Variant report

Variant	nsv569404
Chromosome Location	chr15:51234595-51294995
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:184)
CpG islands
(count:244)
Chromatin interactive
region (count:33)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:184 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr15:51252287-51252483	GM12878	blood:	n/a	n/a
2	BATF	chr15:51252266-51252532	GM12878	blood:	n/a	n/a
3	CBX3	chr15:51256264-51256639	K562	blood:	n/a	n/a
4	CBX3	chr15:51256286-51256609	K562	blood:	n/a	n/a
5	CBX3	chr15:51253479-51253816	K562	blood:	n/a	n/a
6	CBX3	chr15:51254487-51254771	K562	blood:	n/a	n/a
7	CEBPB	chr15:51238825-51238955	A549	lung:	n/a	n/a
8	CEBPB	chr15:51245421-51245826	HCT-116	colon:	n/a	chr15:51245660-51245671
9	CEBPB	chr15:51293580-51293768	HepG2	liver:	n/a	chr15:51293623-51293634
10	CEBPB	chr15:51288894-51289247	IMR90	lung:	n/a	n/a
11	CEBPB	chr15:51260477-51261026	A549	lung:	n/a	n/a
12	CEBPB	chr15:51260640-51260842	A549	lung:	n/a	n/a
13	CEBPB	chr15:51245571-51245835	Hela-S3	cervix:	n/a	chr15:51245660-51245671
14	CEBPB	chr15:51260564-51260861	A549	lung:	n/a	n/a
15	CEBPB	chr15:51235889-51236211	IMR90	lung:	n/a	n/a
16	CEBPB	chr15:51245498-51245891	IMR90	lung:	n/a	chr15:51245660-51245671
17	CEBPB	chr15:51260618-51260908	IMR90	lung:	n/a	n/a
18	CEBPB	chr15:51293551-51293682	K562	blood:	n/a	chr15:51293623-51293634
19	CEBPB	chr15:51245553-51245824	HepG2	liver:	n/a	chr15:51245660-51245671
20	CEBPB	chr15:51259457-51259644	A549	lung:	n/a	n/a
21	CTCF	chr15:51236160-51236310	A549	lung:	n/a	n/a
22	CTCF	chr15:51294147-51294193	A549	lung:	n/a	n/a
23	CTCF	chr15:51236271-51236458	MCF-7	breast:	n/a	n/a
24	CTCF	chr15:51236280-51236430	MCF-7	breast:	n/a	n/a
25	CTCF	chr15:51257460-51257610	GM12874	blood:	n/a	n/a
26	CTCF	chr15:51236213-51236618	MCF-7	breast:	n/a	n/a
27	CTCF	chr15:51236220-51236370	HMEC	breast:	n/a	n/a
28	CTCF	chr15:51274260-51274410	GM12864	blood:	n/a	n/a
29	CTCF	chr15:51261846-51261909	Kidney_OC	kidney:	n/a	n/a
30	CTCF	chr15:51236300-51236450	HMEC	breast:	n/a	n/a
31	CTCF	chr15:51236220-51236370	HRE	kidney:	n/a	n/a
32	CTCF	chr15:51236361-51236377	GM12878	blood:	n/a	n/a
33	CTCF	chr15:51236333-51236377	Pancreas_OC	pancreas:	n/a	n/a
34	CTCF	chr15:51236298-51236435	MCF-7	breast:	n/a	n/a
35	CTCF	chr15:51236200-51236350	MCF-7	breast:	n/a	n/a
36	CTCF	chr15:51273140-51273290	HRE	kidney:	n/a	n/a
37	CTCF	chr15:51271265-51271307	K562	blood:	n/a	n/a
38	CTCF	chr15:51247940-51248090	GM12866	blood:	n/a	n/a
39	CTCF	chr15:51241900-51242050	GM12872	blood:	n/a	n/a
40	CTCF	chr15:51236220-51236370	HPF	lung:	n/a	n/a
41	CTCF	chr15:51236253-51236515	GM12878	blood:	n/a	n/a
42	CTCF	chr15:51236333-51236371	K562	blood:	n/a	n/a
43	CTCF	chr15:51255800-51255950	GM06990	blood:	n/a	n/a
44	E2F4	chr15:51294144-51294147	MCF10A-Er-Src	breast:	n/a	n/a
45	E2F4	chr15:51245702-51246021	MCF10A-Er-Src	breast:	n/a	n/a
46	E2F4	chr15:51235980-51236191	MCF10A-Er-Src	breast:	n/a	n/a
47	E2F4	chr15:51285877-51286056	MCF10A-Er-Src	breast:	n/a	n/a
48	EBF1	chr15:51283507-51283732	GM12878	blood:	n/a	chr15:51283611-51283621 chr15:51283611-51283622
49	ELK1	chr15:51257275-51257294	Hela-S3	cervix:	n/a	n/a
50	EP300	chr15:51282055-51282135	K562	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:51235757-51235807	HIPEpiC	eye:	n/a
2	chr15:51235757-51235807	HRCEpiC	kidney:	n/a
3	chr15:51236304-51236354	HepG2	liver:	n/a
4	chr15:51243589-51243639	PFSK-1	brain:	n/a
5	chr15:51235757-51235807	GM12891	blood:	n/a
6	chr15:51236304-51236354	SK-N-MC	brain:	n/a
7	chr15:51236304-51236354	T-47D	breast:	n/a
8	chr15:51235727-51235777	HCT-116	colon:	n/a
9	chr15:51235727-51235777	HCF	heart:	n/a
10	chr15:51235757-51235807	HUVEC	blood vessel:	n/a
11	chr15:51243589-51243639	HCT-116	colon:	n/a
12	chr15:51243589-51243639	SAEC	small airway:	n/a
13	chr15:51235727-51235777	IMR90	lung:	fetal
14	chr15:51236304-51236354	NHBE	bronchial:	n/a
15	chr15:51243589-51243639	GM12892	blood:	n/a
16	chr15:51236304-51236354	HRPEpiC	eye:	n/a
17	chr15:51243589-51243639	AG10803	skin:	n/a
18	chr15:51235727-51235777	PrEC	prostate:	n/a
19	chr15:51243589-51243639	BE2_C	brain:	n/a
20	chr15:51243589-51243639	HCM	heart:	n/a
21	chr15:51236304-51236354	HUVEC	blood vessel:	n/a
22	chr15:51235757-51235807	AG09319	gingival:	n/a
23	chr15:51243589-51243639	IMR90	lung:	fetal
24	chr15:51235757-51235807	RPTEC	kidney:	n/a
25	chr15:51236304-51236354	IMR90	lung:	fetal
26	chr15:51235757-51235807	ProgFib	skin:	n/a
27	chr15:51243589-51243639	CMK	blood:	n/a
28	chr15:51236304-51236354	NB4	blood:	n/a
29	chr15:51236304-51236354	Hepatocyte	liver:	n/a
30	chr15:51235757-51235807	NH-A	brain:	n/a
31	chr15:51235757-51235807	HRE	kidney:	n/a
32	chr15:51236304-51236354	NH-A	brain:	n/a
33	chr15:51235757-51235807	BJ	skin:	n/a
34	chr15:51235757-51235807	HMEC	breast:	n/a
35	chr15:51243589-51243639	Jurkat	blood:	n/a
36	chr15:51235757-51235807	CMK	blood:	n/a
37	chr15:51235727-51235777	HRCEpiC	kidney:	n/a
38	chr15:51235727-51235777	HRPEpiC	eye:	n/a
39	chr15:51235727-51235777	HIPEpiC	eye:	n/a
40	chr15:51235757-51235807	AG10803	skin:	n/a
41	chr15:51236304-51236354	Caco-2	colon:	n/a
42	chr15:51236304-51236354	SK-N-SH	brain:	n/a
43	chr15:51235757-51235807	NHDF-neo	bronchial:	n/a
44	chr15:51243589-51243639	GM12891	blood:	n/a
45	chr15:51235727-51235777	Hepatocyte	liver:	n/a
46	chr15:51235727-51235777	GM06990	blood:	n/a
47	chr15:51235727-51235777	SAEC	small airway:	n/a
48	chr15:51236304-51236354	CMK	blood:	n/a
49	chr15:51243589-51243639	PANC-1	pancreas:	n/a
50	chr15:51235757-51235807	AoSMC	blood vessel:	n/a

(count:33 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:51242549..51245131-chr15:51257817..51260638,2	MCF-7	breast:
2	chr15:51293258..51295626-chr15:51337830..51340357,2	MCF-7	breast:
3	chr15:51265611..51268548-chr15:51273285..51275187,2	MCF-7	breast:
4	chr15:51291454..51293095-chr15:51294731..51296517,2	K562	blood:
5	chr15:51248351..51249869-chr15:51253170..51254880,2	MCF-7	breast:
6	chr1:121484254..121485225-chr15:51241675..51242617,2	MCF-7	breast:
7	chr15:51242549..51245131-chr15:51257817..51260638,2	MCF-7	breast:
8	chr15:51255834..51257399-chr15:51273683..51276237,2	MCF-7	breast:
9	chr15:51275789..51278184-chr15:51333901..51335893,2	MCF-7	breast:
10	chr15:51230290..51232178-chr15:51234294..51236150,2	MCF-7	breast:
11	chr15:51237490..51239996-chr15:51331405..51333365,2	MCF-7	breast:
12	chr15:51269282..51271249-chr15:51274355..51276243,2	MCF-7	breast:
13	chr15:51229240..51231404-chr15:51232886..51235575,2	K562	blood:
14	chr15:51255834..51257399-chr15:51273683..51276237,2	MCF-7	breast:
15	chr15:51240708..51242711-chr15:51242889..51245874,2	K562	blood:
16	chr15:51243593..51246491-chr15:51256296..51259050,2	MCF-7	breast:
17	chr15:51248351..51249869-chr15:51253170..51254880,2	MCF-7	breast:
18	chr15:51275705..51277653-chr15:51278587..51281161,2	MCF-7	breast:
19	chr15:51240708..51242711-chr15:51242889..51245874,2	K562	blood:
20	chr15:51288949..51290565-chr15:51293447..51295234,3	MCF-7	breast:
21	chr15:51280912..51283602-chr15:51286320..51288596,2	MCF-7	breast:
22	chr15:51275705..51277653-chr15:51278587..51281161,2	MCF-7	breast:
23	chr15:51243593..51246491-chr15:51256296..51259050,2	MCF-7	breast:
24	chr15:51280912..51283602-chr15:51286320..51288596,2	MCF-7	breast:
25	chr15:51234956..51237517-chr15:51240627..51243200,3	K562	blood:
26	chr15:51259926..51261571-chr15:51483708..51485228,2	MCF-7	breast:
27	chr15:51265611..51268548-chr15:51273285..51275187,2	MCF-7	breast:
28	chr15:51291205..51293586-chr15:51295026..51296629,2	MCF-7	breast:
29	chr15:51291454..51293095-chr15:51294731..51296517,2	K562	blood:
30	chr15:51236074..51236844-chr15:51484819..51485462,2	MCF-7	breast:
31	chr15:51294396..51297961-chr15:51303486..51306032,4	MCF-7	breast:
32	chr15:51269282..51271249-chr15:51274355..51276243,2	MCF-7	breast:
33	chr15:51213388..51216180-chr15:51233537..51235564,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GLDN-5	chr15:51236326-51238762	NONHSAT042446
2	lnc-GLDN-5	chr15:51236860-51238193	NONHSAT042447

No data

Variant related genes	Relation type
AP4E1	TF binding region
DCAF13P3	TF binding region
AP4E1	CpG island
DCAF13P3	CpG island
ENSG00000259378	chromatin interactions
ENSG00000081014	chromatin interactions

Extended variants
information (count: 2213 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:2213 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9944192	chr15:51234595-51234596	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs182589818	chr15:51234672-51234673	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs540550366	chr15:51234681-51234682	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs537210605	chr15:51234710-51234711	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs187828683	chr15:51234721-51234722	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs191895089	chr15:51234768-51234769	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs576579415	chr15:51234770-51234771	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs551345870	chr15:51234798-51234799	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs540749856	chr15:51234801-51234802	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs530630508	chr15:51234842-51234843	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs559313630	chr15:51234947-51234948	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs372421281	chr15:51234984-51234985	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs574322439	chr15:51235041-51235042	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs202145123	chr15:51235093-51235094	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs542107195	chr15:51235097-51235098	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs183636409	chr15:51235200-51235201	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs188625018	chr15:51235209-51235210	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs552445745	chr15:51235273-51235274	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs377170036	chr15:51235280-51235281	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs146989789	chr15:51235350-51235351	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs77944312	chr15:51235440-51235441	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs192625435	chr15:51235457-51235458	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs1871460	chr15:51235469-51235470	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs184830970	chr15:51235519-51235520	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs566086834	chr15:51235520-51235521	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs537633445	chr15:51235659-51235660	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs536207082	chr15:51235682-51235683	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs72744303	chr15:51235835-51235836	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs186850156	chr15:51235839-51235840	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs537348228	chr15:51235862-51235863	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs550274984	chr15:51235863-51235864	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs558756668	chr15:51235896-51235897	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs371512736	chr15:51235899-51235900	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs137964040	chr15:51235920-51235921	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs534734826	chr15:51235937-51235938	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs552745491	chr15:51235974-51235975	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs191258761	chr15:51235992-51235993	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs541501362	chr15:51235993-51235994	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs184895853	chr15:51236032-51236033	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs375062801	chr15:51236058-51236059	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs575638672	chr15:51236269-51236270	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs8031702	chr15:51236304-51236305	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs189777075	chr15:51236316-51236317	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
44	rs528246096	chr15:51236337-51236338	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
45	rs143537761	chr15:51236350-51236351	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
46	rs76253543	chr15:51236352-51236353	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
47	rs181261149	chr15:51236375-51236376	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
48	rs115453920	chr15:51236409-51236410	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
49	rs569695614	chr15:51236412-51236413	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
50	rs537385021	chr15:51236417-51236418	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region lncRNA	1 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
Breast cancer	21785460	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
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Myelofibrosis	22110671	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1977 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:51201600-51243200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr15:51201600-51245000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr15:51201800-51242800	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr15:51201800-51248400	Weak transcription	Colonic Mucosa	Colon
5	chr15:51201800-51271600	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr15:51202600-51236800	Weak transcription	Small Intestine	intestine
7	chr15:51202600-51241800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
8	chr15:51202600-51242800	Weak transcription	Gastric	stomach
9	chr15:51202800-51243400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr15:51203200-51242200	Weak transcription	Brain Substantia Nigra	brain
11	chr15:51203200-51242800	Weak transcription	Lung	lung
12	chr15:51203400-51242400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
13	chr15:51204800-51243000	Strong transcription	Monocytes-CD14+_RO01746	blood
14	chr15:51205600-51242800	Weak transcription	Placenta Amnion	Placenta Amnion
15	chr15:51205800-51249000	Weak transcription	Fetal Brain Male	brain
16	chr15:51205800-51254400	Weak transcription	Fetal Heart	heart
17	chr15:51208000-51250400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
18	chr15:51208400-51242200	Weak transcription	Fetal Kidney	kidney
19	chr15:51210400-51243000	Weak transcription	Brain Angular Gyrus	brain
20	chr15:51210600-51298400	Weak transcription	Stomach Mucosa	stomach
21	chr15:51213000-51242800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr15:51213200-51245400	Weak transcription	Psoas Muscle	Psoas
23	chr15:51213600-51243400	Weak transcription	Pancreas	Pancrea
24	chr15:51213800-51247600	Weak transcription	Aorta	Aorta
25	chr15:51214600-51236800	Weak transcription	Rectal Smooth Muscle	rectum
26	chr15:51214600-51247800	Weak transcription	Esophagus	oesophagus
27	chr15:51219800-51243000	Weak transcription	Brain Hippocampus Middle	brain
28	chr15:51220000-51242200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr15:51220200-51236800	Weak transcription	Right Ventricle	heart
30	chr15:51220200-51243000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
31	chr15:51221800-51242200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr15:51221800-51242400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
33	chr15:51221800-51242800	Weak transcription	Brain Anterior Caudate	brain
34	chr15:51222000-51236200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
35	chr15:51222000-51242800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
36	chr15:51223400-51236200	Weak transcription	HUES64 Cell Line	embryonic stem cell
37	chr15:51223400-51243000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
38	chr15:51223400-51243000	Weak transcription	Brain Cingulate Gyrus	brain
39	chr15:51225000-51236800	Weak transcription	HUES48 Cell Line	embryonic stem cell
40	chr15:51225000-51242200	Weak transcription	Skeletal Muscle Male	skeletal muscle
41	chr15:51225200-51236400	Weak transcription	Cortex derived primary cultured neurospheres	brain
42	chr15:51225200-51236800	Weak transcription	HMEC	breast
43	chr15:51225200-51237000	Weak transcription	Duodenum Smooth Muscle	Duodenum
44	chr15:51225800-51236000	Weak transcription	GM12878-XiMat	blood
45	chr15:51226000-51240600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr15:51226000-51242400	Weak transcription	Rectal Mucosa Donor 31	rectum
47	chr15:51228800-51236400	Weak transcription	Primary B cells from cord blood	blood
48	chr15:51230400-51236400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
49	chr15:51230400-51236600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr15:51230800-51235000	Weak transcription	Duodenum Mucosa	Duodenum

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