Variant report

Variant	nsv904289
Chromosome Location	chr15:62156690-62287456
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	chr15:62164156-62164420	K562	blood:	n/a	n/a
2	ARID3A	chr15:62180335-62180383	K562	blood:	n/a	n/a
3	ARID3A	chr15:62199453-62200154	HepG2	liver:	n/a	n/a
4	ARID3A	chr15:62164169-62164478	HepG2	liver:	n/a	n/a
5	ARID3A	chr15:62281922-62282216	K562	blood:	n/a	n/a
6	ARID3A	chr15:62171569-62171652	HepG2	liver:	n/a	n/a
7	BACH1	chr15:62281910-62282262	K562	blood:	n/a	n/a
8	BACH1	chr15:62281967-62282167	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr15:62234203-62234206	K562	blood:	n/a	n/a
10	BCL3	chr15:62255882-62256211	GM12878	blood:	n/a	n/a
11	BRCA1	chr15:62164191-62164533	Hela-S3	cervix:	n/a	n/a
12	CBX3	chr15:62185381-62185684	K562	blood:	n/a	n/a
13	CEBPB	chr15:62180280-62180649	IMR90	lung:	n/a	chr15:62180454-62180465
14	CEBPB	chr15:62266744-62266785	HepG2	liver:	n/a	n/a
15	CEBPB	chr15:62182374-62182601	A549	lung:	n/a	n/a
16	CEBPB	chr15:62199668-62200070	HepG2	liver:	n/a	n/a
17	CEBPB	chr15:62275283-62275661	Hela-S3	cervix:	n/a	chr15:62275465-62275476
18	CEBPB	chr15:62265786-62266041	A549	lung:	n/a	chr15:62265887-62265898 chr15:62265886-62265897 chr15:62265888-62265897
19	CEBPB	chr15:62180336-62180636	A549	lung:	n/a	chr15:62180454-62180465
20	CEBPB	chr15:62180357-62180498	H1-hESC	embryonic stem cell:	n/a	chr15:62180454-62180465
21	CEBPB	chr15:62180373-62180630	K562	blood:	n/a	chr15:62180454-62180465
22	CEBPB	chr15:62197996-62198309	HepG2	liver:	n/a	n/a
23	CEBPB	chr15:62265849-62266044	K562	blood:	n/a	chr15:62265887-62265898 chr15:62265886-62265897 chr15:62265888-62265897
24	CEBPB	chr15:62275362-62275602	HepG2	liver:	n/a	chr15:62275465-62275476
25	CEBPB	chr15:62171161-62171355	HepG2	liver:	n/a	chr15:62171168-62171181
26	CEBPB	chr15:62232985-62233209	HepG2	liver:	n/a	n/a
27	CEBPB	chr15:62275367-62275598	MCF-7	breast:	n/a	chr15:62275465-62275476
28	CEBPB	chr15:62180307-62180564	HepG2	liver:	n/a	chr15:62180454-62180465
29	CEBPB	chr15:62239060-62239292	IMR90	lung:	n/a	n/a
30	CEBPB	chr15:62227701-62228189	K562	blood:	n/a	chr15:62227893-62227904
31	CEBPB	chr15:62227747-62228056	Hela-S3	cervix:	n/a	chr15:62227893-62227904
32	CEBPB	chr15:62281886-62282169	K562	blood:	n/a	n/a
33	CEBPB	chr15:62275251-62275629	MCF-7	breast:	n/a	chr15:62275465-62275476
34	CEBPB	chr15:62180324-62180597	Hela-S3	cervix:	n/a	chr15:62180454-62180465
35	CEBPB	chr15:62265777-62266054	HepG2	liver:	n/a	chr15:62265887-62265898 chr15:62265886-62265897 chr15:62265888-62265897
36	CEBPB	chr15:62225483-62225689	K562	blood:	n/a	chr15:62225584-62225597 chr15:62225586-62225597 chr15:62225531-62225544 chr15:62225584-62225597 chr15:62225584-62225597 chr15:62225586-62225597
37	CEBPB	chr15:62227818-62228070	A549	lung:	n/a	chr15:62227893-62227904
38	CHD1	chr15:62163340-62163388	GM12878	blood:	n/a	n/a
39	CHD2	chr15:62221823-62221825	GM12878	blood:	n/a	n/a
40	CTCF	chr15:62164220-62164370	AG10803	skin:	n/a	chr15:62164293-62164314 chr15:62164291-62164309
41	CTCF	chr15:62164190-62164192	GM10266	blood:	n/a	n/a
42	CTCF	chr15:62164180-62164330	HepG2	liver:	n/a	chr15:62164293-62164314 chr15:62164291-62164309
43	CTCF	chr15:62164176-62164414	GM12878	blood:	n/a	chr15:62164293-62164314 chr15:62164291-62164309
44	CTCF	chr15:62164050-62164544	MCF-7	breast:	n/a	chr15:62164293-62164314 chr15:62164291-62164309
45	CTCF	chr15:62164171-62164388	LNCaP	prostate:	n/a	chr15:62164293-62164314 chr15:62164291-62164309
46	CTCF	chr15:62164220-62164370	GM12867	blood:	n/a	chr15:62164293-62164314 chr15:62164291-62164309
47	CTCF	chr15:62164180-62164330	HCT-116	colon:	n/a	chr15:62164293-62164314 chr15:62164291-62164309
48	CTCF	chr15:62201438-62201496	MCF-7	breast:	n/a	n/a
49	CTCF	chr15:62164220-62164370	HFF-Myc	foreskin:	n/a	chr15:62164293-62164314 chr15:62164291-62164309
50	CTCF	chr15:62164260-62164410	GM12866	blood:	n/a	chr15:62164293-62164314 chr15:62164291-62164309

No.	Distal block	Cell Line	Cell type
1	chr15:62170697..62173317-chr15:62182241..62184749,2	MCF-7	breast:
2	chr15:62204266..62207135-chr15:62210768..62213468,2	MCF-7	breast:
3	chr15:62223179..62225292-chr15:62226281..62228642,2	K562	blood:
4	chr11:22957855..22958444-chr15:62239142..62239729,2	MCF-7	breast:
5	chr15:62266682..62269656-chr15:62302600..62304271,2	K562	blood:
6	chr15:62157514..62159480-chr15:62215874..62217523,2	K562	blood:
7	chr15:62268988..62271189-chr15:62273485..62276457,2	MCF-7	breast:
8	chr15:62195135..62197262-chr15:62198825..62201096,2	MCF-7	breast:
9	chr15:62248426..62250802-chr15:62259693..62261364,2	K562	blood:
10	chr15:62236123..62237658-chr15:62241444..62244261,2	K562	blood:
11	chr15:62270934..62272587-chr15:62351243..62353224,2	MCF-7	breast:
12	chr15:62259986..62262200-chr15:62266004..62268197,2	K562	blood:
13	chr15:62213296..62215607-chr15:62227904..62230544,2	K562	blood:
14	chr15:62195135..62197262-chr15:62198825..62201096,2	MCF-7	breast:
15	chr15:62164230..62164773-chr15:62363602..62364393,2	K562	blood:
16	chr15:62242750..62243662-chr5:173738637..173739199,2	MCF-7	breast:
17	chr15:62280133..62283452-chr15:62316207..62318715,3	K562	blood:
18	chr15:62178968..62180848-chr15:62186299..62188013,2	K562	blood:
19	chr15:62268988..62271189-chr15:62273485..62276457,2	MCF-7	breast:
20	chr15:62178968..62180848-chr15:62186299..62188013,2	K562	blood:
21	chr15:62160043..62163025-chr15:62359293..62361455,2	MCF-7	breast:
22	chr15:62231542..62233712-chr15:62238622..62240411,2	K562	blood:
23	chr15:62235589..62237658-chr15:62241156..62242944,2	K562	blood:
24	chr15:62164211..62164737-chr15:62546261..62547255,2	K562	blood:
25	chr15:62222450..62224583-chr15:62247796..62249719,2	MCF-7	breast:
26	chr15:62241235..62242799-chr15:62250211..62252735,2	K562	blood:
27	chr15:62170697..62173317-chr15:62182241..62184749,2	MCF-7	breast:
28	chr15:62236123..62237658-chr15:62241444..62244261,2	K562	blood:
29	chr15:62275008..62277065-chr15:62352447..62354062,2	MCF-7	breast:
30	chr15:62252284..62254348-chr15:62257141..62258725,2	K562	blood:
31	chr15:62279274..62280986-chr15:62358759..62361498,2	MCF-7	breast:
32	chr15:62283890..62286224-chr15:62350363..62353063,2	K562	blood:
33	chr15:62148662..62150892-chr15:62154836..62157768,2	K562	blood:
34	chr15:62157514..62159480-chr15:62215874..62217523,2	K562	blood:
35	chr15:62205557..62210722-chr15:62211814..62216434,5	K562	blood:
36	chr15:62249551..62252071-chr15:62252647..62254754,2	MCF-7	breast:
37	chr15:62259986..62262200-chr15:62266004..62268197,2	K562	blood:
38	chr15:62241235..62242799-chr15:62250211..62252735,2	K562	blood:
39	chr15:62235589..62237658-chr15:62241156..62242944,2	K562	blood:
40	chr15:62223179..62225292-chr15:62226281..62228642,2	K562	blood:
41	chr15:62231542..62233712-chr15:62238622..62240411,2	K562	blood:
42	chr15:62213296..62215607-chr15:62227904..62230544,2	K562	blood:
43	chr15:62222450..62224583-chr15:62247796..62249719,2	MCF-7	breast:
44	chr15:62248426..62250802-chr15:62259693..62261364,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C2CD4A-10	chr15:62206624-62206875	NONHSAT044263

No.	miRNA target gene	miRNA name	Chromosome Location
1	VPS13C	hsa-miR-186-5p	chr15:62160021-62160015
2	VPS13C	hsa-miR-26b-5p	chr15:62160099-62160122
3	VPS13C	hsa-miR-186-5p	chr15:62160016-62160037
4	VPS13C	hsa-miR-26b-5p	chr15:62157423-62157416
5	VPS13C	hsa-miR-26b-5p	chr15:62160105-62160099
6	VPS13C	hsa-miR-128-3p	chr15:62160069-62160089

Variant related genes	Relation type
VPS13C	TF binding region
RN7SL613P	TF binding region
ENSG00000198535	chromatin interactions
ENSG00000264376	chromatin interactions
ENSG00000259251	chromatin interactions
ENSG00000129003	chromatin interactions

Extended variants
information (count: 5339 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:5339 , 50 per page) page: 1 2 3 4 5 6 7 ... 107

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3210522	chr15:62156690-62156691	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs150041472	chr15:62156717-62156718	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs551408040	chr15:62156801-62156802	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs144313255	chr15:62156804-62156805	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs537180209	chr15:62156815-62156816	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs562400430	chr15:62156865-62156866	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs555892848	chr15:62156878-62156879	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs191067149	chr15:62156898-62156899	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs183196552	chr15:62156918-62156919	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs535273025	chr15:62156926-62156927	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs553383768	chr15:62156980-62156981	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs578262720	chr15:62157010-62157011	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs11330878	chr15:62157077-62157078	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs545000791	chr15:62157093-62157094	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs186766271	chr15:62157132-62157133	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs575377706	chr15:62157134-62157135	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs148431822	chr15:62157147-62157148	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs8034185	chr15:62157151-62157152	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs78445252	chr15:62157157-62157158	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs189618717	chr15:62157188-62157189	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs565029705	chr15:62157304-62157305	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs532300017	chr15:62157343-62157344	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs4775446	chr15:62157366-62157367	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs539167131	chr15:62157382-62157383	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs537118522	chr15:62157392-62157393	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs370210005	chr15:62157393-62157394	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs115167563	chr15:62157412-62157413	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs142585379	chr15:62157459-62157460	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs17303866	chr15:62157461-62157462	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs571956992	chr15:62157488-62157489	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs539358841	chr15:62157503-62157504	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs556969575	chr15:62157527-62157528	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs8037603	chr15:62157537-62157538	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs182731488	chr15:62157553-62157554	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs554359397	chr15:62157569-62157570	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs17303873	chr15:62157573-62157574	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs12915283	chr15:62157579-62157580	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs576563872	chr15:62157582-62157583	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs188053714	chr15:62157635-62157636	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs532239185	chr15:62157666-62157667	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs544119292	chr15:62157677-62157678	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs71411466	chr15:62157709-62157710	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs563295014	chr15:62157738-62157739	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs530821138	chr15:62157752-62157753	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs147588281	chr15:62157759-62157760	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs553736933	chr15:62157762-62157763	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs141989687	chr15:62157769-62157770	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs201892206	chr15:62157786-62157787	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs117905423	chr15:62157795-62157796	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs577937629	chr15:62157802-62157803	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

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
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
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21341218	CNVD
Holoprosencephaly	21359414	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Mental retardation	17124404	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Renal cell carcinoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Melanoma	20877625	CNVD
Ovarian cancer	21781307	CNVD

Chromatin state (count:2853 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:62132400-62159000	Weak transcription	HSMM	muscle
2	chr15:62132400-62171200	Weak transcription	HMEC	breast
3	chr15:62135000-62161600	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr15:62138800-62184200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr15:62139200-62182200	Weak transcription	Brain Substantia Nigra	brain
6	chr15:62139800-62185200	Weak transcription	NHLF	lung
7	chr15:62140000-62184800	Weak transcription	Right Ventricle	heart
8	chr15:62140200-62180000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr15:62141200-62165400	Weak transcription	Brain Hippocampus Middle	brain
10	chr15:62141400-62160600	Weak transcription	Placenta	Placenta
11	chr15:62141400-62161400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr15:62141600-62161400	Weak transcription	Sigmoid Colon	Sigmoid Colon
13	chr15:62141600-62165000	Weak transcription	Thymus	Thymus
14	chr15:62142000-62165000	Weak transcription	Gastric	stomach
15	chr15:62142000-62209400	Weak transcription	Colonic Mucosa	Colon
16	chr15:62142200-62161600	Weak transcription	Fetal Stomach	stomach
17	chr15:62142200-62162800	Weak transcription	Hela-S3	cervix
18	chr15:62142400-62160800	Weak transcription	Fetal Muscle Trunk	muscle
19	chr15:62142400-62163800	Weak transcription	Brain Inferior Temporal Lobe	brain
20	chr15:62142400-62253000	Weak transcription	Spleen	Spleen
21	chr15:62142600-62209200	Weak transcription	K562	blood
22	chr15:62143000-62164000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr15:62143800-62182200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr15:62143800-62235600	Weak transcription	Fetal Brain Male	brain
25	chr15:62144000-62159800	Weak transcription	Osteobl	bone
26	chr15:62144000-62194600	Weak transcription	Fetal Lung	lung
27	chr15:62144200-62160600	Weak transcription	Fetal Thymus	thymus
28	chr15:62144800-62161400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
29	chr15:62144800-62162400	Weak transcription	Rectal Smooth Muscle	rectum
30	chr15:62144800-62184000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr15:62145200-62160600	Weak transcription	Skeletal Muscle Male	skeletal muscle
32	chr15:62145200-62163400	Weak transcription	Brain Cingulate Gyrus	brain
33	chr15:62145200-62182000	Weak transcription	NHEK	skin
34	chr15:62145400-62171600	Weak transcription	Stomach Mucosa	stomach
35	chr15:62145800-62182000	Weak transcription	Small Intestine	intestine
36	chr15:62146800-62230000	Weak transcription	Pancreas	Pancrea
37	chr15:62147000-62161800	Weak transcription	NHDF-Ad	bronchial
38	chr15:62147000-62162800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr15:62147000-62181800	Weak transcription	Brain Anterior Caudate	brain
40	chr15:62147000-62184000	Weak transcription	Lung	lung
41	chr15:62147200-62158400	Weak transcription	Rectal Mucosa Donor 31	rectum
42	chr15:62147200-62160800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr15:62147200-62161400	Weak transcription	Fetal Muscle Leg	muscle
44	chr15:62147200-62164600	Weak transcription	Cortex derived primary cultured neurospheres	brain
45	chr15:62147200-62165200	Weak transcription	Colon Smooth Muscle	Colon
46	chr15:62147400-62162600	Weak transcription	Stomach Smooth Muscle	stomach
47	chr15:62147600-62161400	Weak transcription	Skeletal Muscle Female	skeletal muscle
48	chr15:62147800-62160600	Weak transcription	Duodenum Smooth Muscle	Duodenum
49	chr15:62147800-62162400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr15:62147800-62184000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain

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