Variant report

Variant	nsv904244
Chromosome Location	chr15:55687969-55770911
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1458)
CpG islands
(count:1160)
Chromatin interactive
region (count:62)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1458 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:55699681-55700995	HepG2	liver:	n/a	chr15:55699936-55699952
2	ARID3A	chr15:55711482-55711586	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:55694987-55696143	K562	blood:	n/a	n/a
4	ARID3A	chr15:55695766-55696116	HepG2	liver:	n/a	n/a
5	ARID3A	chr15:55693945-55694278	K562	blood:	n/a	n/a
6	ARID3A	chr15:55688544-55689215	K562	blood:	n/a	n/a
7	ARID3A	chr15:55700139-55701084	K562	blood:	n/a	n/a
8	ATF1	chr15:55700302-55701186	K562	blood:	n/a	n/a
9	ATF1	chr15:55731955-55732174	K562	blood:	n/a	n/a
10	ATF1	chr15:55695695-55696130	K562	blood:	n/a	n/a
11	ATF2	chr15:55700143-55700984	GM12878	blood:	n/a	n/a
12	ATF2	chr15:55700234-55700505	GM12878	blood:	n/a	n/a
13	ATF2	chr15:55700338-55700728	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF3	chr15:55695638-55696206	K562	blood:	n/a	n/a
15	ATF3	chr15:55697469-55697665	K562	blood:	n/a	n/a
16	ATF3	chr15:55700118-55701112	A549	lung:	n/a	n/a
17	ATF3	chr15:55700358-55700740	K562	blood:	n/a	n/a
18	BACH1	chr15:55695752-55696274	K562	blood:	n/a	n/a
19	BACH1	chr15:55693951-55694258	K562	blood:	n/a	n/a
20	BACH1	chr15:55700665-55700854	K562	blood:	n/a	n/a
21	BACH1	chr15:55700619-55701045	H1-hESC	embryonic stem cell:	n/a	n/a
22	BCL3	chr15:55700313-55701096	A549	lung:	n/a	chr15:55700652-55700665 chr15:55700787-55700795 chr15:55700649-55700662
23	BCLAF1	chr15:55700180-55700876	GM12878	blood:	n/a	chr15:55700652-55700665 chr15:55700787-55700795 chr15:55700649-55700662
24	BCLAF1	chr15:55700112-55700929	GM12878	blood:	n/a	chr15:55700652-55700665 chr15:55700787-55700795 chr15:55700649-55700662
25	BHLHE40	chr15:55699728-55701170	K562	blood:	n/a	chr15:55700654-55700670 chr15:55700528-55700544 chr15:55700677-55700693
26	BHLHE40	chr15:55690413-55690747	K562	blood:	n/a	chr15:55690612-55690625
27	BHLHE40	chr15:55697522-55697947	K562	blood:	n/a	n/a
28	BHLHE40	chr15:55689050-55689682	K562	blood:	n/a	n/a
29	BHLHE40	chr15:55731973-55732178	GM12878	blood:	n/a	n/a
30	BHLHE40	chr15:55694074-55694195	K562	blood:	n/a	n/a
31	BHLHE40	chr15:55700025-55701233	GM12878	blood:	n/a	chr15:55700654-55700670 chr15:55700528-55700544 chr15:55700677-55700693
32	BRCA1	chr15:55700452-55700784	HepG2	liver:	n/a	n/a
33	BRCA1	chr15:55700467-55700697	GM12878	blood:	n/a	n/a
34	BRCA1	chr15:55699596-55701223	Hela-S3	cervix:	n/a	n/a
35	BRCA1	chr15:55700512-55700973	H1-hESC	embryonic stem cell:	n/a	n/a
36	CBX3	chr15:55700369-55700677	K562	blood:	n/a	n/a
37	CBX3	chr15:55697420-55697995	K562	blood:	n/a	n/a
38	CBX3	chr15:55700143-55700934	K562	blood:	n/a	n/a
39	CCNT2	chr15:55695657-55696054	K562	blood:	n/a	n/a
40	CCNT2	chr15:55689104-55689478	K562	blood:	n/a	n/a
41	CCNT2	chr15:55699564-55700830	K562	blood:	n/a	n/a
42	CEBPB	chr15:55695675-55696056	IMR90	lung:	n/a	chr15:55695839-55695856 chr15:55695841-55695852
43	CEBPB	chr15:55712757-55712999	A549	lung:	n/a	chr15:55712901-55712912
44	CEBPB	chr15:55695654-55696207	K562	blood:	n/a	chr15:55695839-55695856 chr15:55695841-55695852
45	CEBPB	chr15:55694933-55696193	Hela-S3	cervix:	n/a	chr15:55695839-55695856 chr15:55695841-55695852
46	CEBPB	chr15:55695703-55695997	K562	blood:	n/a	chr15:55695839-55695856 chr15:55695841-55695852
47	CEBPB	chr15:55701450-55701624	HepG2	liver:	n/a	chr15:55701553-55701564
48	CEBPB	chr15:55695663-55696047	HepG2	liver:	n/a	chr15:55695839-55695856 chr15:55695841-55695852
49	CEBPB	chr15:55695666-55696177	HCT-116	colon:	n/a	chr15:55695839-55695856 chr15:55695841-55695852
50	CEBPB	chr15:55762701-55762873	IMR90	lung:	n/a	chr15:55762795-55762806

(count:1160 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:55700482-55700532	HNPCEpiC	eye:	n/a
2	chr15:55700482-55700532	HNPCEpiC	eye:	n/a
3	chr15:55700587-55700637	NHBE	bronchial:	n/a
4	chr15:55701181-55701231	Hela-S3	cervix:	n/a
5	chr15:55700901-55700951	NB4	blood:	n/a
6	chr15:55700718-55700768	GM19239	blood:	n/a
7	chr15:55700718-55700768	HL-60	blood:	n/a
8	chr15:55700593-55700643	HNPCEpiC	eye:	n/a
9	chr15:55700780-55700830	BE2_C	brain:	n/a
10	chr15:55697065-55697115	HMEC	breast:	n/a
11	chr15:55700689-55700739	AG10803	skin:	n/a
12	chr15:55700768-55700818	A549	lung:	n/a
13	chr15:55701181-55701231	HRE	kidney:	n/a
14	chr15:55737718-55737768	GM12892	blood:	n/a
15	chr15:55700718-55700768	U87	brain:	n/a
16	chr15:55700587-55700637	HRE	kidney:	n/a
17	chr15:55700593-55700643	HCT-116	colon:	n/a
18	chr15:55700768-55700818	T-47D	breast:	n/a
19	chr15:55700549-55700599	HCPEpiC	choroid plexus:	n/a
20	chr15:55700768-55700818	HNPCEpiC	eye:	n/a
21	chr15:55700549-55700599	H1-hESC	embryonic stem cell:	embryo
22	chr15:55700901-55700951	HAEpiC	amniotic membrane:	n/a
23	chr15:55700780-55700830	GM12892	blood:	n/a
24	chr15:55737718-55737768	HRCEpiC	kidney:	n/a
25	chr15:55701181-55701231	PrEC	prostate:	n/a
26	chr15:55700718-55700768	RPTEC	kidney:	n/a
27	chr15:55700780-55700830	GM06990	blood:	n/a
28	chr15:55700689-55700739	K562	blood:	n/a
29	chr15:55700768-55700818	PFSK-1	brain:	n/a
30	chr15:55704519-55704569	IMR90	lung:	fetal
31	chr15:55700482-55700532	H1-hESC	embryonic stem cell:	embryo
32	chr15:55700549-55700599	HL-60	blood:	n/a
33	chr15:55700743-55700793	GM12878	blood:	n/a
34	chr15:55700901-55700951	ECC-1	luminal epithelium:	n/a
35	chr15:55700780-55700830	HCF	heart:	n/a
36	chr15:55700471-55700521	AoSMC	blood vessel:	n/a
37	chr15:55704519-55704569	RPTEC	kidney:	n/a
38	chr15:55700431-55700481	AG09309	skin:	n/a
39	chr15:55700718-55700768	CMK	blood:	n/a
40	chr15:55704519-55704569	Hela-S3	cervix:	n/a
41	chr15:55710020-55710070	BJ	skin:	n/a
42	chr15:55737718-55737768	SAEC	small airway:	n/a
43	chr15:55701181-55701231	NHDF-neo	bronchial:	n/a
44	chr15:55704519-55704569	HRE	kidney:	n/a
45	chr15:55700482-55700532	CMK	blood:	n/a
46	chr15:55701181-55701231	RPTEC	kidney:	n/a
47	chr15:55704519-55704569	HEK293	kidney:	embryo
48	chr15:55700471-55700521	HCPEpiC	choroid plexus:	n/a
49	chr15:55700780-55700830	SAEC	small airway:	n/a
50	chr15:55700901-55700951	BE2_C	brain:	n/a

(count:62 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr15:55650827..55653650-chr15:55729879..55732717,2	K562	blood:
2	chr15:55609877..55611698-chr15:55698360..55701817,3	MCF-7	breast:
3	chr15:55687261..55690621-chr15:55699123..55703142,5	K562	blood:
4	chr15:55700055..55700776-chr6:35435724..35436851,3	Hela-S3	cervix:
5	chr15:55581601..55584571-chr15:55728734..55731543,2	K562	blood:
6	chr15:55509574..55510417-chr15:55731604..55732340,2	MCF-7	breast:
7	chr15:55699975..55700679-chr17:56735984..56736735,2	Hela-S3	cervix:
8	chr15:55697625..55700554-chr15:55706676..55709673,2	K562	blood:
9	chr15:55580643..55583951-chr15:55698978..55701737,3	K562	blood:
10	chr15:55631303..55633200-chr15:55699872..55702073,2	MCF-7	breast:
11	chr15:55701169..55703678-chr15:55710788..55712535,2	MCF-7	breast:
12	chr15:55608625..55613147-chr15:55698683..55702764,8	MCF-7	breast:
13	chr15:55701169..55703678-chr15:55710788..55712535,2	MCF-7	breast:
14	chr15:55486981..55489906-chr15:55690724..55692379,2	K562	blood:
15	chr15:55613382..55615549-chr15:55714258..55716081,2	K562	blood:
16	chr15:55700044..55700555-chr15:65596754..65597469,2	Hela-S3	cervix:
17	chr15:55689930..55691529-chr15:55699148..55701673,2	MCF-7	breast:
18	chr15:55698992..55701610-chr15:55725082..55727679,2	K562	blood:
19	chr15:55699965..55700846-chr15:65587988..65588628,2	Hela-S3	cervix:
20	chr15:55696852..55699665-chr15:55712534..55714960,2	K562	blood:
21	chr15:55582304..55584506-chr15:55726191..55728043,2	MCF-7	breast:
22	chr15:55686108..55691081-chr15:55692026..55698243,11	K562	blood:
23	chr13:29973836..29976815-chr15:55698261..55699841,2	K562	blood:
24	chr15:55700578..55702237-chr15:55707126..55709409,2	MCF-7	breast:
25	chr15:55694340..55696767-chr15:55697475..55699670,2	MCF-7	breast:
26	chr15:55610040..55612568-chr15:55696345..55698141,2	MCF-7	breast:
27	chr15:55699692..55700583-chr3:169482758..169483656,2	Hela-S3	cervix:
28	chr15:55509498..55510422-chr15:55731553..55732482,2	K562	blood:
29	chr15:55711236..55714133-chr15:55717728..55719591,2	K562	blood:
30	chr15:55696852..55699665-chr15:55712534..55714960,2	K562	blood:
31	chr15:55607682..55613892-chr15:55697623..55703247,7	K562	blood:
32	chr15:55711236..55714133-chr15:55717728..55719591,2	K562	blood:
33	chr15:55577567..55579089-chr15:55694528..55696394,2	K562	blood:
34	chr15:55582032..55583811-chr15:55727186..55728164,12	MCF-7	breast:
35	chr15:55698446..55701018-chr15:55709702..55712524,2	MCF-7	breast:
36	chr15:55610027..55612992-chr15:55688713..55692198,3	K562	blood:
37	chr15:55509736..55510399-chr15:55727358..55727891,2	MCF-7	breast:
38	chr15:55698446..55701018-chr15:55709702..55712524,2	MCF-7	breast:
39	chr15:55609981..55613646-chr15:55692667..55696745,4	K562	blood:
40	chr15:55486571..55488270-chr15:55698193..55700233,2	K562	blood:
41	chr12:92538794..92539703-chr15:55699924..55700498,2	Hela-S3	cervix:
42	chr13:60970048..60970785-chr15:55700070..55700954,2	Hela-S3	cervix:
43	chr15:55708123..55710711-chr15:55711539..55714446,2	K562	blood:
44	chr15:55579894..55582757-chr15:55689915..55691723,2	K562	blood:
45	chr15:55687039..55689361-chr15:55690418..55692819,3	K562	blood:
46	chr15:55607556..55615100-chr15:55699006..55703115,13	K562	blood:
47	chr15:55572408..55575581-chr15:55726220..55729674,3	K562	blood:
48	chr15:55609398..55612428-chr15:55693917..55698358,4	K562	blood:
49	chr15:55687284..55689317-chr15:55695984..55697982,2	MCF-7	breast:
50	chr15:55656332..55658633-chr15:55699668..55701557,2	MCF-7	breast:

No data

Variant related genes	Relation type
C15orf65	TF binding region
CCPG1	TF binding region
ENSG00000260036	TF binding region
C15orf65	CpG island
CCPG1	CpG island
ENSG00000260036	CpG island
ENSG00000198755	chromatin interactions
ENSG00000137876	chromatin interactions
ENSG00000083544	chromatin interactions
ENSG00000270141	chromatin interactions
ENSG00000133639	chromatin interactions
ENSG00000069974	chromatin interactions
ENSG00000260916	chromatin interactions
ENSG00000245904	chromatin interactions
ENSG00000199568	chromatin interactions
ENSG00000107164	chromatin interactions
ENSG00000261652	chromatin interactions
ENSG00000225973	chromatin interactions
ENSG00000069943	chromatin interactions
ENSG00000202077	chromatin interactions
ENSG00000072042	chromatin interactions
ENSG00000200156	chromatin interactions

Extended variants
information (count: 3672 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:3672 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7170993	chr15:55687969-55687970	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs560913239	chr15:55687971-55687972	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs541873170	chr15:55688135-55688136	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs149047324	chr15:55688169-55688170	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs549458968	chr15:55688196-55688197	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs578054339	chr15:55688246-55688247	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs143073222	chr15:55688253-55688254	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs551707815	chr15:55688257-55688258	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs565691027	chr15:55688306-55688307	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs147809636	chr15:55688335-55688336	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs555277105	chr15:55688346-55688347	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs57419686	chr15:55688353-55688354	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs572355531	chr15:55688354-55688355	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs568538705	chr15:55688364-55688365	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs398027376	chr15:55688369-55688370	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs180979430	chr15:55688424-55688425	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs557597770	chr15:55688471-55688472	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs577365644	chr15:55688481-55688482	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs546343598	chr15:55688510-55688511	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs553060264	chr15:55688524-55688525	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs201242803	chr15:55688534-55688535	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs374260468	chr15:55688539-55688540	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs573225964	chr15:55688547-55688548	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs540948275	chr15:55688605-55688606	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs561286283	chr15:55688748-55688749	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs200485903	chr15:55688766-55688767	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs144531102	chr15:55688767-55688768	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs529826854	chr15:55688913-55688914	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs543170941	chr15:55688953-55688954	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs563143849	chr15:55688957-55688958	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs532051325	chr15:55688969-55688970	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs552266262	chr15:55689045-55689046	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs34372408	chr15:55689077-55689078	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs528117464	chr15:55689086-55689087	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs146992016	chr15:55689092-55689093	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs73406933	chr15:55689097-55689098	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs537742352	chr15:55689128-55689129	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs372774151	chr15:55689144-55689145	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs557560555	chr15:55689155-55689156	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs571070509	chr15:55689165-55689166	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs185458695	chr15:55689221-55689222	Weak transcription Enhancers Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs371048465	chr15:55689225-55689226	Weak transcription Enhancers Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs199503799	chr15:55689234-55689235	Weak transcription Enhancers Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs575651653	chr15:55689255-55689256	Weak transcription Enhancers Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs190813562	chr15:55689257-55689258	Weak transcription Enhancers Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs573149371	chr15:55689269-55689270	Weak transcription Enhancers Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs386784234	chr15:55689278-55689279	Weak transcription Enhancers Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs113777098	chr15:55689279-55689280	Weak transcription Enhancers Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs4774210	chr15:55689280-55689281	Weak transcription Enhancers Active TSS	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs574347203	chr15:55689309-55689310	Weak transcription Enhancers Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	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
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	22032731	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Cancer	21129771	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Myelofibrosis	22110671	CNVD
Acute monocytic leukemia	16498392	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:811 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:55611800-55699400	Weak transcription	Colonic Mucosa	Colon
2	chr15:55630000-55695000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
3	chr15:55637000-55699600	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr15:55647800-55695400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
5	chr15:55649800-55695800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
6	chr15:55668200-55699800	Weak transcription	Spleen	Spleen
7	chr15:55669400-55690400	Weak transcription	Fetal Heart	heart
8	chr15:55670200-55695000	Weak transcription	Colon Smooth Muscle	Colon
9	chr15:55671800-55690400	Weak transcription	Brain Angular Gyrus	brain
10	chr15:55671800-55695800	Weak transcription	HSMMtube	muscle
11	chr15:55672200-55696000	Weak transcription	Brain Substantia Nigra	brain
12	chr15:55676000-55695000	Weak transcription	Pancreatic Islets	Pancreatic Islet
13	chr15:55676000-55699400	Weak transcription	Brain Cingulate Gyrus	brain
14	chr15:55676200-55695200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr15:55676200-55695800	Weak transcription	Brain Hippocampus Middle	brain
16	chr15:55676400-55697200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr15:55676400-55699400	Weak transcription	Right Ventricle	heart
18	chr15:55676800-55688600	Weak transcription	Aorta	Aorta
19	chr15:55676800-55695800	Weak transcription	Rectal Mucosa Donor 31	rectum
20	chr15:55676800-55697600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
21	chr15:55677000-55695600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
22	chr15:55678200-55699400	Weak transcription	Brain Inferior Temporal Lobe	brain
23	chr15:55679400-55696800	Weak transcription	Primary T cells fromperipheralblood	blood
24	chr15:55679600-55689600	Weak transcription	Rectal Mucosa Donor 29	rectum
25	chr15:55679600-55694400	Weak transcription	Sigmoid Colon	Sigmoid Colon
26	chr15:55679600-55695000	Weak transcription	Fetal Intestine Large	intestine
27	chr15:55681000-55688600	Weak transcription	Adipose Nuclei	Adipose
28	chr15:55681000-55695000	Weak transcription	Primary B cells from peripheral blood	blood
29	chr15:55681000-55695800	Weak transcription	Rectal Smooth Muscle	rectum
30	chr15:55681000-55697400	Weak transcription	Gastric	stomach
31	chr15:55681000-55699200	Weak transcription	Lung	lung
32	chr15:55681000-55699600	Weak transcription	Fetal Stomach	stomach
33	chr15:55681200-55689800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
34	chr15:55681200-55693800	Weak transcription	Primary T helper cells fromperipheralblood	blood
35	chr15:55681200-55694000	Weak transcription	Liver	Liver
36	chr15:55681200-55694200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr15:55681200-55694400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
38	chr15:55681200-55695000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
39	chr15:55681200-55695600	Weak transcription	Fetal Intestine Small	intestine
40	chr15:55681200-55699400	Weak transcription	Stomach Smooth Muscle	stomach
41	chr15:55681400-55695800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
42	chr15:55681600-55695600	Weak transcription	Primary T helper cells PMA-I stimulated	--
43	chr15:55681800-55688200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr15:55681800-55695200	Weak transcription	Stomach Mucosa	stomach
45	chr15:55681800-55699600	Weak transcription	NHLF	lung
46	chr15:55682000-55688400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr15:55682000-55688400	Weak transcription	Muscle Satellite Cultured Cells	--
48	chr15:55682600-55695200	Weak transcription	Primary T cells from cord blood	blood
49	chr15:55685400-55688000	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
50	chr15:55685400-55689000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood

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