Variant report

Variant	nsv1055119
Chromosome Location	chr15:50861470-50900685
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:169)
CpG islands
(count:0)
Chromatin interactive
region (count:41)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:169 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:50888476-50888556	K562	blood:	n/a	n/a
2	ARID3A	chr15:50885990-50886949	K562	blood:	n/a	n/a
3	ATF1	chr15:50886574-50886849	K562	blood:	n/a	n/a
4	BACH1	chr15:50869823-50869907	K562	blood:	n/a	n/a
5	BACH1	chr15:50869845-50869896	H1-hESC	embryonic stem cell:	n/a	n/a
6	CCNT2	chr15:50886474-50886898	K562	blood:	n/a	n/a
7	CEBPB	chr15:50879839-50880023	HepG2	liver:	n/a	chr15:50879905-50879916
8	CEBPB	chr15:50880400-50880451	A549	lung:	n/a	n/a
9	CEBPB	chr15:50861954-50862152	A549	lung:	n/a	n/a
10	CEBPB	chr15:50889075-50889077	K562	blood:	n/a	n/a
11	CEBPB	chr15:50880374-50880513	K562	blood:	n/a	chr15:50880463-50880474
12	CEBPB	chr15:50886533-50886784	K562	blood:	n/a	n/a
13	CEBPB	chr15:50874149-50874329	HepG2	liver:	n/a	chr15:50874215-50874226
14	CEBPB	chr15:50879756-50879976	A549	lung:	n/a	chr15:50879905-50879916
15	CEBPB	chr15:50881597-50881743	IMR90	lung:	n/a	n/a
16	CEBPB	chr15:50894818-50895097	HepG2	liver:	n/a	n/a
17	CEBPB	chr15:50894829-50895045	A549	lung:	n/a	n/a
18	CEBPB	chr15:50881732-50881885	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr15:50889065-50889265	IMR90	lung:	n/a	n/a
20	CEBPB	chr15:50881475-50881754	K562	blood:	n/a	chr15:50881581-50881594 chr15:50881581-50881594
21	CEBPD	chr15:50886419-50886927	K562	blood:	n/a	n/a
22	CEBPD	chr15:50886481-50887012	K562	blood:	n/a	n/a
23	CTCF	chr15:50886367-50886634	K562	blood:	n/a	n/a
24	CUX1	chr15:50886082-50886893	K562	blood:	n/a	n/a
25	EP300	chr15:50886594-50886920	K562	blood:	n/a	n/a
26	EP300	chr15:50885694-50886922	K562	blood:	n/a	chr15:50886576-50886590 chr15:50886105-50886119 chr15:50886401-50886415 chr15:50886171-50886180 chr15:50886152-50886161
27	FAM48A	chr15:50861712-50862060	GM12878	blood:	n/a	n/a
28	FAM48A	chr15:50889459-50889709	Hela-S3	cervix:	n/a	n/a
29	FOS	chr15:50870560-50870793	MCF10A-Er-Src	breast:	n/a	n/a
30	FOS	chr15:50889093-50889293	MCF10A-Er-Src	breast:	n/a	n/a
31	FOS	chr15:50889204-50889279	MCF10A-Er-Src	breast:	n/a	n/a
32	GABPA	chr15:50886560-50886826	K562	blood:	n/a	n/a
33	GATA1	chr15:50885751-50887419	K562	blood:	n/a	n/a
34	GATA1	chr15:50886445-50886849	PBDEFetal	blood:	n/a	n/a
35	GATA1	chr15:50885889-50887348	PBDE	blood:	n/a	n/a
36	GATA2	chr15:50886465-50886845	K562	blood:	n/a	n/a
37	GATA2	chr15:50886486-50886801	K562	blood:	n/a	n/a
38	GATA3	chr15:50890934-50891109	SH-SY5Y	brain:	n/a	n/a
39	GATA3	chr15:50900502-50901256	MCF-7	breast:	n/a	n/a
40	GATA3	chr15:50882587-50882843	T-47D	breast:	n/a	n/a
41	GATA3	chr15:50882540-50882795	MCF-7	breast:	n/a	n/a
42	HMGN3	chr15:50886582-50886805	K562	blood:	n/a	n/a
43	IRF1	chr15:50885713-50886885	K562	blood:	n/a	chr15:50886104-50886118 chr15:50886167-50886184 chr15:50886163-50886183
44	IRF1	chr15:50886003-50886256	K562	blood:	n/a	chr15:50886104-50886118 chr15:50886167-50886184 chr15:50886163-50886183
45	IRF1	chr15:50886551-50886953	K562	blood:	n/a	n/a
46	JUN	chr15:50886078-50886848	K562	blood:	n/a	chr15:50886169-50886178
47	JUND	chr15:50886520-50886889	K562	blood:	n/a	n/a
48	KAP1	chr15:50886327-50886612	K562	blood:	n/a	n/a
49	MAFF	chr15:50899359-50899660	HepG2	liver:	n/a	n/a
50	MAFF	chr15:50869825-50870034	K562	blood:	n/a	chr15:50869881-50869899

No data

(count:41 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:50646568..50648510-chr15:50882199..50884053,2	MCF-7	breast:
2	chr15:50866589..50868103-chr15:50868342..50870495,2	K562	blood:
3	chr15:50646177..50648161-chr15:50884558..50887057,2	K562	blood:
4	chr15:50872361..50874007-chr15:50875166..50877011,2	K562	blood:
5	chr15:50867388..50869846-chr15:50878063..50879633,2	MCF-7	breast:
6	chr15:50889435..50893254-chr15:50893944..50897716,3	K562	blood:
7	chr15:50646822..50648460-chr15:50870305..50871829,2	MCF-7	breast:
8	chr15:50872361..50874007-chr15:50875166..50877011,2	K562	blood:
9	chr15:50897808..50900573-chr15:50902086..50904020,3	K562	blood:
10	chr15:50646616..50649528-chr15:50876208..50878144,2	MCF-7	breast:
11	chr15:50871076..50873819-chr15:50876627..50878202,2	MCF-7	breast:
12	chr15:50878762..50881023-chr15:50884773..50886938,2	K562	blood:
13	chr15:50855242..50858331-chr15:50858835..50863040,3	MCF-7	breast:
14	chr15:50889745..50892079-chr19:13048030..13049882,2	MCF-7	breast:
15	chr15:50882354..50884324-chr15:50884736..50886650,2	MCF-7	breast:
16	chr15:50885676..50889608-chr15:50891608..50893462,3	K562	blood:
17	chr15:50872498..50875116-chr15:50878753..50881368,3	K562	blood:
18	chr15:50882354..50884324-chr15:50884736..50886650,2	MCF-7	breast:
19	chr15:50871076..50873819-chr15:50876627..50878202,2	MCF-7	breast:
20	chr15:50890587..50894134-chr15:50900500..50903052,3	MCF-7	breast:
21	chr15:50646359..50649336-chr15:50872616..50874692,3	MCF-7	breast:
22	chr15:50645917..50650602-chr15:50893213..50896172,4	MCF-7	breast:
23	chr15:50872498..50875116-chr15:50878753..50881368,3	K562	blood:
24	chr15:50859308..50861522-chr15:50879370..50881097,2	K562	blood:
25	chr15:50864188..50868322-chr15:50872346..50875460,4	MCF-7	breast:
26	chr15:50872361..50874197-chr15:50874784..50877011,2	K562	blood:
27	chr15:50861509..50865180-chr15:50865318..50870216,6	K562	blood:
28	chr15:50894679..50897378-chr15:50902879..50904659,2	MCF-7	breast:
29	chr15:50869972..50871677-chr15:51057056..51058734,2	MCF-7	breast:
30	chr15:50859308..50861522-chr15:50879370..50881097,2	K562	blood:
31	chr15:50864188..50868322-chr15:50872346..50875460,4	MCF-7	breast:
32	chr15:50885914..50887497-chr15:50920391..50922756,2	K562	blood:
33	chr15:50865776..50869008-chr15:50882396..50886787,3	K562	blood:
34	chr15:50869586..50872138-chr15:50874488..50876598,3	K562	blood:
35	chr15:50647415..50649249-chr15:50862816..50866408,3	MCF-7	breast:
36	chr15:50881070..50883291-chr15:50976406..50979005,2	MCF-7	breast:
37	chr15:50865607..50867294-chr15:50870808..50872374,2	K562	blood:
38	chr15:50872361..50874197-chr15:50874784..50877011,2	K562	blood:
39	chr15:50551676..50553333-chr15:50885793..50888407,2	K562	blood:
40	chr15:50865794..50868217-chr15:50870874..50873456,2	K562	blood:
41	chr15:50646177..50649955-chr15:50884558..50888661,4	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-USP50-5	chr15:50879699-50880406	l_1156_chr15:50879698-50884434_liver
2	lnc-USP50-5	chr15:50883698-50883786	l_1156_chr15:50879698-50884434_liver
3	lnc-USP8-3	chr15:50873840-50874894	l_1155_chr15:50872073-50874894_testes
4	lnc-USP8-3	chr15:50872074-50872178	l_1155_chr15:50872073-50874894_testes
5	lnc-USP50-5	chr15:50882478-50883336	l_1156_chr15:50879698-50884434_liver
6	lnc-USP50-5	chr15:50883983-50884434	l_1156_chr15:50879698-50884434_liver

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	TRPM7	hsa-miR-10a-5p	chr15:50896505-50896530
2	TRPM7	hsa-miR-10a-5p	chr15:50896593-50896615

Variant related genes	Relation type
TRPM7	TF binding region
ENSG00000244879	chromatin interactions
ENSG00000092439	chromatin interactions
ENSG00000104064	chromatin interactions
ENSG00000138600	chromatin interactions
ENSG00000179218	chromatin interactions

Extended variants
information (count: 1622 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:1622 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3131578	chr15:50861470-50861471	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs143994851	chr15:50861530-50861531	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs570739485	chr15:50861556-50861557	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs75273645	chr15:50861558-50861559	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs545957853	chr15:50861586-50861587	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs540407862	chr15:50861606-50861607	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs553385676	chr15:50861622-50861623	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs146864686	chr15:50861666-50861667	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs562000605	chr15:50861681-50861682	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs372260887	chr15:50861724-50861725	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs149006435	chr15:50861775-50861776	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs529171966	chr15:50861843-50861844	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs557134231	chr15:50861870-50861871	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs574964948	chr15:50861880-50861881	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs143841062	chr15:50861895-50861896	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs557870363	chr15:50861897-50861898	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs376280555	chr15:50861929-50861930	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs370442170	chr15:50861936-50861937	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs148136101	chr15:50861946-50861947	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs540270954	chr15:50862015-50862016	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs141059486	chr15:50862026-50862027	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs146476441	chr15:50862028-50862029	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs114188943	chr15:50862043-50862044	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs139150271	chr15:50862044-50862045	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs373590475	chr15:50862065-50862066	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs199864645	chr15:50862118-50862119	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs184526596	chr15:50862148-50862149	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs373422442	chr15:50862182-50862183	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs192362109	chr15:50862209-50862210	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs370242772	chr15:50862214-50862215	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs570970677	chr15:50862218-50862219	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs528465556	chr15:50862221-50862222	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs373487160	chr15:50862222-50862223	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs546981420	chr15:50862227-50862228	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs183923083	chr15:50862229-50862230	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs189359502	chr15:50862231-50862232	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs377443311	chr15:50862238-50862239	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs535766719	chr15:50862246-50862247	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs532930096	chr15:50862247-50862248	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs201159511	chr15:50862297-50862298	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs55722054	chr15:50862303-50862304	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs117899712	chr15:50862357-50862358	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs557565820	chr15:50862363-50862364	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs12914001	chr15:50862376-50862377	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs572937051	chr15:50862393-50862394	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs533515231	chr15:50862440-50862441	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs79561148	chr15:50862460-50862461	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs555348530	chr15:50862462-50862463	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs573957995	chr15:50862577-50862578	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs528803198	chr15:50862636-50862637	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	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
Myelofibrosis	22110671	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	21364760	CNVD
Bipolar disorder	19114987	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Pancreatic cancer	17952125	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1083 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:50837000-50862200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr15:50837000-50882800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr15:50844200-50862200	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr15:50846000-50950800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr15:50846200-50867000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr15:50847000-50920600	Weak transcription	Aorta	Aorta
7	chr15:50847600-50865200	Weak transcription	Rectal Smooth Muscle	rectum
8	chr15:50847600-50866400	Weak transcription	Placenta Amnion	Placenta Amnion
9	chr15:50847800-50872200	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr15:50848000-50868200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr15:50848400-50864800	Weak transcription	Brain Hippocampus Middle	brain
12	chr15:50848800-50894800	Strong transcription	Liver	Liver
13	chr15:50849000-50868800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
14	chr15:50849000-50894600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr15:50849200-50864200	Weak transcription	Colonic Mucosa	Colon
16	chr15:50849200-50869000	Weak transcription	Esophagus	oesophagus
17	chr15:50849200-50874400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
18	chr15:50849200-50883600	Weak transcription	Pancreas	Pancrea
19	chr15:50849200-50883600	Weak transcription	Small Intestine	intestine
20	chr15:50849400-50869000	Weak transcription	Gastric	stomach
21	chr15:50849600-50863400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
22	chr15:50849600-50864000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
23	chr15:50849600-50866000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
24	chr15:50849600-50871800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr15:50849800-50862400	Strong transcription	Primary monocytes fromperipheralblood	blood
26	chr15:50849800-50872800	Strong transcription	Fetal Intestine Large	intestine
27	chr15:50850000-50864800	Weak transcription	Colon Smooth Muscle	Colon
28	chr15:50850000-50865400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
29	chr15:50850200-50870600	Strong transcription	Muscle Satellite Cultured Cells	--
30	chr15:50850400-50870400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr15:50850600-50865200	Weak transcription	Brain Substantia Nigra	brain
32	chr15:50850600-50872800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr15:50850800-50892000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr15:50851000-50864200	Weak transcription	Fetal Kidney	kidney
35	chr15:50851400-50862600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr15:50851600-50862600	Strong transcription	Monocytes-CD14+_RO01746	blood
37	chr15:50851800-50936400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
38	chr15:50852000-50897400	Strong transcription	HUES64 Cell Line	embryonic stem cell
39	chr15:50852200-50864000	Weak transcription	Brain Cingulate Gyrus	brain
40	chr15:50852200-50890200	Weak transcription	Psoas Muscle	Psoas
41	chr15:50852200-50896800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr15:50852600-50866400	Weak transcription	Brain Germinal Matrix	brain
43	chr15:50852800-50862000	Strong transcription	Hela-S3	cervix
44	chr15:50852800-50879000	Strong transcription	Adipose Nuclei	Adipose
45	chr15:50852800-50887200	Strong transcription	Rectal Mucosa Donor 29	rectum
46	chr15:50852800-50888600	Strong transcription	HUES48 Cell Line	embryonic stem cell
47	chr15:50852800-50893200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr15:50853000-50872600	Strong transcription	Fetal Thymus	thymus
49	chr15:50853000-50872800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
50	chr15:50853400-50867000	Weak transcription	Brain Angular Gyrus	brain

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