Variant report

Variant	nsv904120
Chromosome Location	chr15:42109975-42153085
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1008)
CpG islands
(count:1282)
Chromatin interactive
region (count:65)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1008 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr15:42120392-42120793	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr15:42119616-42119901	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr15:42120297-42120875	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr15:42120372-42120572	K562	blood:	n/a	n/a
5	BCL3	chr15:42119854-42120640	A549	lung:	n/a	n/a
6	BCL3	chr15:42119375-42120626	GM12878	blood:	n/a	n/a
7	BCL3	chr15:42119603-42120243	A549	lung:	n/a	n/a
8	BHLHE40	chr15:42125043-42125353	GM12878	blood:	n/a	n/a
9	BHLHE40	chr15:42120145-42120737	K562	blood:	n/a	n/a
10	BHLHE40	chr15:42152267-42152554	K562	blood:	n/a	n/a
11	BHLHE40	chr15:42118568-42118585	K562	blood:	n/a	n/a
12	BHLHE40	chr15:42140864-42141081	K562	blood:	n/a	n/a
13	BRCA1	chr15:42120259-42120593	Hela-S3	cervix:	n/a	n/a
14	CBX3	chr15:42120177-42120921	K562	blood:	n/a	n/a
15	CCNT2	chr15:42119621-42120692	K562	blood:	n/a	n/a
16	CEBPB	chr15:42142710-42143049	A549	lung:	n/a	n/a
17	CEBPB	chr15:42142481-42143077	K562	blood:	n/a	n/a
18	CEBPB	chr15:42120364-42120958	K562	blood:	n/a	n/a
19	CEBPB	chr15:42142668-42143076	MCF-7	breast:	n/a	n/a
20	CEBPB	chr15:42142786-42142940	K562	blood:	n/a	n/a
21	CEBPB	chr15:42124468-42124770	K562	blood:	n/a	chr15:42124601-42124612
22	CEBPB	chr15:42130435-42131103	ECC-1	luminal epithelium:	n/a	n/a
23	CEBPB	chr15:42130622-42130811	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr15:42130364-42131104	HCT-116	colon:	n/a	n/a
25	CEBPB	chr15:42124429-42124791	A549	lung:	n/a	chr15:42124601-42124612
26	CEBPB	chr15:42130423-42131080	MCF-7	breast:	n/a	n/a
27	CEBPB	chr15:42130634-42130834	K562	blood:	n/a	n/a
28	CEBPB	chr15:42117679-42117994	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr15:42130546-42130956	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr15:42130451-42130951	ECC-1	luminal epithelium:	n/a	n/a
31	CEBPB	chr15:42124523-42124799	MCF-7	breast:	n/a	chr15:42124601-42124612
32	CEBPB	chr15:42124464-42124722	K562	blood:	n/a	chr15:42124601-42124612
33	CEBPB	chr15:42142696-42143062	IMR90	lung:	n/a	n/a
34	CEBPB	chr15:42140879-42141129	IMR90	lung:	n/a	n/a
35	CEBPB	chr15:42124968-42125593	ECC-1	luminal epithelium:	n/a	n/a
36	CEBPB	chr15:42124921-42125585	ECC-1	luminal epithelium:	n/a	n/a
37	CEBPB	chr15:42120195-42121046	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr15:42149896-42150096	HepG2	liver:	n/a	n/a
39	CEBPB	chr15:42142720-42143068	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr15:42142646-42143071	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr15:42142620-42143113	ECC-1	luminal epithelium:	n/a	n/a
42	CEBPB	chr15:42130600-42130870	IMR90	lung:	n/a	n/a
43	CEBPB	chr15:42142741-42142962	HepG2	liver:	n/a	n/a
44	CEBPB	chr15:42130463-42131106	MCF-7	breast:	n/a	n/a
45	CEBPB	chr15:42130320-42131100	HCT-116	colon:	n/a	n/a
46	CEBPB	chr15:42142662-42143131	MCF-7	breast:	n/a	n/a
47	CEBPB	chr15:42142589-42143068	A549	lung:	n/a	n/a
48	CEBPB	chr15:42124423-42124790	HepG2	liver:	n/a	chr15:42124601-42124612
49	CEBPB	chr15:42130584-42130895	HepG2	liver:	n/a	n/a
50	CEBPB	chr15:42142652-42143048	K562	blood:	n/a	n/a

(count:1282 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:42118869-42118919	U87	brain:	n/a
2	chr15:42118869-42118919	U87	brain:	n/a
3	chr15:42129464-42129514	BJ	skin:	n/a
4	chr15:42140150-42140200	GM12891	blood:	n/a
5	chr15:42120681-42120731	AG09319	gingival:	n/a
6	chr15:42140715-42140765	SKMC	muscle:	n/a
7	chr15:42120087-42120137	NT2-D1	testis:	n/a
8	chr15:42141147-42141197	HRCEpiC	kidney:	n/a
9	chr15:42131658-42131708	HAEpiC	amniotic membrane:	n/a
10	chr15:42123717-42123767	AoSMC	blood vessel:	n/a
11	chr15:42120087-42120137	BE2_C	brain:	n/a
12	chr15:42140150-42140200	AG04450	lung:	fetal
13	chr15:42120681-42120731	IMR90	lung:	fetal
14	chr15:42119951-42120001	GM12892	blood:	n/a
15	chr15:42119864-42119914	Caco-2	colon:	n/a
16	chr15:42119864-42119914	Jurkat	blood:	n/a
17	chr15:42130735-42130785	HNPCEpiC	eye:	n/a
18	chr15:42119864-42119914	AG09319	gingival:	n/a
19	chr15:42120091-42120141	MCF10A-Er-Src	breast:	n/a
20	chr15:42120362-42120412	HepG2	liver:	n/a
21	chr15:42123717-42123767	HL-60	blood:	n/a
22	chr15:42130650-42130700	HepG2	liver:	n/a
23	chr15:42120087-42120137	ovcar-3	ovarian:	n/a
24	chr15:42129464-42129514	NT2-D1	testis:	n/a
25	chr15:42141147-42141197	HCT-116	colon:	n/a
26	chr15:42119951-42120001	T-47D	breast:	n/a
27	chr15:42130650-42130700	GM06990	blood:	n/a
28	chr15:42120681-42120731	HUVEC	blood vessel:	n/a
29	chr15:42131658-42131708	AG10803	skin:	n/a
30	chr15:42130650-42130700	RPTEC	kidney:	n/a
31	chr15:42140150-42140200	Hepatocyte	liver:	n/a
32	chr15:42120091-42120141	AG09319	gingival:	n/a
33	chr15:42120426-42120476	GM19239	blood:	n/a
34	chr15:42131658-42131708	HRE	kidney:	n/a
35	chr15:42131658-42131708	A549	lung:	n/a
36	chr15:42118869-42118919	IMR90	lung:	fetal
37	chr15:42120082-42120132	SK-N-SH_RA	brain:	n/a
38	chr15:42119684-42119734	HepG2	liver:	n/a
39	chr15:42123717-42123767	HIPEpiC	eye:	n/a
40	chr15:42141147-42141197	HUVEC	blood vessel:	n/a
41	chr15:42120087-42120137	HMEC	breast:	n/a
42	chr15:42120681-42120731	RPTEC	kidney:	n/a
43	chr15:42131658-42131708	NT2-D1	testis:	n/a
44	chr15:42120362-42120412	HUVEC	blood vessel:	n/a
45	chr15:42120082-42120132	T-47D	breast:	n/a
46	chr15:42131658-42131708	AG09309	skin:	n/a
47	chr15:42120091-42120141	Hepatocyte	liver:	n/a
48	chr15:42141147-42141197	LNCaP	prostate:	n/a
49	chr15:42120681-42120731	BJ	skin:	n/a
50	chr15:42130662-42130712	HCT-116	colon:	n/a

(count:65 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr15:42106913..42109055-chr15:42110591..42113388,3	K562	blood:
2	chr15:42144528..42146188-chr15:42157927..42160220,2	K562	blood:
3	chr15:42146846..42149806-chr15:42162512..42164389,2	K562	blood:
4	chr15:42119971..42120818-chr6:86387942..86388584,2	Hela-S3	cervix:
5	chr15:42105041..42106569-chr15:42108766..42110303,2	K562	blood:
6	chr15:41835700..41837704-chr15:42118864..42120391,2	K562	blood:
7	chr15:42116098..42118578-chr15:42118633..42120214,2	MCF-7	breast:
8	chr15:42127281..42132563-chr15:42140689..42145219,5	K562	blood:
9	chr15:42147889..42150225-chr15:42151669..42154619,2	MCF-7	breast:
10	chr15:42111390..42114154-chr15:42114914..42116415,2	K562	blood:
11	chr15:42128850..42133555-chr15:42135364..42139036,5	K562	blood:
12	chr15:42133144..42136683-chr15:42139373..42142777,4	K562	blood:
13	chr15:42121774..42125537-chr15:42128092..42132193,4	MCF-7	breast:
14	chr15:42120330..42121195-chr9:96212843..96213666,2	Hela-S3	cervix:
15	chr15:41851094..41853395-chr15:42110650..42112904,2	K562	blood:
16	chr15:42126911..42129447-chr15:42131730..42134137,2	MCF-7	breast:
17	chr15:42106183..42109859-chr15:42118195..42121802,3	K562	blood:
18	chr15:42133144..42136683-chr15:42139373..42142777,4	K562	blood:
19	chr15:42139809..42142475-chr15:42153474..42155142,2	MCF-7	breast:
20	chr15:42119169..42123691-chr15:42124459..42130624,7	MCF-7	breast:
21	chr15:42140186..42143232-chr15:42153052..42155732,3	K562	blood:
22	chr15:42147889..42150225-chr15:42151669..42154619,2	MCF-7	breast:
23	chr15:42116882..42118794-chr15:42146288..42147795,2	K562	blood:
24	chr15:42145763..42147692-chr15:42149451..42151046,2	K562	blood:
25	chr15:42134555..42137354-chr15:42142923..42146121,3	K562	blood:
26	chr15:42114563..42118600-chr15:42118704..42121383,3	K562	blood:
27	chr15:42121774..42125537-chr15:42128092..42132193,4	MCF-7	breast:
28	chr15:42129367..42131992-chr15:42144303..42147962,3	K562	blood:
29	chr15:42130359..42132534-chr15:42135770..42138086,2	K562	blood:
30	chr15:42151221..42156188-chr15:42156216..42158464,5	K562	blood:
31	chr15:42122872..42126047-chr15:42126791..42131021,4	K562	blood:
32	chr15:42127281..42132563-chr15:42140689..42145219,5	K562	blood:
33	chr15:42119178..42121855-chr15:42127765..42129934,4	K562	blood:
34	chr15:42065876..42068807-chr15:42118615..42122663,5	K562	blood:
35	chr15:42109699..42113332-chr15:42113557..42118168,5	K562	blood:
36	chr15:42119178..42121855-chr15:42127765..42129934,4	K562	blood:
37	chr15:42115008..42115577-chr15:42196451..42197341,2	MCF-7	breast:
38	chr15:42119641..42122495-chr15:42123255..42125312,3	K562	blood:
39	chr15:42119185..42121349-chr15:42128797..42131937,4	MCF-7	breast:
40	chr15:42125345..42127041-chr15:42137059..42139924,2	K562	blood:
41	chr15:42114988..42115997-chr15:42196197..42197506,6	MCF-7	breast:
42	chr15:42116882..42118794-chr15:42146288..42147795,2	K562	blood:
43	chr15:42126911..42129447-chr15:42131730..42134137,2	MCF-7	breast:
44	chr15:42119641..42122495-chr15:42123255..42125312,3	K562	blood:
45	chr15:42148229..42150660-chr15:42156373..42159189,2	K562	blood:
46	chr15:42119559..42121524-chr15:42137744..42139506,3	K562	blood:
47	chr15:42119185..42121349-chr15:42128797..42131937,4	MCF-7	breast:
48	chr15:42107512..42109083-chr15:42109246..42111016,2	MCF-7	breast:
49	chr15:41951879..41954479-chr15:42115654..42117641,2	K562	blood:
50	chr15:42148784..42150939-chr15:42202289..42204151,2	MCF-7	breast:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SPTBN5-1	chr15:42118224-42118517	ENSG00000250379.1
2	lnc-SPTBN5-1	chr15:42119835-42120053	ENSG00000250379.1
3	lnc-SPTBN5-1	chr15:42117297-42117571	ENSG00000250379.1
4	lnc-SPTBN5-1	chr15:42119935-42120134	ENSG00000250379.1
5	lnc-EHD4-1	chr15:42140569-42140826	NONHSAT041973
6	lnc-JMJD7-PLA2G4B-6	chr15:42111270-42111610	NONHSAT041965
7	lnc-EHD4-1	chr15:42142067-42142770	NONHSAT041973
8	lnc-JMJD7-PLA2G4B-6	chr15:42114848-42115420	NONHSAT041966
9	lnc-JMJD7-PLA2G4B-6	chr15:42115645-42115674	NONHSAT041966
10	lnc-SPTBN5-1	chr15:42118612-42118721	ENSG00000250379.1

No data

Variant related genes	Relation type
PLA2G4B	TF binding region
JMJD7-PLA2G4B	TF binding region
ENSG00000250379	TF binding region
MAPKBP1	TF binding region
SPTBN5	TF binding region
JMJD7	TF binding region
RNA5SP393	TF binding region
PLA2G4B	CpG island
JMJD7-PLA2G4B	CpG island
ENSG00000250379	CpG island
MAPKBP1	CpG island
SPTBN5	CpG island
JMJD7	CpG island
RNA5SP393	CpG island
ENSG00000231500	chromatin interactions
ENSG00000168970	chromatin interactions
ENSG00000188938	chromatin interactions
ENSG00000103966	chromatin interactions
ENSG00000137877	chromatin interactions
ENSG00000250379	chromatin interactions
ENSG00000243708	chromatin interactions
ENSG00000246740	chromatin interactions
ENSG00000103932	chromatin interactions
ENSG00000092445	chromatin interactions
ENSG00000174197	chromatin interactions
ENSG00000264850	chromatin interactions
ENSG00000200293	chromatin interactions
ENSG00000243789	chromatin interactions
ENSG00000223501	chromatin interactions
ENSG00000203875	chromatin interactions
ENSG00000137802	chromatin interactions

Extended variants
information (count: 2768 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:2768 , 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	rs2303518	chr15:42109975-42109976	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs189885527	chr15:42109978-42109979	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs534460170	chr15:42109981-42109982	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs200159876	chr15:42109982-42109983	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs372821195	chr15:42109984-42109985	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs180883655	chr15:42109993-42109994	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs539631658	chr15:42110012-42110013	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs556758666	chr15:42110045-42110046	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs373682432	chr15:42110081-42110082	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs576454048	chr15:42110117-42110118	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs541922364	chr15:42110156-42110157	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs375535175	chr15:42110173-42110174	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs369824432	chr15:42110175-42110176	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs368254621	chr15:42110194-42110195	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs139165608	chr15:42110272-42110273	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs201266812	chr15:42110274-42110275	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs149750128	chr15:42110276-42110277	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs368863760	chr15:42110297-42110298	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs201011586	chr15:42110304-42110305	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs532470910	chr15:42110320-42110321	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs369503982	chr15:42110335-42110336	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs112379544	chr15:42110347-42110348	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs371791061	chr15:42110362-42110363	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs374874546	chr15:42110381-42110382	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs370234123	chr15:42110383-42110384	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs373304967	chr15:42110386-42110387	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs377337993	chr15:42110421-42110422	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs148888745	chr15:42110475-42110476	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs369439925	chr15:42110486-42110487	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs113015793	chr15:42110493-42110494	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs376065390	chr15:42110525-42110526	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs201987753	chr15:42110550-42110551	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs370382274	chr15:42110553-42110554	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs144048924	chr15:42110639-42110640	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs374518727	chr15:42110697-42110698	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs568036665	chr15:42110725-42110726	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs150920206	chr15:42110783-42110784	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs3214532	chr15:42110817-42110818	Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs71474403	chr15:42110821-42110822	Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs371532334	chr15:42110830-42110831	Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs112099636	chr15:42110837-42110838	Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs184898601	chr15:42110847-42110848	Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs36102978	chr15:42110871-42110872	Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs571049585	chr15:42110961-42110962	Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs373858848	chr15:42110969-42110970	Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs374431801	chr15:42111073-42111074	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs534654016	chr15:42111074-42111075	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs540170901	chr15:42111088-42111089	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs199895922	chr15:42111095-42111096	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs61729964	chr15:42111100-42111101	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:69)

Disease	PMID	Source
HDAC8	0	CNVD
NIPBL	0	CNVD
RAD21	0	CNVD
SMC1A	0	CNVD
SMC3	0	CNVD
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Angelman syndrome	16183798	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16774939	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	20164920	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Cancer	21129771	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	21045282	CNVD
Breast cancer	22032731	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Multiple myeloma	16616336	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Myelofibrosis	22110671	CNVD
Maculopathy	20981449	CNVD
Gastric adenocarcinoma	19115996	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1808 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:42083800-42119400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr15:42089400-42114800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr15:42097200-42111000	Weak transcription	Fetal Kidney	kidney
4	chr15:42097800-42119600	Weak transcription	Psoas Muscle	Psoas
5	chr15:42098200-42118800	Strong transcription	Fetal Stomach	stomach
6	chr15:42098800-42115600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr15:42099000-42110000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
8	chr15:42099000-42110000	Weak transcription	Stomach Mucosa	stomach
9	chr15:42099200-42110000	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr15:42099200-42112000	Weak transcription	A549	lung
11	chr15:42100200-42113200	Strong transcription	Fetal Intestine Small	intestine
12	chr15:42100800-42118800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
13	chr15:42101800-42119000	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr15:42101800-42119600	Weak transcription	Hela-S3	cervix
15	chr15:42102000-42113000	Strong transcription	Fetal Intestine Large	intestine
16	chr15:42102000-42118600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr15:42103200-42112800	Strong transcription	Gastric	stomach
18	chr15:42103200-42118200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr15:42103600-42110400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
20	chr15:42103600-42111000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr15:42103600-42114000	Strong transcription	Esophagus	oesophagus
22	chr15:42103600-42116600	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr15:42103600-42117400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr15:42103600-42118200	Strong transcription	Placenta	Placenta
25	chr15:42103600-42118200	Strong transcription	NHEK	skin
26	chr15:42103600-42118800	Strong transcription	Spleen	Spleen
27	chr15:42103800-42118000	Strong transcription	Brain Anterior Caudate	brain
28	chr15:42103800-42118800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr15:42103800-42118800	Strong transcription	HMEC	breast
30	chr15:42104000-42113000	Strong transcription	Osteobl	bone
31	chr15:42104000-42117000	Weak transcription	Fetal Heart	heart
32	chr15:42104000-42117200	Strong transcription	Brain Angular Gyrus	brain
33	chr15:42104000-42118200	Strong transcription	Stomach Smooth Muscle	stomach
34	chr15:42104000-42118600	Strong transcription	NHLF	lung
35	chr15:42104000-42118800	Strong transcription	Cortex derived primary cultured neurospheres	brain
36	chr15:42104000-42119000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr15:42104000-42119000	Strong transcription	Fetal Muscle Leg	muscle
38	chr15:42104200-42110400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
39	chr15:42104200-42110800	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr15:42104200-42111400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr15:42104200-42111600	Strong transcription	NHDF-Ad	bronchial
42	chr15:42104200-42111800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
43	chr15:42104200-42113000	Strong transcription	Duodenum Mucosa	Duodenum
44	chr15:42104200-42113800	Strong transcription	Dnd41	blood
45	chr15:42104200-42117000	Strong transcription	Rectal Mucosa Donor 29	rectum
46	chr15:42104200-42117200	Strong transcription	Adipose Nuclei	Adipose
47	chr15:42104200-42117200	Strong transcription	Brain Cingulate Gyrus	brain
48	chr15:42104200-42117800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr15:42104200-42117800	Strong transcription	Fetal Thymus	thymus
50	chr15:42104200-42117800	Strong transcription	Ovary	ovary

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