Variant report

Variant	nsv569602
Chromosome Location	chr15:58914326-58964437
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	chr15:58961444-58961957	K562	blood:	n/a	chr15:58961720-58961736
2	ARID3A	chr15:58918774-58919007	HepG2	liver:	n/a	n/a
3	ATF1	chr15:58961450-58961769	K562	blood:	n/a	n/a
4	CBX3	chr15:58949525-58949776	K562	blood:	n/a	n/a
5	CCNT2	chr15:58961404-58961791	K562	blood:	n/a	chr15:58961565-58961585
6	CCNT2	chr15:58919885-58919962	K562	blood:	n/a	n/a
7	CEBPB	chr15:58918503-58918845	HepG2	liver:	n/a	n/a
8	CEBPB	chr15:58936462-58936497	IMR90	lung:	n/a	n/a
9	CEBPD	chr15:58961329-58961797	K562	blood:	n/a	n/a
10	CTCF	chr15:58958460-58958610	HRE	kidney:	n/a	n/a
11	CTCF	chr15:58947706-58947717	GM13976	blood:	n/a	n/a
12	CTCF	chr15:58949900-58950050	HEEpiC	esophagus:	n/a	n/a
13	CTCF	chr15:58947719-58947739	GM13976	blood:	n/a	n/a
14	CTCF	chr15:58946692-58946716	A549	lung:	n/a	n/a
15	CTCF	chr15:58922017-58922120	Fibrobl	skin:	n/a	n/a
16	CTCF	chr15:58916726-58916793	Spleen_OC	spleen:	n/a	n/a
17	CUX1	chr15:58941704-58941788	K562	blood:	n/a	n/a
18	CUX1	chr15:58961361-58961731	K562	blood:	n/a	n/a
19	CUX1	chr15:58940959-58940987	K562	blood:	n/a	n/a
20	E2F4	chr15:58948799-58949098	MCF10A-Er-Src	breast:	n/a	n/a
21	E2F4	chr15:58919657-58919857	MCF10A-Er-Src	breast:	n/a	n/a
22	EBF1	chr15:58918044-58918105	GM12878	blood:	n/a	chr15:58918062-58918073
23	EP300	chr15:58918645-58918820	HepG2	liver:	n/a	n/a
24	EP300	chr15:58961376-58961768	K562	blood:	n/a	n/a
25	EP300	chr15:58918535-58918961	HepG2	liver:	n/a	n/a
26	EP300	chr15:58918509-58918834	HepG2	liver:	n/a	n/a
27	FOS	chr15:58959172-58959530	MCF10A-Er-Src	breast:	n/a	chr15:58959343-58959353 chr15:58959344-58959352 chr15:58959340-58959351 chr15:58959345-58959352
28	FOS	chr15:58957968-58958129	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr15:58959175-58959509	MCF10A-Er-Src	breast:	n/a	chr15:58959343-58959353 chr15:58959344-58959352 chr15:58959340-58959351 chr15:58959345-58959352
30	FOS	chr15:58959163-58959498	MCF10A-Er-Src	breast:	n/a	chr15:58959343-58959353 chr15:58959344-58959352 chr15:58959340-58959351 chr15:58959345-58959352
31	FOS	chr15:58959172-58959509	MCF10A-Er-Src	breast:	n/a	chr15:58959343-58959353 chr15:58959344-58959352 chr15:58959340-58959351 chr15:58959345-58959352
32	FOSL2	chr15:58959039-58959640	A549	lung:	n/a	chr15:58959343-58959353 chr15:58959344-58959352 chr15:58959340-58959351 chr15:58959345-58959352
33	FOXA1	chr15:58924661-58924819	A549	lung:	n/a	n/a
34	FOXA1	chr15:58918475-58918944	HepG2	liver:	n/a	n/a
35	FOXA1	chr15:58918494-58918945	HepG2	liver:	n/a	n/a
36	FOXA2	chr15:58918543-58918852	HepG2	liver:	n/a	n/a
37	GATA2	chr15:58961344-58961803	K562	blood:	n/a	chr15:58961575-58961583
38	GATA3	chr15:58955152-58955304	SH-SY5Y	brain:	n/a	n/a
39	GATA3	chr15:58931570-58931770	SH-SY5Y	brain:	n/a	n/a
40	GATA3	chr15:58924057-58924257	SH-SY5Y	brain:	n/a	n/a
41	HDAC2	chr15:58918568-58918893	HepG2	liver:	n/a	n/a
42	IRF1	chr15:58920913-58921212	K562	blood:	n/a	chr15:58921057-58921071 chr15:58921056-58921067 chr15:58921051-58921068 chr15:58921057-58921067 chr15:58921055-58921075 chr15:58921056-58921070 chr15:58921056-58921069 chr15:58921053-58921067 chr15:58921059-58921073 chr15:58921051-58921072 chr15:58921056-58921069 chr15:58921054-58921068 chr15:58921056-58921069 chr15:58921055-58921066
43	IRF1	chr15:58942388-58942683	K562	blood:	n/a	n/a
44	IRF1	chr15:58961477-58962011	K562	blood:	n/a	n/a
45	IRF1	chr15:58920874-58921287	K562	blood:	n/a	chr15:58921057-58921071 chr15:58921056-58921067 chr15:58921051-58921068 chr15:58921057-58921067 chr15:58921055-58921075 chr15:58921056-58921070 chr15:58921056-58921069 chr15:58921053-58921067 chr15:58921059-58921073 chr15:58921051-58921072 chr15:58921056-58921069 chr15:58921054-58921068 chr15:58921056-58921069 chr15:58921055-58921066
46	IRF1	chr15:58928976-58929019	K562	blood:	n/a	n/a
47	IRF1	chr15:58942433-58942586	K562	blood:	n/a	n/a
48	IRF1	chr15:58920538-58921602	K562	blood:	n/a	chr15:58921057-58921071 chr15:58921056-58921067 chr15:58921051-58921068 chr15:58921057-58921067 chr15:58921055-58921075 chr15:58921056-58921070 chr15:58921056-58921069 chr15:58921053-58921067 chr15:58921059-58921073 chr15:58921051-58921072 chr15:58921056-58921069 chr15:58921054-58921068 chr15:58921056-58921069 chr15:58921055-58921066
49	JUN	chr15:58959169-58959450	HUVEC	blood vessel:	n/a	chr15:58959343-58959353 chr15:58959344-58959352 chr15:58959340-58959351 chr15:58959345-58959352
50	JUN	chr15:58957913-58958232	HepG2	liver:	n/a	chr15:58958068-58958081

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:58960059-58960109	HIPEpiC	eye:	n/a
2	chr15:58960059-58960109	Hela-S3	cervix:	n/a
3	chr15:58960059-58960109	HUVEC	blood vessel:	n/a
4	chr15:58960059-58960109	CMK	blood:	n/a
5	chr15:58960059-58960109	K562	blood:	n/a
6	chr15:58960059-58960109	HRCEpiC	kidney:	n/a
7	chr15:58960059-58960109	NT2-D1	testis:	n/a
8	chr15:58960059-58960109	A549	lung:	n/a
9	chr15:58960059-58960109	HCT-116	colon:	n/a
10	chr15:58960059-58960109	HRPEpiC	eye:	n/a
11	chr15:58960059-58960109	SAEC	small airway:	n/a
12	chr15:58960059-58960109	BJ	skin:	n/a
13	chr15:58960059-58960109	AG10803	skin:	n/a
14	chr15:58960059-58960109	HNPCEpiC	eye:	n/a
15	chr15:58960059-58960109	RPTEC	kidney:	n/a
16	chr15:58960059-58960109	GM12892	blood:	n/a
17	chr15:58960059-58960109	NH-A	brain:	n/a
18	chr15:58960059-58960109	GM12891	blood:	n/a
19	chr15:58960059-58960109	HEEpiC	esophagus:	n/a
20	chr15:58960059-58960109	HL-60	blood:	n/a
21	chr15:58960059-58960109	ovcar-3	ovarian:	n/a
22	chr15:58960059-58960109	ProgFib	skin:	n/a
23	chr15:58960059-58960109	IMR90	lung:	fetal
24	chr15:58960059-58960109	HMEC	breast:	n/a
25	chr15:58960059-58960109	H1-hESC	embryonic stem cell:	embryo
26	chr15:58960059-58960109	AG09319	gingival:	n/a
27	chr15:58960059-58960109	MCF-7	breast:	n/a
28	chr15:58960059-58960109	PANC-1	pancreas:	n/a
29	chr15:58960059-58960109	PrEC	prostate:	n/a
30	chr15:58960059-58960109	SK-N-SH	brain:	n/a
31	chr15:58960059-58960109	NHBE	bronchial:	n/a
32	chr15:58960059-58960109	SKMC	muscle:	n/a
33	chr15:58960059-58960109	AoSMC	blood vessel:	n/a
34	chr15:58960059-58960109	SK-N-MC	brain:	n/a
35	chr15:58960059-58960109	HepG2	liver:	n/a
36	chr15:58960059-58960109	HRE	kidney:	n/a
37	chr15:58960059-58960109	HPAEpiC	pulmonary alveolar:	n/a
38	chr15:58960059-58960109	HCPEpiC	choroid plexus:	n/a
39	chr15:58960059-58960109	T-47D	breast:	n/a
40	chr15:58960059-58960109	ECC-1	luminal epithelium:	n/a
41	chr15:58960059-58960109	PFSK-1	brain:	n/a
42	chr15:58960059-58960109	GM06990	blood:	n/a
43	chr15:58960059-58960109	MCF10A-Er-Src	breast:	n/a
44	chr15:58960059-58960109	AG04449	skin:	fetal
45	chr15:58960059-58960109	Jurkat	blood:	n/a
46	chr15:58960059-58960109	LNCaP	prostate:	n/a
47	chr15:58960059-58960109	GM12878	blood:	n/a
48	chr15:58960059-58960109	HCM	heart:	n/a
49	chr15:58960059-58960109	Hepatocyte	liver:	n/a
50	chr15:58960059-58960109	SK-N-SH_RA	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr15:58909393..58911330-chr15:58917319..58918979,2	K562	blood:
2	chr15:58953177..58955880-chr15:58958454..58961862,3	K562	blood:
3	chr15:58945480..58947689-chr15:59040936..59043629,2	K562	blood:
4	chr15:58915714..58920888-chr15:58922126..58927407,8	K562	blood:
5	chr15:58919702..58922554-chr15:58940056..58942110,2	K562	blood:
6	chr15:58957306..58961861-chr15:58967060..58970416,4	K562	blood:
7	chr15:58941689..58944037-chr15:58949556..58952654,3	K562	blood:
8	chr15:58927036..58929525-chr15:58931244..58932793,2	K562	blood:
9	chr15:58927036..58929525-chr15:58931244..58932793,2	K562	blood:
10	chr15:58949134..58952311-chr15:58956735..58961509,4	K562	blood:
11	chr15:58919916..58921624-chr15:58929696..58932530,2	K562	blood:
12	chr15:58919916..58921624-chr15:58929696..58932530,2	K562	blood:
13	chr15:58903672..58906413-chr15:58914641..58916719,2	K562	blood:
14	chr15:58939363..58941206-chr15:59062666..59064194,2	MCF-7	breast:
15	chr15:58938038..58940430-chr15:58949050..58951838,2	K562	blood:
16	chr15:58932722..58935543-chr15:58957168..58958694,2	K562	blood:
17	chr15:58949134..58952311-chr15:58956735..58961509,4	K562	blood:
18	chr15:58941689..58944037-chr15:58949556..58952654,3	K562	blood:
19	chr15:58956671..58958559-chr15:58959977..58961761,2	K562	blood:
20	chr15:58959008..58961763-chr15:58963675..58966633,2	K562	blood:
21	chr15:58958405..58960158-chr15:58960218..58962844,2	MCF-7	breast:
22	chr15:58950082..58952311-chr15:58956735..58959470,2	K562	blood:
23	chr15:58953177..58955880-chr15:58958454..58961862,3	K562	blood:
24	chr15:58944978..58947722-chr15:58953875..58956765,2	K562	blood:
25	chr15:58938038..58940430-chr15:58949050..58951838,2	K562	blood:
26	chr15:58915714..58921238-chr15:58922986..58925558,6	K562	blood:
27	chr15:58928689..58931025-chr15:60688699..60690909,2	K562	blood:
28	chr15:58915714..58920888-chr15:58922126..58927407,8	K562	blood:
29	chr15:58950082..58952311-chr15:58956735..58959470,2	K562	blood:
30	chr15:58956671..58958559-chr15:58959977..58961761,2	K562	blood:
31	chr15:58932722..58935543-chr15:58957168..58958694,2	K562	blood:
32	chr15:58958405..58960158-chr15:58960218..58962844,2	MCF-7	breast:
33	chr15:58915714..58921238-chr15:58922986..58925558,6	K562	blood:
34	chr15:58944978..58947722-chr15:58953875..58956765,2	K562	blood:

Variant related genes	Relation type
ENSG00000270986	TF binding region
ADAM10	TF binding region
ENSG00000270986	CpG island
ADAM10	CpG island
ENSG00000137845	chromatin interactions
ENSG00000128923	chromatin interactions
ENSG00000270986	chromatin interactions
ENSG00000245975	chromatin interactions
ENSG00000182718	chromatin interactions

Extended variants
information (count: 2030 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:2030 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1427282	chr15:58914326-58914327	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs543421487	chr15:58914365-58914366	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs141165400	chr15:58914375-58914376	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs532305604	chr15:58914400-58914401	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs545680675	chr15:58914409-58914410	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs28415195	chr15:58914516-58914517	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs528226148	chr15:58914520-58914521	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs62002363	chr15:58914540-58914541	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs547182725	chr15:58914550-58914551	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs565428225	chr15:58914554-58914555	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs568028578	chr15:58914605-58914606	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs148263211	chr15:58914616-58914617	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs563035639	chr15:58914630-58914631	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs8043406	chr15:58914632-58914633	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs564234299	chr15:58914700-58914701	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs528270563	chr15:58914722-58914723	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs141425547	chr15:58914726-58914727	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs533587884	chr15:58914731-58914732	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs74378670	chr15:58914767-58914768	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs534869113	chr15:58914800-58914801	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs555064343	chr15:58914857-58914858	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs150390059	chr15:58914904-58914905	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs201628258	chr15:58914914-58914915	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs181324540	chr15:58914919-58914920	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs556974671	chr15:58914935-58914936	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs576821033	chr15:58914942-58914943	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs545694674	chr15:58914969-58914970	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs138401885	chr15:58914990-58914991	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs16940602	chr15:58915035-58915036	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs184423311	chr15:58915118-58915119	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs561899281	chr15:58915126-58915127	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs143908900	chr15:58915143-58915144	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs550687355	chr15:58915168-58915169	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs564119477	chr15:58915175-58915176	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs16940604	chr15:58915203-58915204	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs140897816	chr15:58915210-58915211	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs539851741	chr15:58915216-58915217	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs149440152	chr15:58915241-58915242	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs535302206	chr15:58915244-58915245	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs548531268	chr15:58915291-58915292	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs190003421	chr15:58915301-58915302	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs537192522	chr15:58915347-58915348	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs556988712	chr15:58915358-58915359	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs576835127	chr15:58915421-58915422	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs79135626	chr15:58915424-58915425	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs17236146	chr15:58915438-58915439	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs371181259	chr15:58915530-58915531	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs182231053	chr15:58915555-58915556	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs187154741	chr15:58915565-58915566	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs542092607	chr15:58915598-58915599	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

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
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17053054	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	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
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
Chronic lymphocytic leukemia	21546498	CNVD
Congenital diaphragmatic hernia	21341218	CNVD
Holoprosencephaly	21359414	CNVD
Myelofibrosis	22110671	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1580 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:58880600-58920600	Weak transcription	Skeletal Muscle Male	skeletal muscle
2	chr15:58888400-58920000	Weak transcription	Rectal Smooth Muscle	rectum
3	chr15:58889600-58919800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr15:58889800-58918800	Weak transcription	Osteobl	bone
5	chr15:58889800-58921000	Weak transcription	Ovary	ovary
6	chr15:58891400-58959600	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr15:58899200-58920200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
8	chr15:58901400-58918800	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr15:58903400-58918600	Weak transcription	HUVEC	blood vessel
10	chr15:58905000-58920800	Weak transcription	Left Ventricle	heart
11	chr15:58905000-58983200	Weak transcription	Esophagus	oesophagus
12	chr15:58905400-58919000	Weak transcription	NHEK	skin
13	chr15:58905400-58919600	Weak transcription	Rectal Mucosa Donor 31	rectum
14	chr15:58905400-58971800	Weak transcription	Spleen	Spleen
15	chr15:58905600-58919800	Weak transcription	Stomach Mucosa	stomach
16	chr15:58905600-58976400	Weak transcription	Gastric	stomach
17	chr15:58906400-58915200	Weak transcription	HSMMtube	muscle
18	chr15:58906400-58920000	Weak transcription	Colonic Mucosa	Colon
19	chr15:58906400-58923000	Weak transcription	Pancreas	Pancrea
20	chr15:58906400-58976400	Weak transcription	Small Intestine	intestine
21	chr15:58907000-58918800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr15:58907200-58914800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
23	chr15:58907200-58914800	Strong transcription	Monocytes-CD14+_RO01746	blood
24	chr15:58907200-58915000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
25	chr15:58907200-58918800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr15:58907200-58918800	Weak transcription	Skeletal Muscle Female	skeletal muscle
27	chr15:58907200-58919200	Weak transcription	HepG2	liver
28	chr15:58907200-58919200	Weak transcription	NHLF	lung
29	chr15:58907200-58919400	Weak transcription	Brain Cingulate Gyrus	brain
30	chr15:58907200-58919400	Weak transcription	Colon Smooth Muscle	Colon
31	chr15:58907200-58920000	Weak transcription	Brain Inferior Temporal Lobe	brain
32	chr15:58907200-58920600	Weak transcription	Stomach Smooth Muscle	stomach
33	chr15:58907200-58920800	Weak transcription	NH-A	brain
34	chr15:58907400-58916200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr15:58907400-58920800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr15:58907800-58952000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr15:58908000-58917800	Weak transcription	Fetal Muscle Trunk	muscle
38	chr15:58908000-58923000	Weak transcription	Sigmoid Colon	Sigmoid Colon
39	chr15:58908400-58918200	Weak transcription	Rectal Mucosa Donor 29	rectum
40	chr15:58908600-58918800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr15:58908600-58920000	Weak transcription	Duodenum Smooth Muscle	Duodenum
42	chr15:58909000-58918600	Weak transcription	Cortex derived primary cultured neurospheres	brain
43	chr15:58909000-58920800	Weak transcription	Hela-S3	cervix
44	chr15:58910400-58923200	Weak transcription	Lung	lung
45	chr15:58910400-58934000	Weak transcription	Psoas Muscle	Psoas
46	chr15:58910600-58917600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr15:58910600-58918000	Weak transcription	NHDF-Ad	bronchial
48	chr15:58910800-58915400	Weak transcription	Right Ventricle	heart
49	chr15:58910800-58918000	Weak transcription	Brain Germinal Matrix	brain
50	chr15:58910800-58926200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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