Variant report

Variant	nsv827315
Chromosome Location	chr15:45318832-45323951
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:65)
CpG islands
(count:61)
Chromatin interactive
region (count:1)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:65 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:45319667-45319860	K562	blood:	n/a	n/a
2	ATF1	chr15:45321173-45321223	K562	blood:	n/a	n/a
3	CBX3	chr15:45323934-45324441	K562	blood:	n/a	n/a
4	CBX3	chr15:45323759-45324400	K562	blood:	n/a	n/a
5	CBX3	chr15:45321710-45322207	K562	blood:	n/a	n/a
6	CBX3	chr15:45321842-45322070	K562	blood:	n/a	n/a
7	CEBPB	chr15:45322965-45323330	K562	blood:	n/a	chr15:45323141-45323152
8	CEBPB	chr15:45322992-45323243	K562	blood:	n/a	chr15:45323141-45323152
9	CEBPB	chr15:45323012-45323267	HepG2	liver:	n/a	chr15:45323141-45323152
10	CEBPB	chr15:45319580-45319770	K562	blood:	n/a	n/a
11	CEBPB	chr15:45323785-45324250	K562	blood:	n/a	n/a
12	CEBPD	chr15:45323757-45324332	K562	blood:	n/a	n/a
13	CTCF	chr15:45318900-45319050	RPTEC	kidney:	n/a	n/a
14	CTCF	chr15:45318700-45318850	HPAF	blood vessel:	n/a	n/a
15	EP300	chr15:45318795-45320180	SK-N-SH	brain:	n/a	chr15:45319152-45319166
16	EP300	chr15:45319562-45319752	K562	blood:	n/a	n/a
17	EP300	chr15:45320383-45321549	SK-N-SH	brain:	n/a	chr15:45321423-45321437 chr15:45321424-45321433 chr15:45321284-45321298
18	FAM48A	chr15:45323542-45323666	GM12878	blood:	n/a	n/a
19	GATA1	chr15:45323639-45324008	PBDE	blood:	n/a	chr15:45323963-45323979 chr15:45323963-45323979
20	GATA2	chr15:45320990-45321321	SH-SY5Y	brain:	n/a	n/a
21	GATA2	chr15:45318863-45319238	HUVEC	blood vessel:	n/a	chr15:45319014-45319024 chr15:45319014-45319021 chr15:45319154-45319165
22	GATA2	chr15:45323697-45324456	K562	blood:	n/a	chr15:45324075-45324084 chr15:45324027-45324043 chr15:45323963-45323979 chr15:45323963-45323979
23	GATA3	chr15:45320956-45321396	SH-SY5Y	brain:	n/a	n/a
24	JUND	chr15:45319377-45319804	K562	blood:	n/a	n/a
25	KAP1	chr15:45321685-45322280	K562	blood:	n/a	n/a
26	MAFF	chr15:45319522-45319729	K562	blood:	n/a	n/a
27	MAZ	chr15:45319007-45319282	K562	blood:	n/a	n/a
28	MYC	chr15:45319526-45319719	K562	blood:	n/a	n/a
29	NR2F2	chr15:45323755-45324354	K562	blood:	n/a	n/a
30	NR2F2	chr15:45323836-45324212	K562	blood:	n/a	n/a
31	POLR2A	chr15:45323831-45324132	HepG2	liver:	n/a	n/a
32	POLR2A	chr15:45323080-45323407	HepG2	liver:	n/a	n/a
33	POLR2A	chr15:45320182-45320473	HepG2	liver:	n/a	n/a
34	POLR2A	chr15:45321511-45321541	HepG2	liver:	n/a	n/a
35	POLR2A	chr15:45321952-45322182	HepG2	liver:	n/a	n/a
36	POLR2A	chr15:45321684-45321711	Hela-S3	cervix:	n/a	n/a
37	POLR2A	chr15:45323837-45324170	GM12891	blood:	n/a	n/a
38	POLR2A	chr15:45321702-45322091	GM12891	blood:	n/a	n/a
39	POLR2A	chr15:45320266-45320440	H1-hESC	embryonic stem cell:	n/a	n/a
40	POLR2A	chr15:45321728-45322278	SK-N-MC	brain:	n/a	n/a
41	POLR2A	chr15:45323930-45323966	MCF-7	breast:	n/a	n/a
42	POLR2A	chr15:45318942-45319169	HUVEC	blood vessel:	n/a	n/a
43	POLR2A	chr15:45321620-45321725	HepG2	liver:	n/a	n/a
44	POLR2A	chr15:45323694-45324119	K562	blood:	n/a	n/a
45	RCOR1	chr15:45319602-45319763	K562	blood:	n/a	n/a
46	RCOR1	chr15:45319522-45319779	K562	blood:	n/a	n/a
47	RCOR1	chr15:45323500-45323700	K562	blood:	n/a	n/a
48	RCOR1	chr15:45318877-45319103	K562	blood:	n/a	n/a
49	REST	chr15:45320263-45320445	H1-hESC	embryonic stem cell:	n/a	n/a
50	SETDB1	chr15:45321659-45322187	U2OS	brain:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:45319037-45319087	PANC-1	pancreas:	n/a
2	chr15:45319037-45319087	HCT-116	colon:	n/a
3	chr15:45319037-45319087	HCM	heart:	n/a
4	chr15:45319037-45319087	BJ	skin:	n/a
5	chr15:45319037-45319087	NH-A	brain:	n/a
6	chr15:45319037-45319087	SK-N-SH	brain:	n/a
7	chr15:45319037-45319087	GM19239	blood:	n/a
8	chr15:45319037-45319087	HNPCEpiC	eye:	n/a
9	chr15:45319037-45319087	AG04449	skin:	fetal
10	chr15:45319037-45319087	NHBE	bronchial:	n/a
11	chr15:45319037-45319087	PrEC	prostate:	n/a
12	chr15:45319037-45319087	HEK293	kidney:	embryo
13	chr15:45319037-45319087	HL-60	blood:	n/a
14	chr15:45319037-45319087	Jurkat	blood:	n/a
15	chr15:45319037-45319087	HepG2	liver:	n/a
16	chr15:45319037-45319087	ProgFib	skin:	n/a
17	chr15:45319037-45319087	Caco-2	colon:	n/a
18	chr15:45319037-45319087	IMR90	lung:	fetal
19	chr15:45319037-45319087	HUVEC	blood vessel:	n/a
20	chr15:45319037-45319087	HRPEpiC	eye:	n/a
21	chr15:45319037-45319087	AG10803	skin:	n/a
22	chr15:45319037-45319087	A549	lung:	n/a
23	chr15:45319037-45319087	Hepatocyte	liver:	n/a
24	chr15:45319037-45319087	SK-N-MC	brain:	n/a
25	chr15:45319037-45319087	H1-hESC	embryonic stem cell:	embryo
26	chr15:45319037-45319087	HCPEpiC	choroid plexus:	n/a
27	chr15:45319037-45319087	HRE	kidney:	n/a
28	chr15:45319037-45319087	SAEC	small airway:	n/a
29	chr15:45319037-45319087	HAEpiC	amniotic membrane:	n/a
30	chr15:45319037-45319087	ovcar-3	ovarian:	n/a
31	chr15:45319037-45319087	K562	blood:	n/a
32	chr15:45319037-45319087	Hela-S3	cervix:	n/a
33	chr15:45319037-45319087	NHDF-neo	bronchial:	n/a
34	chr15:45319037-45319087	HCF	heart:	n/a
35	chr15:45319037-45319087	GM12891	blood:	n/a
36	chr15:45319037-45319087	AoSMC	blood vessel:	n/a
37	chr15:45319037-45319087	BE2_C	brain:	n/a
38	chr15:45319037-45319087	LNCaP	prostate:	n/a
39	chr15:45319037-45319087	MCF10A-Er-Src	breast:	n/a
40	chr15:45319037-45319087	CMK	blood:	n/a
41	chr15:45319037-45319087	T-47D	breast:	n/a
42	chr15:45319037-45319087	SKMC	muscle:	n/a
43	chr15:45319037-45319087	GM12878	blood:	n/a
44	chr15:45319037-45319087	RPTEC	kidney:	n/a
45	chr15:45319037-45319087	U87	brain:	n/a
46	chr15:45319037-45319087	PFSK-1	brain:	n/a
47	chr15:45319037-45319087	HPAEpiC	pulmonary alveolar:	n/a
48	chr15:45319037-45319087	ECC-1	luminal epithelium:	n/a
49	chr15:45319037-45319087	GM12892	blood:	n/a
50	chr15:45319037-45319087	HEEpiC	esophagus:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:45313440..45317462-chr15:45317525..45323259,9	K562	blood:

No data

Variant related genes	Relation type
SORD	TF binding region
SORD	CpG island
ENSG00000140263	chromatin interactions

Extended variants
information (count: 349 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:349 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs563011198	chr15:45318841-45318842	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs148175784	chr15:45318860-45318861	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs150413781	chr15:45318886-45318887	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs79003388	chr15:45318891-45318892	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs141994651	chr15:45318898-45318899	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs562452317	chr15:45318903-45318904	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs527968425	chr15:45318939-45318940	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs76463192	chr15:45318950-45318951	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs80340448	chr15:45318965-45318966	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs115250682	chr15:45318975-45318976	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs72722055	chr15:45318980-45318981	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs188965571	chr15:45318986-45318987	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs72722056	chr15:45318996-45318997	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs533334428	chr15:45318998-45318999	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs550309568	chr15:45319006-45319007	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs79940886	chr15:45319016-45319017	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs74625019	chr15:45319038-45319039	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs570118301	chr15:45319057-45319058	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs191050623	chr15:45319058-45319059	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs35101733	chr15:45319072-45319073	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs398043229	chr15:45319073-45319074	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs555266236	chr15:45319088-45319089	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs75898226	chr15:45319092-45319093	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs373786579	chr15:45319098-45319099	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs13380326	chr15:45319111-45319112	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs529580823	chr15:45319117-45319118	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs74011304	chr15:45319118-45319119	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs534592429	chr15:45319119-45319120	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs66524218	chr15:45319138-45319139	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs559788143	chr15:45319140-45319141	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs558005631	chr15:45319144-45319145	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs386783575	chr15:45319145-45319146	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs78032427	chr15:45319181-45319182	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs371327533	chr15:45319188-45319189	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs386783576	chr15:45319193-45319194	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs145815326	chr15:45319195-45319196	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs386783577	chr15:45319203-45319204	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs56370055	chr15:45319206-45319207	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs530078569	chr15:45319231-45319232	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs77702836	chr15:45319242-45319243	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs77727319	chr15:45319246-45319247	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs75607614	chr15:45319249-45319250	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs548718941	chr15:45319264-45319265	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs367796510	chr15:45319281-45319282	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs542972603	chr15:45319304-45319305	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs74011305	chr15:45319307-45319308	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs77675005	chr15:45319322-45319323	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs573398545	chr15:45319323-45319324	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs78777288	chr15:45319329-45319330	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs112730365	chr15:45319348-45319349	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	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
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
Basal cell lymphoma	17053054	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
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Melanoma	17363583	CNVD
Acute myeloid leukemia	19651601	CNVD
Marfan syndrome	17492313	CNVD
Esophageal adenocarcinoma	18820669	CNVD

Chromatin state (count:308 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:45316000-45321600	Weak transcription	Aorta	Aorta
2	chr15:45316200-45326200	Weak transcription	Psoas Muscle	Psoas
3	chr15:45316200-45340600	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr15:45316400-45319200	Enhancers	Fetal Thymus	thymus
5	chr15:45316400-45320600	Weak transcription	Fetal Kidney	kidney
6	chr15:45316400-45321000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr15:45316400-45321400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr15:45316400-45321400	Weak transcription	Primary T cells from cord blood	blood
9	chr15:45316400-45321600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr15:45316400-45321600	Weak transcription	Right Atrium	heart
11	chr15:45316400-45321800	Weak transcription	Ovary	ovary
12	chr15:45316400-45323400	Weak transcription	Placenta Amnion	Placenta Amnion
13	chr15:45316400-45327600	Weak transcription	Primary B cells from cord blood	blood
14	chr15:45316400-45329400	Weak transcription	Primary T cells fromperipheralblood	blood
15	chr15:45316400-45333000	Weak transcription	Lung	lung
16	chr15:45316400-45341200	Weak transcription	Fetal Muscle Trunk	muscle
17	chr15:45316400-45342200	Weak transcription	HSMMtube	muscle
18	chr15:45316400-45342600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr15:45316600-45319000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr15:45316600-45319000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr15:45316600-45319000	Weak transcription	Duodenum Mucosa	Duodenum
22	chr15:45316600-45319000	Weak transcription	Left Ventricle	heart
23	chr15:45316600-45319000	Weak transcription	Right Ventricle	heart
24	chr15:45316600-45319400	Weak transcription	Brain Angular Gyrus	brain
25	chr15:45316600-45319400	Weak transcription	Brain Germinal Matrix	brain
26	chr15:45316600-45319800	Weak transcription	Pancreatic Islets	Pancreatic Islet
27	chr15:45316600-45321200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr15:45316600-45321400	Weak transcription	H9 Cell Line	embryonic stem cell
29	chr15:45316600-45321400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr15:45316600-45321400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr15:45316600-45321400	Weak transcription	Fetal Intestine Small	intestine
32	chr15:45316600-45321400	Weak transcription	Fetal Stomach	stomach
33	chr15:45316600-45321800	Weak transcription	Primary monocytes fromperipheralblood	blood
34	chr15:45316600-45322200	Weak transcription	Skeletal Muscle Male	skeletal muscle
35	chr15:45316600-45322800	Weak transcription	Colonic Mucosa	Colon
36	chr15:45316600-45323000	Weak transcription	H1 Cell Line	embryonic stem cell
37	chr15:45316600-45323000	Weak transcription	Fetal Muscle Leg	muscle
38	chr15:45316600-45324800	Weak transcription	Spleen	Spleen
39	chr15:45316600-45325400	Weak transcription	NHDF-Ad	bronchial
40	chr15:45316600-45326000	Weak transcription	Primary neutrophils fromperipheralblood	blood
41	chr15:45316600-45327000	Weak transcription	Esophagus	oesophagus
42	chr15:45316600-45328800	Weak transcription	Primary B cells from peripheral blood	blood
43	chr15:45316600-45328800	Weak transcription	Pancreas	Pancrea
44	chr15:45316600-45329000	Weak transcription	Rectal Mucosa Donor 31	rectum
45	chr15:45316600-45329000	Weak transcription	Stomach Smooth Muscle	stomach
46	chr15:45316600-45329000	Weak transcription	Osteobl	bone
47	chr15:45316600-45329200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
48	chr15:45316600-45329200	Weak transcription	NHLF	lung
49	chr15:45316600-45329400	Weak transcription	Rectal Smooth Muscle	rectum
50	chr15:45316600-45329600	Weak transcription	Rectal Mucosa Donor 29	rectum

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links