Variant report

Variant	nsv890350
Chromosome Location	chr8:10305317-10346588
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:10318722-10318795	K562	blood:	n/a	n/a
2	CEBPB	chr8:10310668-10310999	HepG2	liver:	n/a	n/a
3	CEBPB	chr8:10310563-10310956	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr8:10310657-10310992	IMR90	lung:	n/a	n/a
5	CEBPB	chr8:10310687-10310906	K562	blood:	n/a	n/a
6	CTCF	chr8:10332004-10332128	GM12878	blood:	n/a	chr8:10332039-10332057 chr8:10332045-10332054 chr8:10332040-10332056 chr8:10332042-10332052 chr8:10332041-10332054
7	CTCF	chr8:10342504-10342668	Medullo	brain:	n/a	n/a
8	CTCF	chr8:10342500-10342650	NHDF-neo	bronchial:	n/a	n/a
9	CTCF	chr8:10342520-10342670	HMEC	breast:	n/a	n/a
10	CTCF	chr8:10331940-10332090	GM12874	blood:	n/a	chr8:10332039-10332057 chr8:10332045-10332054 chr8:10332040-10332056 chr8:10332042-10332052 chr8:10332041-10332054
11	CTCF	chr8:10331972-10332147	ProgFib	skin:	n/a	chr8:10332039-10332057 chr8:10332045-10332054 chr8:10332040-10332056 chr8:10332042-10332052 chr8:10332041-10332054
12	CTCF	chr8:10342500-10342650	BE2_C	brain:	n/a	n/a
13	CTCF	chr8:10332200-10332350	HFF	foreskin:	n/a	n/a
14	CTCF	chr8:10332080-10332230	WI-38	lung:	n/a	n/a
15	CTCF	chr8:10331880-10332030	WI-38	lung:	n/a	n/a
16	CTCF	chr8:10331980-10332130	GM12873	blood:	n/a	chr8:10332039-10332057 chr8:10332045-10332054 chr8:10332040-10332056 chr8:10332042-10332052 chr8:10332041-10332054
17	CTCF	chr8:10332000-10332150	GM12873	blood:	n/a	chr8:10332039-10332057 chr8:10332045-10332054 chr8:10332040-10332056 chr8:10332042-10332052 chr8:10332041-10332054
18	CTCF	chr8:10331940-10332090	WERI-Rb-1	eye:	n/a	chr8:10332039-10332057 chr8:10332045-10332054 chr8:10332040-10332056 chr8:10332042-10332052 chr8:10332041-10332054
19	CTCF	chr8:10332000-10332150	RPTEC	kidney:	n/a	chr8:10332039-10332057 chr8:10332045-10332054 chr8:10332040-10332056 chr8:10332042-10332052 chr8:10332041-10332054
20	CTCF	chr8:10331800-10331950	HFF	foreskin:	n/a	n/a
21	CTCF	chr8:10331960-10332110	AG04449	skin:	n/a	chr8:10332039-10332057 chr8:10332045-10332054 chr8:10332040-10332056 chr8:10332042-10332052 chr8:10332041-10332054
22	CTCF	chr8:10332000-10332150	HUVEC	blood vessel:	n/a	chr8:10332039-10332057 chr8:10332045-10332054 chr8:10332040-10332056 chr8:10332042-10332052 chr8:10332041-10332054
23	CTCF	chr8:10332020-10332170	HRPEpiC	eye:	n/a	chr8:10332039-10332057 chr8:10332045-10332054 chr8:10332040-10332056 chr8:10332042-10332052 chr8:10332041-10332054
24	CTCF	chr8:10331820-10331970	GM12864	blood:	n/a	n/a
25	CTCF	chr8:10330684-10330769	ProgFib	skin:	n/a	n/a
26	CTCF	chr8:10342547-10342638	LNCaP	prostate:	n/a	n/a
27	CTCF	chr8:10342605-10342617	Hela-S3	cervix:	n/a	n/a
28	CTCF	chr8:10330695-10330757	GM19239	blood:	n/a	n/a
29	CTCF	chr8:10331904-10332192	K562	blood:	n/a	chr8:10332039-10332057 chr8:10332045-10332054 chr8:10332040-10332056 chr8:10332042-10332052 chr8:10332041-10332054
30	CTCF	chr8:10342436-10342680	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr8:10332664-10332723	GM13977	blood:	n/a	n/a
32	CTCF	chr8:10331900-10332050	SAEC	small airway:	n/a	n/a
33	CTCF	chr8:10332040-10332190	GM06990	blood:	n/a	chr8:10332045-10332054 chr8:10332040-10332056 chr8:10332042-10332052 chr8:10332041-10332054
34	CTCF	chr8:10332020-10332170	NB4	blood:	n/a	chr8:10332039-10332057 chr8:10332045-10332054 chr8:10332040-10332056 chr8:10332042-10332052 chr8:10332041-10332054
35	CTCF	chr8:10342516-10342653	NHEK	skin:	n/a	n/a
36	CTCF	chr8:10331900-10332050	GM12871	blood:	n/a	n/a
37	CTCF	chr8:10342523-10342668	LNCaP	prostate:	n/a	n/a
38	CTCF	chr8:10342555-10342628	GM12892	blood:	n/a	n/a
39	CTCF	chr8:10331920-10332070	GM12869	blood:	n/a	chr8:10332039-10332057 chr8:10332045-10332054 chr8:10332040-10332056 chr8:10332042-10332052 chr8:10332041-10332054
40	CTCF	chr8:10331940-10332090	AG10803	skin:	n/a	chr8:10332039-10332057 chr8:10332045-10332054 chr8:10332040-10332056 chr8:10332042-10332052 chr8:10332041-10332054
41	CTCF	chr8:10331980-10332130	HepG2	liver:	n/a	chr8:10332039-10332057 chr8:10332045-10332054 chr8:10332040-10332056 chr8:10332042-10332052 chr8:10332041-10332054
42	CTCF	chr8:10331920-10332070	A549	lung:	n/a	chr8:10332039-10332057 chr8:10332045-10332054 chr8:10332040-10332056 chr8:10332042-10332052 chr8:10332041-10332054
43	CTCF	chr8:10331965-10332142	HepG2	liver:	n/a	chr8:10332039-10332057 chr8:10332045-10332054 chr8:10332040-10332056 chr8:10332042-10332052 chr8:10332041-10332054
44	CTCF	chr8:10331972-10332083	GM10266	blood:	n/a	chr8:10332039-10332057 chr8:10332045-10332054 chr8:10332040-10332056 chr8:10332042-10332052 chr8:10332041-10332054
45	CTCF	chr8:10342560-10342627	GM10266	blood:	n/a	n/a
46	CTCF	chr8:10342536-10342638	MCF-7	breast:	n/a	n/a
47	CTCF	chr8:10331960-10332110	HMF	breast:	n/a	chr8:10332039-10332057 chr8:10332045-10332054 chr8:10332040-10332056 chr8:10332042-10332052 chr8:10332041-10332054
48	CTCF	chr8:10332020-10332170	HFF	foreskin:	n/a	chr8:10332039-10332057 chr8:10332045-10332054 chr8:10332040-10332056 chr8:10332042-10332052 chr8:10332041-10332054
49	CTCF	chr8:10342562-10342606	MCF-7	breast:	n/a	n/a
50	CTCF	chr8:10332000-10332150	HEK293	kidney:	n/a	chr8:10332039-10332057 chr8:10332045-10332054 chr8:10332040-10332056 chr8:10332042-10332052 chr8:10332041-10332054

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:10339410-10339460	SKMC	muscle:	n/a
2	chr8:10339410-10339460	HCM	heart:	n/a
3	chr8:10339449-10339499	AG09319	gingival:	n/a
4	chr8:10339449-10339499	HMEC	breast:	n/a
5	chr8:10339477-10339527	HRE	kidney:	n/a
6	chr8:10339449-10339499	AoSMC	blood vessel:	n/a
7	chr8:10339477-10339527	Hepatocyte	liver:	n/a
8	chr8:10339410-10339460	HCF	heart:	n/a
9	chr8:10339477-10339527	H1-hESC	embryonic stem cell:	embryo
10	chr8:10339449-10339499	Caco-2	colon:	n/a
11	chr8:10339410-10339460	AG09319	gingival:	n/a
12	chr8:10339449-10339499	PrEC	prostate:	n/a
13	chr8:10339477-10339527	U87	brain:	n/a
14	chr8:10339449-10339499	A549	lung:	n/a
15	chr8:10339410-10339460	MCF10A-Er-Src	breast:	n/a
16	chr8:10339449-10339499	Hela-S3	cervix:	n/a
17	chr8:10339449-10339499	NH-A	brain:	n/a
18	chr8:10339449-10339499	HEK293	kidney:	embryo
19	chr8:10339477-10339527	GM12878	blood:	n/a
20	chr8:10339449-10339499	MCF-7	breast:	n/a
21	chr8:10339449-10339499	AG04449	skin:	fetal
22	chr8:10339449-10339499	HCM	heart:	n/a
23	chr8:10339477-10339527	BE2_C	brain:	n/a
24	chr8:10339449-10339499	HCT-116	colon:	n/a
25	chr8:10339477-10339527	NB4	blood:	n/a
26	chr8:10339410-10339460	LNCaP	prostate:	n/a
27	chr8:10339410-10339460	IMR90	lung:	fetal
28	chr8:10339449-10339499	NHBE	bronchial:	n/a
29	chr8:10339449-10339499	Hepatocyte	liver:	n/a
30	chr8:10339449-10339499	HCPEpiC	choroid plexus:	n/a
31	chr8:10339477-10339527	HIPEpiC	eye:	n/a
32	chr8:10339410-10339460	AG04450	lung:	fetal
33	chr8:10339410-10339460	HAEpiC	amniotic membrane:	n/a
34	chr8:10339477-10339527	NHDF-neo	bronchial:	n/a
35	chr8:10339410-10339460	GM12878	blood:	n/a
36	chr8:10339449-10339499	HAEpiC	amniotic membrane:	n/a
37	chr8:10339449-10339499	GM12878	blood:	n/a
38	chr8:10339477-10339527	SK-N-SH_RA	brain:	n/a
39	chr8:10339477-10339527	Hela-S3	cervix:	n/a
40	chr8:10339477-10339527	IMR90	lung:	fetal
41	chr8:10339477-10339527	HPAEpiC	pulmonary alveolar:	n/a
42	chr8:10339410-10339460	HUVEC	blood vessel:	n/a
43	chr8:10339449-10339499	GM12891	blood:	n/a
44	chr8:10339477-10339527	SAEC	small airway:	n/a
45	chr8:10339410-10339460	HMEC	breast:	n/a
46	chr8:10339449-10339499	RPTEC	kidney:	n/a
47	chr8:10339477-10339527	HCF	heart:	n/a
48	chr8:10339477-10339527	HCM	heart:	n/a
49	chr8:10339477-10339527	HEEpiC	esophagus:	n/a
50	chr8:10339410-10339460	K562	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:10339831..10342686-chr8:10351596..10354401,2	K562	blood:
2	chr8:10302259..10303778-chr8:10306329..10308452,2	K562	blood:
3	chr8:10281970..10284229-chr8:10318464..10320467,2	K562	blood:
4	chr8:10300339..10303104-chr8:10303257..10306151,2	K562	blood:
5	chr8:10331191..10333383-chr8:10342162..10343803,2	K562	blood:
6	chr8:10306242..10308473-chr8:10310068..10312588,2	K562	blood:
7	chr8:10306242..10308473-chr8:10310068..10312588,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP1L1-2	chr8:10338909-10340741	NONHSAT124998
2	lnc-PRSS55-1	chr8:10342683-10343382	NONHSAT125000
3	lnc-RP1L1-3	chr8:10335001-10335291	ENSG00000253678
4	lnc-RP1L1-3	chr8:10336688-10336885	ENSG00000253678
5	lnc-PRSS55-1	chr8:10339371-10340804	NONHSAT124996
6	lnc-PRSS55-1	chr8:10339916-10340804	NONHSAT125000
7	lnc-PRSS55-1	chr8:10339371-10339484	ENSG00000253641
8	lnc-PRSS55-1	chr8:10334709-10334793	ENSG00000253641
9	lnc-PRSS55-1	chr8:10343339-10343382	NONHSAT124999
10	lnc-PRSS55-1	chr8:10335380-10335408	ENSG00000253641
11	lnc-PRSS55-1	chr8:10344317-10346944	NONHSAT125003
12	lnc-PRSS55-1	chr8:10344317-10347176	ENSG00000272505.1
13	lnc-MSRA-3	chr8:10328326-10328856	NONHSAT124989
14	lnc-RP1L1-2	chr8:10341597-10341613	ENSG00000253649.1
15	lnc-RP1L1-3	chr8:10336688-10336899	NONHSAT124992
16	lnc-PRSS55-1	chr8:10337649-10337702	ENSG00000253641
17	lnc-PRSS55-1	chr8:10337649-10337702	ENSG00000253641
18	lnc-PRSS55-1	chr8:10337671-10337702	NONHSAT124996
19	lnc-RP1L1-3	chr8:10334630-10335291	NONHSAT124992
20	lnc-PRSS55-1	chr8:10335271-10335408	ENSG00000253641
21	lnc-PRSS55-1	chr8:10339916-10340804	NONHSAT124999
22	lnc-PRSS55-1	chr8:10332075-10332141	ENSG00000253641
23	lnc-RP1L1-2	chr8:10340434-10340741	ENSG00000253649.1
24	lnc-PRSS55-1	chr8:10337649-10337702	ENSG00000253641
25	lnc-PRSS55-1	chr8:10334633-10334804	ENSG00000253641
26	lnc-RP1L1-2	chr8:10341708-10341756	ENSG00000253649.1
27	lnc-RP1L1-3	chr8:10336042-10336065	NONHSAT124995
28	lnc-PRSS55-1	chr8:10338056-10338496	ENSG00000253641
29	lnc-RP1L1-2	chr8:10341597-10342143	NONHSAT124998
30	lnc-MSRA-2	chr8:10305529-10308687	NONHSAT124988
31	lnc-PRSS55-1	chr8:10345921-10346428	NONHSAT124996
32	lnc-PRSS55-1	chr8:10338692-10338976	ENSG00000253641
33	lnc-RP1L1-3	chr8:10336688-10336899	NONHSAT124995
34	lnc-MSRA-3	chr8:10312147-10312190	NONHSAT124989
35	lnc-MSRA-2	chr8:10305072-10305433	NONHSAT124988
36	lnc-PRSS55-1	chr8:10335271-10335408	ENSG00000253641

Variant related genes	Relation type
ENSG00000253678	TF binding region
ENSG00000272505	TF binding region
RNU6-729P	TF binding region
ENSG00000253641	TF binding region
ENSG00000253678	CpG island
ENSG00000272505	CpG island
RNU6-729P	CpG island
ENSG00000253641	CpG island
ENSG00000253641	chromatin interactions

Extended variants
information (count: 2460 )
Associated
traits (count: 139 )

Variant overlapped rSNPs/rCNVs (count:2460 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10086673	chr8:10305317-10305318	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs550746644	chr8:10305336-10305337	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
3	rs143496577	chr8:10305348-10305349	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
4	rs7827718	chr8:10305353-10305354	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs560817617	chr8:10305360-10305361	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
6	rs574616167	chr8:10305377-10305378	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
7	rs35557634	chr8:10305384-10305385	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
8	rs557029620	chr8:10305415-10305416	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
9	rs115835794	chr8:10305431-10305432	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
10	rs536231500	chr8:10305512-10305513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs118105212	chr8:10305524-10305525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs543731745	chr8:10305530-10305531	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
13	rs573018458	chr8:10305531-10305532	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
14	rs10086909	chr8:10305532-10305533	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs558418221	chr8:10305568-10305569	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
16	rs575516866	chr8:10305603-10305604	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
17	rs188236156	chr8:10305642-10305643	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
18	rs182017200	chr8:10305648-10305649	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
19	rs529842911	chr8:10305710-10305711	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
20	rs563603773	chr8:10305716-10305717	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
21	rs560118085	chr8:10305724-10305725	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
22	rs528733423	chr8:10305734-10305735	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
23	rs552061282	chr8:10305738-10305739	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
24	rs116478195	chr8:10305740-10305741	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
25	rs115798395	chr8:10305754-10305755	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
26	rs148008589	chr8:10305771-10305772	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
27	rs567408638	chr8:10305840-10305841	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
28	rs536768227	chr8:10305843-10305844	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
29	rs186352884	chr8:10305845-10305846	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
30	rs189128349	chr8:10305867-10305868	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
31	rs532472040	chr8:10305868-10305869	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
32	rs552467588	chr8:10305872-10305873	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
33	rs538513831	chr8:10305880-10305881	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
34	rs558879523	chr8:10305892-10305893	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
35	rs373263536	chr8:10305915-10305916	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
36	rs575657153	chr8:10306014-10306015	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
37	rs181626557	chr8:10306016-10306017	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
38	rs186350241	chr8:10306042-10306043	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
39	rs574413161	chr8:10306098-10306099	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
40	rs540328108	chr8:10306108-10306109	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
41	rs547919382	chr8:10306124-10306125	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
42	rs567648305	chr8:10306132-10306133	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
43	rs191599798	chr8:10306154-10306155	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
44	rs559854647	chr8:10306229-10306230	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
45	rs182960125	chr8:10306230-10306231	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
46	rs7813610	chr8:10306244-10306245	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs565219522	chr8:10306290-10306291	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
48	rs531145628	chr8:10306293-10306294	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
49	rs550730486	chr8:10306305-10306306	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
50	rs374679352	chr8:10306308-10306309	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:139)

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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Epilepsy	20502679	CNVD
Osteosarcoma	21215367	CNVD
Gastric cancer	21811585	CNVD

Chromatin state (count:199 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:10292200-10321400	Weak transcription	Fetal Brain Male	brain
2	chr8:10294200-10306600	Weak transcription	Liver	Liver
3	chr8:10304400-10328200	Weak transcription	Fetal Brain Female	brain
4	chr8:10305400-10305600	Weak transcription	Pancreas	Pancrea
5	chr8:10308800-10314800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr8:10310800-10321000	Weak transcription	Pancreas	Pancrea
7	chr8:10312000-10312200	Enhancers	Duodenum Smooth Muscle	Duodenum
8	chr8:10312000-10312200	Enhancers	Fetal Lung	lung
9	chr8:10312200-10314000	Weak transcription	Fetal Lung	lung
10	chr8:10312400-10312800	Enhancers	Rectal Smooth Muscle	rectum
11	chr8:10312400-10313200	Weak transcription	Duodenum Smooth Muscle	Duodenum
12	chr8:10312600-10312800	Enhancers	Colon Smooth Muscle	Colon
13	chr8:10312800-10315000	Weak transcription	Cortex derived primary cultured neurospheres	brain
14	chr8:10313000-10317400	Weak transcription	Primary neutrophils fromperipheralblood	blood
15	chr8:10313200-10313400	Enhancers	Duodenum Smooth Muscle	Duodenum
16	chr8:10313400-10314000	Weak transcription	Duodenum Smooth Muscle	Duodenum
17	chr8:10313800-10315200	Enhancers	Stomach Mucosa	stomach
18	chr8:10314000-10314600	Enhancers	Adipose Nuclei	Adipose
19	chr8:10314000-10315400	Enhancers	Fetal Lung	lung
20	chr8:10314200-10314400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr8:10314200-10314400	Enhancers	Duodenum Smooth Muscle	Duodenum
22	chr8:10314200-10314600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr8:10314200-10314600	Enhancers	Esophagus	oesophagus
24	chr8:10314200-10314600	Enhancers	K562	blood
25	chr8:10314200-10314800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr8:10314200-10314800	Enhancers	Fetal Stomach	stomach
27	chr8:10314400-10315200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr8:10314800-10315400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr8:10315000-10315400	Strong transcription	Cortex derived primary cultured neurospheres	brain
30	chr8:10315200-10315600	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr8:10315200-10315600	ZNF genes & repeats	Aorta	Aorta
32	chr8:10315400-10318200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr8:10315400-10328400	Weak transcription	Cortex derived primary cultured neurospheres	brain
34	chr8:10315600-10321000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr8:10319200-10330600	Weak transcription	Gastric	stomach
36	chr8:10319600-10319800	ZNF genes & repeats	Brain Germinal Matrix	brain
37	chr8:10319800-10329400	Weak transcription	Brain Germinal Matrix	brain
38	chr8:10321000-10321200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr8:10321000-10321400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
40	chr8:10321400-10321600	Enhancers	Fetal Brain Male	brain
41	chr8:10322000-10335400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
42	chr8:10324000-10324400	Weak transcription	Liver	Liver
43	chr8:10324400-10324600	ZNF genes & repeats	Aorta	Aorta
44	chr8:10324600-10325600	Weak transcription	Aorta	Aorta
45	chr8:10324800-10325600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr8:10325000-10325200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr8:10325200-10330600	Weak transcription	Liver	Liver
48	chr8:10326000-10326200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr8:10326200-10336800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr8:10327000-10328200	Weak transcription	Aorta	Aorta

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