood:
42	chr8:11643528..11645314-chr8:11650082..11652912,2	MCF-7	breast:
43	chr8:11665243..11667469-chr8:11710761..11712863,3	MCF-7	breast:
44	chr8:11625967..11628744-chr8:11645697..11648212,2	MCF-7	breast:
45	chr8:11664303..11666890-chr8:11705423..11707941,2	MCF-7	breast:
46	chr8:11624784..11628111-chr8:11660073..11663416,4	MCF-7	breast:
47	chr8:11644178..11646906-chr8:11648968..11651779,2	K562	blood:
48	chr8:11659426..11661474-chr8:11724613..11726870,3	MCF-7	breast:
49	chr8:11658127..11661675-chr8:11664375..11667732,3	K562	blood:
50	chr8:11658330..11660255-chr8:11664033..11666074,2	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	chr8:11659431-11660021	NONHSAT125085
4	lnc-RP11-297N6.4.1-1	chr8:11655437-11655656	NONHSAT125085

No data

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

Extended variants
information (count: 2760 )
Associated
traits (count: 150 )

Variant overlapped rSNPs/rCNVs (count:2760 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2101914	chr8:11647941-11647942	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs570291690	chr8:11647954-11647955	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs537614901	chr8:11648015-11648016	Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs187559853	chr8:11648036-11648037	Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs73207235	chr8:11648041-11648042	Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs538351727	chr8:11648047-11648048	Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs2088349	chr8:11648067-11648068	Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs1883019	chr8:11648080-11648081	Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs113201295	chr8:11648133-11648134	Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs536166868	chr8:11648156-11648157	Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs554413164	chr8:11648193-11648194	Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs60069371	chr8:11648210-11648211	Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs192253804	chr8:11648213-11648214	Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs2088348	chr8:11648224-11648225	Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs1883020	chr8:11648231-11648232	Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs541156779	chr8:11648240-11648241	Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs184316009	chr8:11648261-11648262	Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs573920169	chr8:11648272-11648273	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs188652420	chr8:11648353-11648354	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs181221171	chr8:11648364-11648365	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs67192594	chr8:11648371-11648372	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs184744818	chr8:11648377-11648378	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs189259372	chr8:11648379-11648380	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs180684349	chr8:11648397-11648398	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs10089013	chr8:11648408-11648409	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs538757131	chr8:11648419-11648420	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs148735091	chr8:11648435-11648436	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs565356188	chr8:11648436-11648437	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs563036365	chr8:11648450-11648451	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs535809582	chr8:11648451-11648452	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs554453992	chr8:11648463-11648464	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs371621691	chr8:11648486-11648487	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs375127643	chr8:11648498-11648499	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs141534460	chr8:11648517-11648518	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs558759729	chr8:11648542-11648543	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs576946663	chr8:11648550-11648551	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs13258488	chr8:11648590-11648591	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs147497973	chr8:11648656-11648657	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs2740442	chr8:11648659-11648660	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs544249827	chr8:11648667-11648668	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs563668418	chr8:11648687-11648688	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs531277233	chr8:11648721-11648722	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs2740443	chr8:11648722-11648723	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs2645448	chr8:11648726-11648727	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs2740444	chr8:11648789-11648790	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs117367178	chr8:11648869-11648870	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs2645447	chr8:11648874-11648875	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs547830843	chr8:11648877-11648878	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs186469276	chr8:11648878-11648879	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs550582205	chr8:11648884-11648885	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 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:2565 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:11628400-11653000	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr8:11628400-11656800	Weak transcription	Small Intestine	intestine
3	chr8:11636800-11659400	Weak transcription	Thymus	Thymus
4	chr8:11640800-11658600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
5	chr8:11641000-11658000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
6	chr8:11641000-11659600	Weak transcription	Right Atrium	heart
7	chr8:11641200-11658400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
8	chr8:11641200-11659000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
9	chr8:11641400-11648600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr8:11641600-11653600	Weak transcription	Monocytes-CD14+_RO01746	blood
11	chr8:11641800-11653200	Weak transcription	Stomach Mucosa	stomach
12	chr8:11642000-11654200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr8:11642200-11653000	Weak transcription	Muscle Satellite Cultured Cells	--
14	chr8:11642600-11652800	Weak transcription	Colon Smooth Muscle	Colon
15	chr8:11643000-11653000	Weak transcription	Rectal Smooth Muscle	rectum
16	chr8:11643400-11653000	Weak transcription	Fetal Kidney	kidney
17	chr8:11643400-11653000	Weak transcription	HSMM	muscle
18	chr8:11643600-11658200	Weak transcription	Primary hematopoietic stem cells	blood
19	chr8:11643800-11653000	Weak transcription	Fetal Intestine Large	intestine
20	chr8:11643800-11653800	Weak transcription	Sigmoid Colon	Sigmoid Colon
21	chr8:11643800-11654000	Weak transcription	GM12878-XiMat	blood
22	chr8:11643800-11654400	Weak transcription	Gastric	stomach
23	chr8:11643800-11659400	Weak transcription	Brain Angular Gyrus	brain
24	chr8:11643800-11659600	Weak transcription	Aorta	Aorta
25	chr8:11644000-11648400	Weak transcription	Adipose Nuclei	Adipose
26	chr8:11644000-11653000	Weak transcription	Rectal Mucosa Donor 29	rectum
27	chr8:11644200-11653000	Weak transcription	Duodenum Smooth Muscle	Duodenum
28	chr8:11644200-11653200	Weak transcription	Colonic Mucosa	Colon
29	chr8:11644200-11658400	Weak transcription	Brain Germinal Matrix	brain
30	chr8:11644400-11648200	Weak transcription	Primary T cells fromperipheralblood	blood
31	chr8:11644400-11648200	Weak transcription	A549	lung
32	chr8:11644400-11648800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
33	chr8:11644400-11653000	Weak transcription	Duodenum Mucosa	Duodenum
34	chr8:11644400-11659400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
35	chr8:11644600-11648600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
36	chr8:11644600-11653000	Weak transcription	Placenta	Placenta
37	chr8:11644600-11654600	Weak transcription	Lung	lung
38	chr8:11644600-11654600	Weak transcription	Spleen	Spleen
39	chr8:11644600-11659400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
40	chr8:11644800-11648800	Weak transcription	Liver	Liver
41	chr8:11644800-11649400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
42	chr8:11644800-11654000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr8:11644800-11659000	Weak transcription	Primary T cells from cord blood	blood
44	chr8:11645000-11649600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
45	chr8:11645000-11650200	Weak transcription	Primary T helper cells PMA-I stimulated	--
46	chr8:11645000-11654000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr8:11645000-11658600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr8:11645200-11654400	Weak transcription	Primary T helper cells fromperipheralblood	blood
49	chr8:11645400-11648000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr8:11645600-11652800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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