Variant report

Variant	nsv1028266
Chromosome Location	chr8:10537081-10586112
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:743)
CpG islands
(count:674)
Chromatin interactive
region (count:37)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:743 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:10573811-10574014	K562	blood:	n/a	n/a
2	ATF1	chr8:10556072-10556385	K562	blood:	n/a	n/a
3	ATF1	chr8:10568608-10568946	K562	blood:	n/a	n/a
4	ATF1	chr8:10547285-10547485	K562	blood:	n/a	n/a
5	ATF3	chr8:10538386-10538728	A549	lung:	n/a	n/a
6	ATF3	chr8:10556054-10556401	K562	blood:	n/a	n/a
7	BCL3	chr8:10538290-10538870	A549	lung:	n/a	n/a
8	BCL3	chr8:10538308-10538830	A549	lung:	n/a	n/a
9	BHLHE40	chr8:10572568-10572607	K562	blood:	n/a	n/a
10	BHLHE40	chr8:10568702-10568993	K562	blood:	n/a	n/a
11	BHLHE40	chr8:10548293-10549087	K562	blood:	n/a	chr8:10548805-10548821 chr8:10548940-10548956
12	BHLHE40	chr8:10547066-10547446	K562	blood:	n/a	n/a
13	BHLHE40	chr8:10537101-10537120	K562	blood:	n/a	n/a
14	BHLHE40	chr8:10556120-10556373	K562	blood:	n/a	n/a
15	BHLHE40	chr8:10574501-10574728	K562	blood:	n/a	n/a
16	BHLHE40	chr8:10573631-10574069	K562	blood:	n/a	n/a
17	BHLHE40	chr8:10584116-10584359	K562	blood:	n/a	n/a
18	BRCA1	chr8:10537000-10537113	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr8:10570054-10571623	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr8:10568658-10569027	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr8:10548322-10549104	Hela-S3	cervix:	n/a	n/a
22	BRCA1	chr8:10538366-10538794	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr8:10573807-10574032	Hela-S3	cervix:	n/a	n/a
24	CBX3	chr8:10573588-10574056	K562	blood:	n/a	n/a
25	CBX3	chr8:10560231-10560479	K562	blood:	n/a	n/a
26	CBX3	chr8:10548378-10548714	K562	blood:	n/a	n/a
27	CCNT2	chr8:10573634-10574186	K562	blood:	n/a	n/a
28	CEBPB	chr8:10556051-10556400	IMR90	lung:	n/a	chr8:10556221-10556232
29	CEBPB	chr8:10557100-10557263	K562	blood:	n/a	n/a
30	CEBPB	chr8:10544799-10544897	HepG2	liver:	n/a	chr8:10544848-10544859
31	CEBPB	chr8:10548379-10549212	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr8:10571432-10571595	HepG2	liver:	n/a	n/a
33	CEBPB	chr8:10556072-10556406	Hela-S3	cervix:	n/a	chr8:10556221-10556232
34	CEBPB	chr8:10563317-10563560	HepG2	liver:	n/a	n/a
35	CEBPB	chr8:10575751-10575883	K562	blood:	n/a	n/a
36	CEBPB	chr8:10556056-10556388	HepG2	liver:	n/a	chr8:10556221-10556232
37	CEBPB	chr8:10576835-10577013	K562	blood:	n/a	n/a
38	CEBPB	chr8:10570845-10571193	A549	lung:	n/a	n/a
39	CEBPB	chr8:10538263-10538912	A549	lung:	n/a	n/a
40	CEBPB	chr8:10538372-10538912	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr8:10563398-10563608	IMR90	lung:	n/a	n/a
42	CEBPB	chr8:10556053-10556413	K562	blood:	n/a	chr8:10556221-10556232
43	CEBPB	chr8:10556073-10556387	K562	blood:	n/a	chr8:10556221-10556232
44	CEBPB	chr8:10563484-10563575	K562	blood:	n/a	n/a
45	CEBPB	chr8:10570140-10571670	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr8:10570844-10571149	K562	blood:	n/a	n/a
47	CEBPB	chr8:10556061-10556406	A549	lung:	n/a	chr8:10556221-10556232
48	CEBPB	chr8:10556133-10556276	K562	blood:	n/a	chr8:10556221-10556232
49	CEBPB	chr8:10570897-10571105	HepG2	liver:	n/a	n/a
50	CEBPB	chr8:10568300-10569061	Hela-S3	cervix:	n/a	n/a

(count:674 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:10581988-10582038	K562	blood:	n/a
2	chr8:10581784-10581834	HRPEpiC	eye:	n/a
3	chr8:10558000-10558050	NH-A	brain:	n/a
4	chr8:10581988-10582038	K562	blood:	n/a
5	chr8:10581784-10581834	HRPEpiC	eye:	n/a
6	chr8:10558000-10558050	NH-A	brain:	n/a
7	chr8:10584169-10584219	NHDF-neo	bronchial:	n/a
8	chr8:10553728-10553778	PrEC	prostate:	n/a
9	chr8:10555466-10555516	HCM	heart:	n/a
10	chr8:10555382-10555432	U87	brain:	n/a
11	chr8:10581988-10582038	HRPEpiC	eye:	n/a
12	chr8:10558000-10558050	CMK	blood:	n/a
13	chr8:10583827-10583877	HCM	heart:	n/a
14	chr8:10583827-10583877	AG09309	skin:	n/a
15	chr8:10583326-10583376	GM19239	blood:	n/a
16	chr8:10583326-10583376	HepG2	liver:	n/a
17	chr8:10583326-10583376	HCT-116	colon:	n/a
18	chr8:10581784-10581834	LNCaP	prostate:	n/a
19	chr8:10583326-10583376	HUVEC	blood vessel:	n/a
20	chr8:10555382-10555432	HEEpiC	esophagus:	n/a
21	chr8:10581988-10582038	AG09309	skin:	n/a
22	chr8:10581784-10581834	SK-N-SH_RA	brain:	n/a
23	chr8:10555466-10555516	GM06990	blood:	n/a
24	chr8:10573804-10573854	SAEC	small airway:	n/a
25	chr8:10555382-10555432	Hepatocyte	liver:	n/a
26	chr8:10584169-10584219	HepG2	liver:	n/a
27	chr8:10555382-10555432	AG10803	skin:	n/a
28	chr8:10573804-10573854	HEK293	kidney:	embryo
29	chr8:10555382-10555432	HPAEpiC	pulmonary alveolar:	n/a
30	chr8:10583827-10583877	MCF10A-Er-Src	breast:	n/a
31	chr8:10581988-10582038	Jurkat	blood:	n/a
32	chr8:10585394-10585444	Hela-S3	cervix:	n/a
33	chr8:10581988-10582038	GM12892	blood:	n/a
34	chr8:10555466-10555516	HCF	heart:	n/a
35	chr8:10584169-10584219	PFSK-1	brain:	n/a
36	chr8:10581988-10582038	AG09319	gingival:	n/a
37	chr8:10583326-10583376	GM12878	blood:	n/a
38	chr8:10581988-10582038	NH-A	brain:	n/a
39	chr8:10553728-10553778	ovcar-3	ovarian:	n/a
40	chr8:10555466-10555516	PFSK-1	brain:	n/a
41	chr8:10555466-10555516	GM19239	blood:	n/a
42	chr8:10583827-10583877	PrEC	prostate:	n/a
43	chr8:10581784-10581834	HRE	kidney:	n/a
44	chr8:10573804-10573854	GM19239	blood:	n/a
45	chr8:10581988-10582038	U87	brain:	n/a
46	chr8:10555382-10555432	AG04450	lung:	fetal
47	chr8:10584169-10584219	U87	brain:	n/a
48	chr8:10584169-10584219	T-47D	breast:	n/a
49	chr8:10585394-10585444	SAEC	small airway:	n/a
50	chr8:10581988-10582038	ovcar-3	ovarian:	n/a

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:10573494..10575019-chr8:10578805..10581206,2	K562	blood:
2	chr8:10572945..10574994-chr8:10579706..10582412,2	K562	blood:
3	chr8:10501933..10503647-chr8:10579530..10582148,2	K562	blood:
4	chr8:10564366..10566017-chr8:10568811..10571288,2	K562	blood:
5	chr8:10582499..10584929-chr8:10712844..10715124,2	K562	blood:
6	chr8:10549207..10552160-chr8:10577938..10579847,2	K562	blood:
7	chr8:10447691..10448293-chr8:10586014..10586821,3	MCF-7	breast:
8	chr8:10539212..10540819-chr8:10542466..10545338,2	K562	blood:
9	chr8:10555796..10558370-chr8:10558494..10560524,2	K562	blood:
10	chr8:10556318..10558383-chr8:10558421..10560305,2	MCF-7	breast:
11	chr8:10561128..10563766-chr8:10580957..10583552,2	K562	blood:
12	chr8:10561879..10564186-chr8:10576793..10578956,2	K562	blood:
13	chr8:10582500..10584094-chr8:10592919..10595783,2	K562	blood:
14	chr8:10583182..10585584-chr8:10585920..10587606,2	K562	blood:
15	chr8:10561879..10564186-chr8:10576793..10578956,2	K562	blood:
16	chr8:10535340..10537589-chr8:10540581..10542267,2	K562	blood:
17	chr19:16180029..16180673-chr8:10548540..10549342,2	Hela-S3	cervix:
18	chr8:10534702..10537389-chr8:10561883..10564793,2	K562	blood:
19	chr8:10556097..10559916-chr8:10561605..10564138,3	K562	blood:
20	chr8:10556097..10559916-chr8:10561605..10564138,3	K562	blood:
21	chr8:10553523..10556097-chr8:10561265..10564003,2	K562	blood:
22	chr8:10572945..10574994-chr8:10579706..10582412,2	K562	blood:
23	chr8:10563640..10566502-chr8:10586406..10589328,2	K562	blood:
24	chr8:10553813..10555777-chr8:10556607..10558383,2	K562	blood:
25	chr8:10534702..10537389-chr8:10561883..10564793,2	K562	blood:
26	chr8:10537022..10539383-chr8:10695484..10697412,2	K562	blood:
27	chr8:10535340..10537589-chr8:10540581..10542267,2	K562	blood:
28	chr8:10553813..10555777-chr8:10556607..10558383,2	K562	blood:
29	chr8:10555796..10558370-chr8:10558494..10560524,2	K562	blood:
30	chr8:10573494..10575019-chr8:10578805..10581206,2	K562	blood:
31	chr8:10556318..10558383-chr8:10558421..10560305,2	MCF-7	breast:
32	chr8:10568215..10570516-chr8:10570791..10574753,3	K562	blood:
33	chr8:10553523..10556097-chr8:10561265..10564003,2	K562	blood:
34	chr8:10581535..10584414-chr8:10592948..10594895,2	MCF-7	breast:
35	chr8:10561128..10563766-chr8:10580957..10583552,2	K562	blood:
36	chr8:10539212..10541927-chr8:10542466..10544181,2	K562	blood:
37	chr8:10549207..10552160-chr8:10577938..10579847,2	K562	blood:

No data

Variant related genes	Relation type
RNA5SP252	TF binding region
RP1L1	TF binding region
ENSG00000248896	TF binding region
RNA5SP252	CpG island
RP1L1	CpG island
ENSG00000248896	CpG island
ENSG00000171056	chromatin interactions
ENSG00000212433	chromatin interactions
ENSG00000254093	chromatin interactions
ENSG00000183638	chromatin interactions
ENSG00000248896	chromatin interactions
ENSG00000258724	chromatin interactions

Extended variants
information (count: 2904 )
Associated
traits (count: 138 )

Variant overlapped rSNPs/rCNVs (count:2904 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs558368151	chr8:10537107-10537108	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs571798387	chr8:10537116-10537117	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs537515726	chr8:10537152-10537153	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs557409834	chr8:10537153-10537154	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs76233623	chr8:10537154-10537155	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs374019181	chr8:10537192-10537193	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs148920182	chr8:10537256-10537257	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs371795166	chr8:10537266-10537267	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs573036649	chr8:10537267-10537268	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs4240665	chr8:10537285-10537286	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs371445584	chr8:10537289-10537290	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs145639710	chr8:10537306-10537307	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs543862399	chr8:10537312-10537313	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs555277290	chr8:10537326-10537327	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs529740596	chr8:10537335-10537336	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs546268685	chr8:10537352-10537353	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs566397996	chr8:10537353-10537354	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs528773584	chr8:10537356-10537357	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs552027427	chr8:10537363-10537364	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs184267772	chr8:10537398-10537399	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs537554059	chr8:10537399-10537400	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs557380540	chr8:10537430-10537431	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs138314911	chr8:10537440-10537441	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs190427000	chr8:10537452-10537453	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs141319046	chr8:10537461-10537462	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs374451348	chr8:10537464-10537465	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs554964250	chr8:10537471-10537472	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs574726201	chr8:10537487-10537488	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs558338404	chr8:10537488-10537489	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs372730555	chr8:10537493-10537494	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs543998384	chr8:10537511-10537512	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs561078047	chr8:10537543-10537544	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs114327019	chr8:10537545-10537546	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs7009056	chr8:10537591-10537592	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs540250759	chr8:10537592-10537593	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs368465939	chr8:10537604-10537605	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs537664615	chr8:10537619-10537620	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs117178667	chr8:10537635-10537636	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs528812281	chr8:10537645-10537646	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs552064482	chr8:10537671-10537672	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs565485170	chr8:10537681-10537682	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs182570844	chr8:10537683-10537684	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs187176534	chr8:10537694-10537695	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs543922693	chr8:10537700-10537701	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs189058336	chr8:10537708-10537709	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs536318835	chr8:10537721-10537722	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs4841420	chr8:10537734-10537735	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs566486049	chr8:10537758-10537759	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs369139750	chr8:10537796-10537797	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs538547661	chr8:10537799-10537800	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:138)

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
Pancreatic ductal adenocarcinoma	19077451	CNVD
Gastric cancer	21811585	CNVD
Colorectal cancer	16774939	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:10526800-10537600	Weak transcription	Gastric	stomach
2	chr8:10530800-10537200	Weak transcription	Lung	lung
3	chr8:10533200-10538200	Weak transcription	Pancreas	Pancrea
4	chr8:10534800-10537600	Weak transcription	HUVEC	blood vessel
5	chr8:10536000-10538000	Enhancers	A549	lung
6	chr8:10536200-10540600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
7	chr8:10536400-10537800	Enhancers	Duodenum Mucosa	Duodenum
8	chr8:10536800-10537600	Enhancers	Fetal Muscle Leg	muscle
9	chr8:10536800-10539000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr8:10536800-10539200	Enhancers	NHEK	skin
11	chr8:10536800-10541800	Enhancers	Spleen	Spleen
12	chr8:10537000-10537400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr8:10537000-10537600	Enhancers	Fetal Muscle Trunk	muscle
14	chr8:10537000-10539000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr8:10537000-10539200	Flanking Active TSS	Hela-S3	cervix
16	chr8:10537000-10542000	Enhancers	Esophagus	oesophagus
17	chr8:10537200-10537400	Enhancers	Lung	lung
18	chr8:10537400-10538000	Weak transcription	Lung	lung
19	chr8:10537600-10538600	Weak transcription	Fetal Muscle Leg	muscle
20	chr8:10537600-10539400	Enhancers	HUVEC	blood vessel
21	chr8:10537600-10539600	Enhancers	Gastric	stomach
22	chr8:10537800-10538200	Bivalent Enhancer	Duodenum Mucosa	Duodenum
23	chr8:10537800-10539000	Enhancers	Liver	Liver
24	chr8:10537800-10539200	Enhancers	Brain Germinal Matrix	brain
25	chr8:10538000-10539000	Enhancers	NH-A	brain
26	chr8:10538000-10539200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr8:10538000-10539200	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
28	chr8:10538000-10539200	Bivalent Enhancer	Stomach Mucosa	stomach
29	chr8:10538000-10539200	Flanking Active TSS	A549	lung
30	chr8:10538000-10539400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr8:10538000-10539400	Enhancers	HMEC	breast
32	chr8:10538000-10539600	Enhancers	Breast Myoepithelial Primary Cells	Breast
33	chr8:10538000-10539800	Enhancers	Lung	lung
34	chr8:10538200-10538800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr8:10538200-10539200	Enhancers	Duodenum Mucosa	Duodenum
36	chr8:10538200-10540200	Enhancers	Pancreas	Pancrea
37	chr8:10538400-10538600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr8:10538400-10538800	Bivalent Enhancer	Stomach Smooth Muscle	stomach
39	chr8:10538600-10538800	Enhancers	Fetal Muscle Leg	muscle
40	chr8:10538600-10539000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
41	chr8:10539000-10539400	Bivalent Enhancer	Right Ventricle	heart
42	chr8:10539000-10542800	Weak transcription	Liver	Liver
43	chr8:10539200-10539400	Enhancers	Stomach Mucosa	stomach
44	chr8:10539200-10539600	Enhancers	A549	lung
45	chr8:10539200-10540200	Enhancers	Hela-S3	cervix
46	chr8:10539400-10540400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr8:10539400-10541400	Weak transcription	HUVEC	blood vessel
48	chr8:10540200-10541400	Weak transcription	Pancreas	Pancrea
49	chr8:10540400-10541000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr8:10540800-10541600	Enhancers	Lung	lung

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