Variant report

Variant	nsv569235
Chromosome Location	chr15:42304628-42326259
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:130)
CpG islands
(count:183)
Chromatin interactive
region (count:16)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:130 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr15:42319658-42319825	K562	blood:	n/a	n/a
2	BCL3	chr15:42325081-42325411	GM12878	blood:	n/a	n/a
3	BCL3	chr15:42305579-42305815	GM12878	blood:	n/a	n/a
4	BCL3	chr15:42305567-42305938	GM12878	blood:	n/a	n/a
5	BCL3	chr15:42324897-42325492	GM12878	blood:	n/a	n/a
6	BHLHE40	chr15:42325255-42325311	HepG2	liver:	n/a	n/a
7	CBX3	chr15:42317289-42317567	K562	blood:	n/a	n/a
8	CBX3	chr15:42317325-42317560	K562	blood:	n/a	n/a
9	CEBPB	chr15:42310910-42311191	IMR90	lung:	n/a	chr15:42311048-42311059
10	CEBPB	chr15:42304520-42304687	HepG2	liver:	n/a	chr15:42304627-42304638
11	CEBPB	chr15:42310946-42311120	H1-hESC	embryonic stem cell:	n/a	chr15:42311048-42311059
12	CEBPB	chr15:42310941-42311185	K562	blood:	n/a	chr15:42311048-42311059
13	CEBPB	chr15:42310893-42311207	A549	lung:	n/a	chr15:42311048-42311059
14	CEBPB	chr15:42313722-42313882	HepG2	liver:	n/a	chr15:42313766-42313777 chr15:42313768-42313779
15	CEBPB	chr15:42304404-42304735	HepG2	liver:	n/a	chr15:42304627-42304638
16	CEBPB	chr15:42304420-42304802	HepG2	liver:	n/a	chr15:42304627-42304638
17	CEBPB	chr15:42310869-42311214	HepG2	liver:	n/a	chr15:42311048-42311059
18	CEBPB	chr15:42320148-42320349	HepG2	liver:	n/a	n/a
19	CEBPB	chr15:42304573-42304630	K562	blood:	n/a	n/a
20	CEBPB	chr15:42311003-42311089	Hela-S3	cervix:	n/a	chr15:42311048-42311059
21	CTCF	chr15:42314091-42314096	Kidney_OC	kidney:	n/a	n/a
22	CTCF	chr15:42310860-42311010	BE2_C	brain:	n/a	n/a
23	CTCF	chr15:42313460-42313610	GM12865	blood:	n/a	n/a
24	CTCF	chr15:42310940-42311090	WERI-Rb-1	eye:	n/a	n/a
25	CTCF	chr15:42310900-42311050	SK-N-SH_RA	brain:	n/a	n/a
26	CTCF	chr15:42310960-42311110	NHEK	skin:	n/a	n/a
27	CTCF	chr15:42310900-42311050	BE2_C	brain:	n/a	n/a
28	CTCF	chr15:42313222-42313322	NHEK	skin:	n/a	n/a
29	CTCF	chr15:42313220-42313370	SAEC	small airway:	n/a	n/a
30	EBF1	chr15:42306827-42307293	GM12878	blood:	n/a	chr15:42307095-42307105 chr15:42307093-42307106 chr15:42307094-42307105 chr15:42306884-42306894 chr15:42307095-42307104
31	EBF1	chr15:42306996-42307194	GM12878	blood:	n/a	chr15:42307095-42307105 chr15:42307093-42307106 chr15:42307094-42307105 chr15:42307095-42307104
32	EBF1	chr15:42325361-42325860	GM12878	blood:	n/a	chr15:42325546-42325559 chr15:42325547-42325558
33	EBF1	chr15:42324949-42325987	GM12878	blood:	n/a	chr15:42325546-42325559 chr15:42325547-42325558
34	EBF1	chr15:42325392-42325802	GM12878	blood:	n/a	chr15:42325546-42325559 chr15:42325547-42325558
35	ELF1	chr15:42304416-42304673	HepG2	liver:	n/a	chr15:42304529-42304540
36	ELF1	chr15:42304375-42304723	HepG2	liver:	n/a	chr15:42304529-42304540
37	EP300	chr15:42317675-42317822	K562	blood:	n/a	n/a
38	EP300	chr15:42325268-42325600	GM12878	blood:	n/a	n/a
39	FOS	chr15:42316743-42316916	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr15:42316615-42316946	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr15:42313154-42313468	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr15:42304964-42305070	MCF10A-Er-Src	breast:	n/a	chr15:42305028-42305036 chr15:42305024-42305035 chr15:42305029-42305036
43	FOS	chr15:42322302-42322323	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr15:42317561-42317582	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr15:42313153-42313420	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr15:42316686-42316881	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr15:42304663-42304664	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr15:42304502-42304634	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr15:42323839-42324146	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr15:42313161-42313431	MCF10A-Er-Src	breast:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:42308263-42308313	GM12878	blood:	n/a
2	chr15:42308160-42308210	NHBE	bronchial:	n/a
3	chr15:42308205-42308255	HCF	heart:	n/a
4	chr15:42308205-42308255	ProgFib	skin:	n/a
5	chr15:42308263-42308313	BE2_C	brain:	n/a
6	chr15:42308205-42308255	HRPEpiC	eye:	n/a
7	chr15:42308160-42308210	HMEC	breast:	n/a
8	chr15:42308263-42308313	ovcar-3	ovarian:	n/a
9	chr15:42308263-42308313	BJ	skin:	n/a
10	chr15:42308205-42308255	NB4	blood:	n/a
11	chr15:42308160-42308210	HCM	heart:	n/a
12	chr15:42308205-42308255	NHBE	bronchial:	n/a
13	chr15:42308263-42308313	MCF-7	breast:	n/a
14	chr15:42308205-42308255	PFSK-1	brain:	n/a
15	chr15:42308160-42308210	Hela-S3	cervix:	n/a
16	chr15:42308263-42308313	HRCEpiC	kidney:	n/a
17	chr15:42308263-42308313	HCF	heart:	n/a
18	chr15:42308205-42308255	AG09309	skin:	n/a
19	chr15:42308263-42308313	HCM	heart:	n/a
20	chr15:42308205-42308255	CMK	blood:	n/a
21	chr15:42308205-42308255	A549	lung:	n/a
22	chr15:42308205-42308255	HEEpiC	esophagus:	n/a
23	chr15:42308205-42308255	ovcar-3	ovarian:	n/a
24	chr15:42308160-42308210	SKMC	muscle:	n/a
25	chr15:42308263-42308313	RPTEC	kidney:	n/a
26	chr15:42308160-42308210	PFSK-1	brain:	n/a
27	chr15:42308160-42308210	GM12878	blood:	n/a
28	chr15:42308205-42308255	HMEC	breast:	n/a
29	chr15:42308205-42308255	BJ	skin:	n/a
30	chr15:42308205-42308255	SK-N-MC	brain:	n/a
31	chr15:42308263-42308313	HMEC	breast:	n/a
32	chr15:42308263-42308313	Hepatocyte	liver:	n/a
33	chr15:42308205-42308255	RPTEC	kidney:	n/a
34	chr15:42308263-42308313	AG10803	skin:	n/a
35	chr15:42308263-42308313	PFSK-1	brain:	n/a
36	chr15:42308263-42308313	AoSMC	blood vessel:	n/a
37	chr15:42308205-42308255	BE2_C	brain:	n/a
38	chr15:42308160-42308210	GM06990	blood:	n/a
39	chr15:42308205-42308255	U87	brain:	n/a
40	chr15:42308263-42308313	MCF10A-Er-Src	breast:	n/a
41	chr15:42308263-42308313	SK-N-SH_RA	brain:	n/a
42	chr15:42308263-42308313	NB4	blood:	n/a
43	chr15:42308263-42308313	PrEC	prostate:	n/a
44	chr15:42308263-42308313	HEEpiC	esophagus:	n/a
45	chr15:42308263-42308313	H1-hESC	embryonic stem cell:	embryo
46	chr15:42308160-42308210	HRPEpiC	eye:	n/a
47	chr15:42308160-42308210	HAEpiC	amniotic membrane:	n/a
48	chr15:42308263-42308313	SAEC	small airway:	n/a
49	chr15:42308205-42308255	HL-60	blood:	n/a
50	chr15:42308263-42308313	HEK293	kidney:	embryo

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:42302877..42304522-chr15:42314324..42316672,2	MCF-7	breast:
2	chr15:42290890..42293592-chr15:42305193..42306986,2	K562	blood:
3	chr15:42313023..42314769-chr15:42339257..42341704,2	K562	blood:
4	chr15:42318244..42322022-chr15:42323761..42326594,4	K562	blood:
5	chr15:42305912..42307949-chr15:42313867..42316422,2	MCF-7	breast:
6	chr15:42295229..42297667-chr15:42310261..42312027,2	K562	blood:
7	chr15:42321125..42324302-chr15:42342047..42344637,3	K562	blood:
8	chr15:42318931..42321446-chr15:42351277..42353565,2	K562	blood:
9	chr15:42301533..42304416-chr15:42306961..42309245,2	K562	blood:
10	chr15:42281486..42282251-chr15:42325577..42326393,2	MCF-7	breast:
11	chr15:42313009..42314884-chr15:42328123..42329860,2	K562	blood:
12	chr15:42294519..42296729-chr15:42308875..42311761,2	K562	blood:
13	chr15:42301860..42304416-chr15:42306961..42309599,2	K562	blood:
14	chr15:42305912..42307949-chr15:42313867..42316422,2	MCF-7	breast:
15	chr15:42318244..42322022-chr15:42323761..42326594,4	K562	blood:
16	chr15:42296975..42299323-chr15:42309819..42311922,2	MCF-7	breast:

No data

Variant related genes	Relation type
PLA2G4E	TF binding region
PLA2G4E	CpG island
ENSG00000188089	chromatin interactions
ENSG00000257797	chromatin interactions

Extended variants
information (count: 933 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:933 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11632711	chr15:42304628-42304629	Enhancers Genic enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs74578540	chr15:42304644-42304645	Enhancers Genic enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs4924602	chr15:42304698-42304699	Enhancers Genic enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs553669957	chr15:42304712-42304713	Enhancers Genic enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs556699700	chr15:42304753-42304754	Enhancers Genic enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs573355153	chr15:42304795-42304796	Enhancers Genic enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs578189905	chr15:42304869-42304870	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs545538406	chr15:42304898-42304899	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs144444934	chr15:42304900-42304901	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs116514651	chr15:42304905-42304906	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs544744942	chr15:42304969-42304970	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs188110880	chr15:42304977-42304978	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs12439430	chr15:42305042-42305043	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	mRNA abundance
14	rs549000696	chr15:42305114-42305115	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs56725574	chr15:42305118-42305119	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs28438695	chr15:42305165-42305166	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs551521617	chr15:42305236-42305237	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs527967617	chr15:42305246-42305247	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs536729771	chr15:42305308-42305309	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs148050411	chr15:42305347-42305348	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs368824718	chr15:42305357-42305358	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs72726085	chr15:42305382-42305383	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs552028858	chr15:42305451-42305452	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs192939821	chr15:42305477-42305478	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs73397812	chr15:42305484-42305485	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs183562489	chr15:42305493-42305494	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs543857868	chr15:42305497-42305498	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs573444693	chr15:42305500-42305501	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs141810501	chr15:42305528-42305529	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs80087064	chr15:42305539-42305540	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs575941041	chr15:42305541-42305542	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs367589889	chr15:42305546-42305547	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs552657653	chr15:42305568-42305569	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs561413400	chr15:42305579-42305580	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs574839190	chr15:42305593-42305594	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs540580022	chr15:42305594-42305595	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs188896442	chr15:42305639-42305640	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs528361481	chr15:42305642-42305643	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs551291301	chr15:42305679-42305680	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs564723366	chr15:42305693-42305694	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs1628549	chr15:42305698-42305699	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs16972456	chr15:42305726-42305727	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs566978013	chr15:42305740-42305741	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs535976123	chr15:42305766-42305767	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs386783435	chr15:42305769-42305770	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs76383211	chr15:42305770-42305771	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs62004282	chr15:42305773-42305774	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs113860755	chr15:42305775-42305776	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs1668566	chr15:42305777-42305778	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs62004283	chr15:42305778-42305779	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:68)

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
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:193 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:42290400-42310400	Weak transcription	Right Atrium	heart
2	chr15:42301800-42306000	Enhancers	Fetal Intestine Small	intestine
3	chr15:42302000-42305400	Enhancers	Placenta	Placenta
4	chr15:42302000-42306000	Enhancers	Fetal Intestine Large	intestine
5	chr15:42303600-42304800	Enhancers	GM12878-XiMat	blood
6	chr15:42303600-42305000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr15:42303600-42309000	Weak transcription	Skeletal Muscle Female	skeletal muscle
8	chr15:42303800-42305400	Weak transcription	Lung	lung
9	chr15:42304000-42305000	Enhancers	Duodenum Mucosa	Duodenum
10	chr15:42304000-42305000	Enhancers	Rectal Mucosa Donor 31	rectum
11	chr15:42304000-42305400	Enhancers	Pancreas	Pancrea
12	chr15:42304000-42305600	Enhancers	Stomach Mucosa	stomach
13	chr15:42304200-42304800	Enhancers	Sigmoid Colon	Sigmoid Colon
14	chr15:42304200-42305000	Enhancers	Colonic Mucosa	Colon
15	chr15:42304200-42305400	Enhancers	Esophagus	oesophagus
16	chr15:42304200-42305400	Enhancers	Rectal Mucosa Donor 29	rectum
17	chr15:42304400-42305200	Enhancers	HepG2	liver
18	chr15:42304400-42305600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr15:42304600-42304800	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr15:42304600-42305200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr15:42304600-42305400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr15:42304600-42305400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr15:42304600-42305800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
24	chr15:42304800-42305000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr15:42305000-42305600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr15:42305000-42305600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr15:42305400-42307200	Enhancers	Lung	lung
28	chr15:42305400-42312800	Weak transcription	Esophagus	oesophagus
29	chr15:42305600-42312600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr15:42305800-42306000	Enhancers	Spleen	Spleen
31	chr15:42306000-42310600	Weak transcription	Spleen	Spleen
32	chr15:42307200-42307400	Enhancers	Psoas Muscle	Psoas
33	chr15:42307200-42313200	Weak transcription	Lung	lung
34	chr15:42307600-42307800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
35	chr15:42309000-42309600	Enhancers	Fetal Muscle Trunk	muscle
36	chr15:42309000-42310400	Enhancers	Skeletal Muscle Female	skeletal muscle
37	chr15:42309000-42312800	Enhancers	Fetal Muscle Leg	muscle
38	chr15:42309200-42310000	Enhancers	Psoas Muscle	Psoas
39	chr15:42309200-42310200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
40	chr15:42309400-42309600	Enhancers	Right Ventricle	heart
41	chr15:42309400-42312800	Enhancers	Skeletal Muscle Male	skeletal muscle
42	chr15:42309600-42310600	Weak transcription	Fetal Muscle Trunk	muscle
43	chr15:42309600-42310600	Weak transcription	Right Ventricle	heart
44	chr15:42309800-42311800	Enhancers	Fetal Lung	lung
45	chr15:42310000-42310400	Weak transcription	Psoas Muscle	Psoas
46	chr15:42310200-42311800	Enhancers	Breast Myoepithelial Primary Cells	Breast
47	chr15:42310200-42311800	Enhancers	Placenta	Placenta
48	chr15:42310200-42312000	Enhancers	Fetal Heart	heart
49	chr15:42310400-42311400	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
50	chr15:42310400-42312000	Enhancers	Psoas Muscle	Psoas

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