Variant report

Variant	nsv1052910
Chromosome Location	chr15:78608637-78707049
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1098)
CpG islands
(count:2563)
Chromatin interactive
region (count:104)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1098 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:78609692-78610089	K562	blood:	n/a	n/a
2	ATF1	chr15:78667431-78667703	K562	blood:	n/a	n/a
3	ATF2	chr15:78614660-78615125	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr15:78687493-78688091	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr15:78617012-78617411	GM12878	blood:	n/a	n/a
6	ATF3	chr15:78643677-78643920	K562	blood:	n/a	n/a
7	BACH1	chr15:78617591-78617693	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr15:78633433-78633767	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr15:78608906-78609023	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr15:78632920-78633180	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr15:78679664-78679757	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr15:78660554-78660608	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr15:78696514-78696751	GM12878	blood:	n/a	n/a
14	BCL3	chr15:78617026-78617444	GM12878	blood:	n/a	n/a
15	BHLHE40	chr15:78645499-78645826	K562	blood:	n/a	n/a
16	BHLHE40	chr15:78667034-78667577	HepG2	liver:	n/a	n/a
17	BHLHE40	chr15:78615483-78615880	K562	blood:	n/a	n/a
18	BHLHE40	chr15:78661065-78661331	K562	blood:	n/a	n/a
19	BHLHE40	chr15:78609629-78609994	K562	blood:	n/a	n/a
20	BHLHE40	chr15:78667175-78667403	K562	blood:	n/a	n/a
21	BRCA1	chr15:78609738-78610092	Hela-S3	cervix:	n/a	n/a
22	BRCA1	chr15:78609821-78610091	H1-hESC	embryonic stem cell:	n/a	n/a
23	BRCA1	chr15:78633049-78633341	H1-hESC	embryonic stem cell:	n/a	n/a
24	BRCA1	chr15:78667535-78667586	Hela-S3	cervix:	n/a	n/a
25	CBX3	chr15:78645371-78645776	K562	blood:	n/a	n/a
26	CBX3	chr15:78645414-78645791	K562	blood:	n/a	n/a
27	CEBPB	chr15:78691461-78691950	A549	lung:	n/a	chr15:78691572-78691583 chr15:78691911-78691924
28	CEBPB	chr15:78644377-78644539	K562	blood:	n/a	chr15:78644422-78644433
29	CEBPB	chr15:78691523-78691917	K562	blood:	n/a	chr15:78691572-78691583
30	CEBPB	chr15:78667483-78667752	HepG2	liver:	n/a	n/a
31	CEBPB	chr15:78679906-78680059	HepG2	liver:	n/a	chr15:78679969-78679980
32	CEBPB	chr15:78619909-78620155	A549	lung:	n/a	chr15:78620001-78620012
33	CEBPB	chr15:78653596-78653796	K562	blood:	n/a	chr15:78653675-78653686
34	CEBPB	chr15:78614738-78615007	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr15:78619831-78620183	Hela-S3	cervix:	n/a	chr15:78620001-78620012
36	CEBPB	chr15:78679943-78680029	K562	blood:	n/a	chr15:78679969-78679980
37	CEBPB	chr15:78699678-78699833	IMR90	lung:	n/a	n/a
38	CEBPB	chr15:78684894-78685010	H1-hESC	embryonic stem cell:	n/a	chr15:78684947-78684955
39	CEBPB	chr15:78619858-78620186	HepG2	liver:	n/a	chr15:78620001-78620012
40	CEBPB	chr15:78667442-78667814	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr15:78697885-78698153	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr15:78644358-78644552	HepG2	liver:	n/a	chr15:78644422-78644433
43	CEBPB	chr15:78689340-78689684	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr15:78689360-78689698	HepG2	liver:	n/a	n/a
45	CEBPB	chr15:78699666-78699856	K562	blood:	n/a	n/a
46	CEBPB	chr15:78691450-78691710	HepG2	liver:	n/a	chr15:78691572-78691583
47	CEBPB	chr15:78687011-78687141	A549	lung:	n/a	n/a
48	CEBPB	chr15:78703386-78704085	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr15:78689530-78689561	IMR90	lung:	n/a	n/a
50	CEBPB	chr15:78644263-78644569	A549	lung:	n/a	chr15:78644422-78644433

(count:2563 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:78632579-78632629	BJ	skin:	n/a
2	chr15:78632579-78632629	BJ	skin:	n/a
3	chr15:78632184-78632234	K562	blood:	n/a
4	chr15:78623765-78623815	SK-N-SH_RA	brain:	n/a
5	chr15:78632677-78632727	NT2-D1	testis:	n/a
6	chr15:78633455-78633505	HCPEpiC	choroid plexus:	n/a
7	chr15:78632144-78632194	HNPCEpiC	eye:	n/a
8	chr15:78632081-78632131	NB4	blood:	n/a
9	chr15:78640536-78640586	HRE	kidney:	n/a
10	chr15:78631963-78632013	A549	lung:	n/a
11	chr15:78679693-78679743	AoSMC	blood vessel:	n/a
12	chr15:78632144-78632194	ovcar-3	ovarian:	n/a
13	chr15:78651749-78651799	HRPEpiC	eye:	n/a
14	chr15:78634235-78634285	NHDF-neo	bronchial:	n/a
15	chr15:78632144-78632194	Hela-S3	cervix:	n/a
16	chr15:78633455-78633505	Hela-S3	cervix:	n/a
17	chr15:78632859-78632909	HCT-116	colon:	n/a
18	chr15:78632592-78632642	HNPCEpiC	eye:	n/a
19	chr15:78631626-78631676	Caco-2	colon:	n/a
20	chr15:78632184-78632234	HUVEC	blood vessel:	n/a
21	chr15:78632859-78632909	BE2_C	brain:	n/a
22	chr15:78697933-78697983	HNPCEpiC	eye:	n/a
23	chr15:78632684-78632734	HNPCEpiC	eye:	n/a
24	chr15:78631179-78631229	A549	lung:	n/a
25	chr15:78631626-78631676	HCF	heart:	n/a
26	chr15:78614908-78614958	GM12892	blood:	n/a
27	chr15:78632194-78632244	ProgFib	skin:	n/a
28	chr15:78634235-78634285	AG04449	skin:	fetal
29	chr15:78632144-78632194	SAEC	small airway:	n/a
30	chr15:78632194-78632244	SK-N-MC	brain:	n/a
31	chr15:78631878-78631928	HepG2	liver:	n/a
32	chr15:78633437-78633487	HPAEpiC	pulmonary alveolar:	n/a
33	chr15:78697933-78697983	ECC-1	luminal epithelium:	n/a
34	chr15:78633202-78633252	GM12878	blood:	n/a
35	chr15:78697933-78697983	GM12878	blood:	n/a
36	chr15:78632592-78632642	Hela-S3	cervix:	n/a
37	chr15:78632670-78632720	SK-N-SH_RA	brain:	n/a
38	chr15:78633437-78633487	HRPEpiC	eye:	n/a
39	chr15:78637901-78637951	SK-N-SH_RA	brain:	n/a
40	chr15:78640434-78640484	AG04449	skin:	fetal
41	chr15:78632677-78632727	HepG2	liver:	n/a
42	chr15:78632194-78632244	HCF	heart:	n/a
43	chr15:78632670-78632720	NHBE	bronchial:	n/a
44	chr15:78637901-78637951	HepG2	liver:	n/a
45	chr15:78631196-78631246	ECC-1	luminal epithelium:	n/a
46	chr15:78632861-78632911	ECC-1	luminal epithelium:	n/a
47	chr15:78632144-78632194	Jurkat	blood:	n/a
48	chr15:78632677-78632727	A549	lung:	n/a
49	chr15:78632109-78632159	AG10803	skin:	n/a
50	chr15:78632861-78632911	NHDF-neo	bronchial:	n/a

(count:104 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr15:78691109..78692723-chr15:78696041..78697844,2	K562	blood:
2	chr15:78615016..78616729-chr15:78621265..78622957,2	K562	blood:
3	chr15:78600701..78601454-chr15:78609714..78610487,3	MCF-7	breast:
4	chr15:78630619..78632964-chr15:78634771..78637227,2	K562	blood:
5	chr15:78633360..78636306-chr15:78640174..78642916,2	MCF-7	breast:
6	chr15:78609337..78610241-chr15:78707562..78708403,2	MCF-7	breast:
7	chr15:78660412..78663253-chr15:78666199..78668825,4	MCF-7	breast:
8	chr15:78688849..78689413-chr15:78707506..78708008,2	MCF-7	breast:
9	chr15:78608718..78610938-chr15:78740404..78742745,2	K562	blood:
10	chr15:78658425..78660009-chr15:78663062..78665725,3	K562	blood:
11	chr15:78658425..78659935-chr15:78663062..78665442,2	K562	blood:
12	chr15:78658425..78660009-chr15:78663062..78665725,3	K562	blood:
13	chr15:78654127..78657076-chr15:78665731..78668813,3	MCF-7	breast:
14	chr15:78627367..78629049-chr15:78633476..78635413,2	K562	blood:
15	chr15:78689276..78690993-chr15:78695129..78697565,2	K562	blood:
16	chr15:78602775..78604649-chr15:78608220..78609992,2	K562	blood:
17	chr15:78622789..78627489-chr15:78629672..78633928,5	MCF-7	breast:
18	chr15:78689388..78691661-chr15:78857643..78859305,2	MCF-7	breast:
19	chr15:78640272..78641260-chr15:78688964..78689871,3	MCF-7	breast:
20	chr15:78653965..78657073-chr15:78658751..78661032,3	K562	blood:
21	chr15:78686256..78688855-chr15:78690068..78692853,2	K562	blood:
22	chr15:78607811..78611312-chr15:78615142..78617674,3	K562	blood:
23	chr15:78630690..78632557-chr15:78664334..78666586,2	K562	blood:
24	chr15:78618188..78620654-chr15:78728966..78731813,2	MCF-7	breast:
25	chr15:78607811..78609388-chr15:78615154..78616830,2	K562	blood:
26	chr15:78679630..78681837-chr15:78689698..78692156,2	MCF-7	breast:
27	chr15:78665803..78668679-chr15:78697732..78701698,4	MCF-7	breast:
28	chr15:78688934..78689473-chr15:78707850..78708354,2	MCF-7	breast:
29	chr15:78658425..78659935-chr15:78663062..78665442,2	K562	blood:
30	chr15:78615567..78617904-chr15:78638548..78641463,2	K562	blood:
31	chr15:78651423..78654019-chr15:78662111..78664837,3	MCF-7	breast:
32	chr15:78689276..78690993-chr15:78695129..78697565,2	K562	blood:
33	chr15:78607735..78608662-chr15:78707599..78708404,4	MCF-7	breast:
34	chr15:78648736..78650710-chr15:78656313..78658766,2	MCF-7	breast:
35	chr15:78657024..78658991-chr15:78692775..78694718,2	K562	blood:
36	chr15:78647379..78649715-chr15:78651896..78653984,2	K562	blood:
37	chr15:78609276..78610228-chr15:78689311..78689907,2	MCF-7	breast:
38	chr15:78679630..78681837-chr15:78689698..78692156,2	MCF-7	breast:
39	chr15:78638585..78642502-chr15:78665475..78668779,6	MCF-7	breast:
40	chr15:78627296..78629815-chr15:78701487..78704015,2	MCF-7	breast:
41	chr15:78666915..78668616-chr15:78678598..78681421,2	MCF-7	breast:
42	chr15:78591913..78593523-chr15:78605682..78608676,2	K562	blood:
43	chr15:78603756..78606983-chr15:78614948..78617752,3	K562	blood:
44	chr15:78660412..78663253-chr15:78666199..78668825,4	MCF-7	breast:
45	chr15:78633360..78636306-chr15:78640174..78642916,2	MCF-7	breast:
46	chr15:78609276..78610228-chr15:78689311..78689907,2	MCF-7	breast:
47	chr15:78631534..78633106-chr15:78696326..78697874,2	MCF-7	breast:
48	chr15:78607811..78611312-chr15:78615142..78617674,3	K562	blood:
49	chr15:78614726..78616366-chr15:78729558..78731110,2	MCF-7	breast:
50	chr15:78666064..78667576-chr15:78729924..78731852,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000259413	TF binding region
CRABP1	TF binding region
ENSG00000259413	CpG island
CRABP1	CpG island
ENSG00000140395	chromatin interactions
ENSG00000166426	chromatin interactions
ENSG00000169684	chromatin interactions
ENSG00000136381	chromatin interactions

Extended variants
information (count: 3807 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:3807 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561793201	chr15:78608657-78608658	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs576009670	chr15:78608701-78608702	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs544869348	chr15:78608704-78608705	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs550497996	chr15:78608705-78608706	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs569060109	chr15:78608726-78608727	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs533041841	chr15:78608756-78608757	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs116414034	chr15:78608764-78608765	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs566597130	chr15:78608775-78608776	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs533725953	chr15:78608832-78608833	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs555414349	chr15:78608858-78608859	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs568652058	chr15:78608873-78608874	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs151180621	chr15:78608893-78608894	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs189115251	chr15:78608924-78608925	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs575829247	chr15:78608933-78608934	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs546002638	chr15:78608964-78608965	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs557783886	chr15:78608967-78608968	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs182503286	chr15:78608982-78608983	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs540222967	chr15:78608991-78608992	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs562157832	chr15:78608993-78608994	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs186252339	chr15:78609006-78609007	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs77546254	chr15:78609016-78609017	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs190665552	chr15:78609028-78609029	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs372021179	chr15:78609034-78609035	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs578141451	chr15:78609076-78609077	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs540749120	chr15:78609077-78609078	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs551607726	chr15:78609108-78609109	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs140288367	chr15:78609144-78609145	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs182750719	chr15:78609170-78609171	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs542489403	chr15:78609171-78609172	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs560271077	chr15:78609189-78609190	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs373309679	chr15:78609231-78609232	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs116196383	chr15:78609245-78609246	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs375202446	chr15:78609248-78609249	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs556103395	chr15:78609249-78609250	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs535758099	chr15:78609310-78609311	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs373461449	chr15:78609334-78609335	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs557599041	chr15:78609410-78609411	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs569452430	chr15:78609434-78609435	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs578212110	chr15:78609444-78609445	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs539603326	chr15:78609458-78609459	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs557968641	chr15:78609472-78609473	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs185490245	chr15:78609494-78609495	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs529253263	chr15:78609535-78609536	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs540353811	chr15:78609542-78609543	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs555459777	chr15:78609546-78609547	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs573941803	chr15:78609563-78609564	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs374794173	chr15:78609572-78609573	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs77850614	chr15:78609583-78609584	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs562758900	chr15:78609601-78609602	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs578007628	chr15:78609651-78609652	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Wilms tumour	21544195	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
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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	17322880	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Autism	21480499	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	16864856	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17133270	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16774939	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Sudden cardiac death	19188705	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	21364760	CNVD

Chromatin state (count:1541 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:78601400-78616800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr15:78602400-78609000	Weak transcription	Small Intestine	intestine
3	chr15:78607600-78610200	Enhancers	Fetal Stomach	stomach
4	chr15:78608000-78608800	Enhancers	Fetal Muscle Trunk	muscle
5	chr15:78608000-78609400	Enhancers	Rectal Mucosa Donor 31	rectum
6	chr15:78608000-78609600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr15:78608000-78609800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr15:78608000-78609800	Enhancers	Brain Anterior Caudate	brain
9	chr15:78608000-78609800	Enhancers	Brain Hippocampus Middle	brain
10	chr15:78608000-78609800	Enhancers	Brain Substantia Nigra	brain
11	chr15:78608000-78609800	Enhancers	Placenta Amnion	Placenta Amnion
12	chr15:78608000-78610000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr15:78608200-78608800	Enhancers	Hela-S3	cervix
14	chr15:78608200-78609000	Bivalent Enhancer	HepG2	liver
15	chr15:78608200-78609400	Enhancers	Duodenum Mucosa	Duodenum
16	chr15:78608200-78609400	Enhancers	Rectal Mucosa Donor 29	rectum
17	chr15:78608200-78609600	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr15:78608200-78609800	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr15:78608200-78609800	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr15:78608200-78609800	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr15:78608200-78609800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr15:78608200-78609800	Enhancers	Brain Cingulate Gyrus	brain
23	chr15:78608200-78609800	Enhancers	Colonic Mucosa	Colon
24	chr15:78608200-78610000	Enhancers	H1 Cell Line	embryonic stem cell
25	chr15:78608200-78610000	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr15:78608200-78610000	Enhancers	Fetal Intestine Large	intestine
27	chr15:78608200-78610000	Enhancers	Placenta	Placenta
28	chr15:78608200-78610000	Enhancers	Stomach Mucosa	stomach
29	chr15:78608200-78610200	Enhancers	Fetal Intestine Small	intestine
30	chr15:78608400-78609400	Enhancers	Cortex derived primary cultured neurospheres	brain
31	chr15:78608400-78609600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr15:78608400-78609600	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr15:78608400-78609600	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr15:78608400-78609600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr15:78608400-78609600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
36	chr15:78608400-78609800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr15:78608600-78608800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr15:78608600-78608800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr15:78608600-78608800	Enhancers	Gastric	stomach
40	chr15:78608600-78608800	Enhancers	Sigmoid Colon	Sigmoid Colon
41	chr15:78608600-78609000	Weak transcription	Brain Angular Gyrus	brain
42	chr15:78608600-78609000	Weak transcription	Brain Inferior Temporal Lobe	brain
43	chr15:78608600-78609400	Enhancers	GM12878-XiMat	blood
44	chr15:78608600-78609600	Enhancers	H9 Cell Line	embryonic stem cell
45	chr15:78608600-78609800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr15:78608600-78609800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr15:78608600-78609800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr15:78608600-78609800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr15:78608600-78609800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr15:78608600-78609800	Enhancers	Fetal Heart	heart

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