Variant report

Variant	nsv466723
Chromosome Location	chr10:5920836-5930579
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:73)
CpG islands
(count:61)
Chromatin interactive
region (count:22)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:73 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:5930437-5930734	HepG2	liver:	n/a	n/a
2	BHLHE40	chr10:5930389-5931229	HepG2	liver:	n/a	n/a
3	CEBPB	chr10:5930354-5930729	HepG2	liver:	n/a	n/a
4	CEBPB	chr10:5930361-5930730	HepG2	liver:	n/a	n/a
5	CEBPB	chr10:5930358-5930749	IMR90	lung:	n/a	chr10:5930719-5930731
6	CEBPB	chr10:5928985-5929332	IMR90	lung:	n/a	n/a
7	CEBPB	chr10:5930400-5930637	HepG2	liver:	n/a	n/a
8	CEBPB	chr10:5930378-5930839	K562	blood:	n/a	chr10:5930719-5930731
9	CTCF	chr10:5927633-5927774	LNCaP	prostate:	n/a	n/a
10	CTCF	chr10:5927628-5927818	LNCaP	prostate:	n/a	n/a
11	CTCF	chr10:5927596-5927883	GM12878	blood:	n/a	n/a
12	CTCF	chr10:5927660-5927810	MCF-7	breast:	n/a	n/a
13	CTCF	chr10:5927665-5927789	MCF-7	breast:	n/a	n/a
14	CTCF	chr10:5930375-5930491	GM12878	blood:	n/a	chr10:5930437-5930444
15	CTCF	chr10:5927620-5927770	Caco-2	colon:	n/a	n/a
16	CUX1	chr10:5926967-5926971	K562	blood:	n/a	n/a
17	EP300	chr10:5930318-5930672	HepG2	liver:	n/a	n/a
18	FOS	chr10:5930542-5930710	MCF10A-Er-Src	breast:	n/a	n/a
19	FOS	chr10:5930478-5930672	MCF10A-Er-Src	breast:	n/a	n/a
20	FOXA1	chr10:5927705-5928081	T-47D	breast:	n/a	chr10:5927926-5927941
21	HEY1	chr10:5930328-5930725	HepG2	liver:	n/a	n/a
22	HEY1	chr10:5930487-5930793	HepG2	liver:	n/a	n/a
23	JUN	chr10:5930416-5930736	HepG2	liver:	n/a	n/a
24	JUND	chr10:5930405-5930706	HepG2	liver:	n/a	n/a
25	MAFF	chr10:5922732-5922820	K562	blood:	n/a	n/a
26	MAX	chr10:5930413-5930626	HepG2	liver:	n/a	n/a
27	MAX	chr10:5930268-5932989	HepG2	liver:	n/a	chr10:5932340-5932350
28	MAX	chr10:5930403-5932406	MCF-7	breast:	n/a	chr10:5932340-5932350
29	MAX	chr10:5930399-5933314	K562	blood:	n/a	chr10:5932340-5932350
30	MAX	chr10:5930370-5932966	HepG2	liver:	n/a	chr10:5932340-5932350
31	MAZ	chr10:5930138-5933189	IMR90	lung:	n/a	chr10:5932340-5932350
32	MTA3	chr10:5930118-5931295	GM12878	blood:	n/a	n/a
33	MXI1	chr10:5928892-5928910	GM12878	blood:	n/a	n/a
34	MXI1	chr10:5930179-5932450	IMR90	lung:	n/a	n/a
35	MXI1	chr10:5930417-5932848	HepG2	liver:	n/a	n/a
36	MXI1	chr10:5929938-5933656	SK-N-SH	brain:	n/a	n/a
37	MYBL2	chr10:5930200-5930813	HepG2	liver:	n/a	n/a
38	MYC	chr10:5930413-5930731	MCF10A-Er-Src	breast:	n/a	n/a
39	MYC	chr10:5930354-5930752	MCF10A-Er-Src	breast:	n/a	n/a
40	MYC	chr10:5930472-5930587	HepG2	liver:	n/a	n/a
41	PAX5	chr10:5930373-5930708	GM12878	blood:	n/a	n/a
42	POLR2A	chr10:5930524-5930544	K562	blood:	n/a	n/a
43	POLR2A	chr10:5930488-5931295	HepG2	liver:	n/a	n/a
44	POLR2A	chr10:5930492-5931178	MCF10A-Er-Src	breast:	n/a	n/a
45	POLR2A	chr10:5926137-5926159	HepG2	liver:	n/a	n/a
46	POLR2A	chr10:5926015-5926037	HepG2	liver:	n/a	n/a
47	POLR2A	chr10:5927978-5927982	HepG2	liver:	n/a	n/a
48	POLR2A	chr10:5930268-5931214	HepG2	liver:	n/a	n/a
49	POLR2A	chr10:5930342-5930771	HepG2	liver:	n/a	n/a
50	POLR2A	chr10:5929530-5929637	H1-hESC	embryonic stem cell:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:5930543-5930593	SK-N-MC	brain:	n/a
2	chr10:5930543-5930593	SKMC	muscle:	n/a
3	chr10:5930543-5930593	U87	brain:	n/a
4	chr10:5930543-5930593	NB4	blood:	n/a
5	chr10:5930543-5930593	PrEC	prostate:	n/a
6	chr10:5930543-5930593	HAEpiC	amniotic membrane:	n/a
7	chr10:5930543-5930593	GM12891	blood:	n/a
8	chr10:5930543-5930593	HUVEC	blood vessel:	n/a
9	chr10:5930543-5930593	HEK293	kidney:	embryo
10	chr10:5930543-5930593	HRCEpiC	kidney:	n/a
11	chr10:5930543-5930593	SAEC	small airway:	n/a
12	chr10:5930543-5930593	RPTEC	kidney:	n/a
13	chr10:5930543-5930593	MCF-7	breast:	n/a
14	chr10:5930543-5930593	GM19239	blood:	n/a
15	chr10:5930543-5930593	ovcar-3	ovarian:	n/a
16	chr10:5930543-5930593	HepG2	liver:	n/a
17	chr10:5930543-5930593	HPAEpiC	pulmonary alveolar:	n/a
18	chr10:5930543-5930593	HMEC	breast:	n/a
19	chr10:5930543-5930593	NHBE	bronchial:	n/a
20	chr10:5930543-5930593	Hela-S3	cervix:	n/a
21	chr10:5930543-5930593	ProgFib	skin:	n/a
22	chr10:5930543-5930593	HRPEpiC	eye:	n/a
23	chr10:5930543-5930593	Caco-2	colon:	n/a
24	chr10:5930543-5930593	PFSK-1	brain:	n/a
25	chr10:5930543-5930593	Hepatocyte	liver:	n/a
26	chr10:5930543-5930593	PANC-1	pancreas:	n/a
27	chr10:5930543-5930593	HEEpiC	esophagus:	n/a
28	chr10:5930543-5930593	SK-N-SH	brain:	n/a
29	chr10:5930543-5930593	H1-hESC	embryonic stem cell:	embryo
30	chr10:5930543-5930593	IMR90	lung:	fetal
31	chr10:5930543-5930593	HNPCEpiC	eye:	n/a
32	chr10:5930543-5930593	BE2_C	brain:	n/a
33	chr10:5930543-5930593	NH-A	brain:	n/a
34	chr10:5930543-5930593	HCT-116	colon:	n/a
35	chr10:5930543-5930593	GM12892	blood:	n/a
36	chr10:5930543-5930593	SK-N-SH_RA	brain:	n/a
37	chr10:5930543-5930593	ECC-1	luminal epithelium:	n/a
38	chr10:5930543-5930593	HL-60	blood:	n/a
39	chr10:5930543-5930593	AG09309	skin:	n/a
40	chr10:5930543-5930593	GM06990	blood:	n/a
41	chr10:5930543-5930593	HCM	heart:	n/a
42	chr10:5930543-5930593	AG04450	lung:	fetal
43	chr10:5930543-5930593	Jurkat	blood:	n/a
44	chr10:5930543-5930593	AG09319	gingival:	n/a
45	chr10:5930543-5930593	HIPEpiC	eye:	n/a
46	chr10:5930543-5930593	AG10803	skin:	n/a
47	chr10:5930543-5930593	BJ	skin:	n/a
48	chr10:5930543-5930593	GM12878	blood:	n/a
49	chr10:5930543-5930593	AG04449	skin:	fetal
50	chr10:5930543-5930593	NT2-D1	testis:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:5853820..5856785-chr10:5927225..5934067,15	K562	blood:
2	chr10:5488345..5491486-chr10:5930515..5933192,3	MCF-7	breast:
3	chr10:5912116..5916503-chr10:5917203..5921455,4	K562	blood:
4	chr10:5904346..5907644-chr10:5928919..5931742,3	MCF-7	breast:
5	chr10:5917302..5921893-chr10:5926757..5932751,9	MCF-7	breast:
6	chr10:5854140..5855797-chr10:5921600..5924146,3	MCF-7	breast:
7	chr10:5912111..5919800-chr10:5923492..5927477,10	MCF-7	breast:
8	chr10:5853532..5857435-chr10:5928623..5934190,13	MCF-7	breast:
9	chr10:5930440..5932910-chr10:5957697..5960803,4	MCF-7	breast:
10	chr10:5487428..5490413-chr10:5923426..5925612,2	MCF-7	breast:
11	chr10:5914288..5916815-chr10:5925333..5927218,2	MCF-7	breast:
12	chr10:5919010..5920872-chr10:5921692..5924189,2	K562	blood:
13	chr10:5725094..5729377-chr10:5927689..5933777,6	MCF-7	breast:
14	chr10:5913737..5922370-chr10:5922961..5932189,19	K562	blood:
15	chr10:5919010..5920872-chr10:5921692..5924189,2	K562	blood:
16	chr10:5918577..5924576-chr10:5927726..5932597,9	MCF-7	breast:
17	chr10:5852595..5861125-chr10:5921136..5936216,31	MCF-7	breast:
18	chr10:5915609..5918597-chr10:5924591..5926431,2	K562	blood:
19	chr10:5853439..5857708-chr10:5926443..5936823,24	K562	blood:
20	chr10:5929157..5931311-chr10:6018059..6019673,2	MCF-7	breast:
21	chr10:5930398..5933295-chr10:6184026..6187985,3	K562	blood:
22	chr10:5925580..5929335-chr10:5933926..5939138,5	K562	blood:

No data

Variant related genes	Relation type
ANKRD16	TF binding region
FBXO18	TF binding region
ANKRD16	CpG island
FBXO18	CpG island
ENSG00000170525	chromatin interactions
ENSG00000240180	chromatin interactions
ENSG00000108021	chromatin interactions
ENSG00000173848	chromatin interactions
ENSG00000057608	chromatin interactions
ENSG00000272764	chromatin interactions
ENSG00000134470	chromatin interactions
ENSG00000134461	chromatin interactions
ENSG00000134452	chromatin interactions

Extended variants
information (count: 495 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:495 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2985044	chr10:5920836-5920837	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs536792215	chr10:5920849-5920850	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs557684049	chr10:5920882-5920883	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs11255698	chr10:5920893-5920894	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs142646923	chr10:5920923-5920924	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs187841555	chr10:5920936-5920937	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs151010174	chr10:5920941-5920942	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs9424023	chr10:5920977-5920978	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs59245904	chr10:5921025-5921026	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs610335	chr10:5921043-5921044	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs192797717	chr10:5921054-5921055	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs575650450	chr10:5921087-5921088	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs545903619	chr10:5921124-5921125	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs564106450	chr10:5921162-5921163	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs528490427	chr10:5921187-5921188	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs140827224	chr10:5921221-5921222	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs544793973	chr10:5921240-5921241	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs150151055	chr10:5921270-5921271	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs529983152	chr10:5921275-5921276	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs56977736	chr10:5921314-5921315	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs583630	chr10:5921358-5921359	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs622488	chr10:5921362-5921363	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs584000	chr10:5921395-5921396	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs12763478	chr10:5921399-5921400	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs79091828	chr10:5921432-5921433	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs77026709	chr10:5921446-5921447	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs552315237	chr10:5921476-5921477	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs138992668	chr10:5921513-5921514	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs35007091	chr10:5921520-5921521	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs117198509	chr10:5921532-5921533	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs552735618	chr10:5921534-5921535	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs1707228	chr10:5921537-5921538	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs113025962	chr10:5921603-5921604	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs557489258	chr10:5921606-5921607	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs184899864	chr10:5921639-5921640	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs545865190	chr10:5921679-5921680	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs60261178	chr10:5921682-5921683	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs77345026	chr10:5921683-5921684	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs200052859	chr10:5921684-5921685	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs140740896	chr10:5921686-5921687	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs372936999	chr10:5921687-5921688	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs59083212	chr10:5921688-5921689	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs151321997	chr10:5921690-5921691	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs34736787	chr10:5921691-5921692	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs374903450	chr10:5921699-5921700	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs557810448	chr10:5921720-5921721	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs573033895	chr10:5921723-5921724	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs375836951	chr10:5921752-5921753	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs370124505	chr10:5921753-5921754	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs373018035	chr10:5921755-5921756	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Sudden cardiac death	19188705	CNVD
Digeorge syndrome	22283845	CNVD
Cancer	21129771	CNVD
Colorectal cancer	20709793	CNVD
Wilms tumour	19047088	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Barakat syndrome	22470819	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	21720365	CNVD
Autism	18414403	CNVD
Malignant melanoma	18718029	CNVD
Breast cancer	22032731	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Phyllodes tumor	17334353	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Breast cancer	21785460	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Renal cell carcinoma	18765545	CNVD
lymphocytic leukemia	21291569	CNVD
Urothelial cell carcinoma	18451213	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Ovarian cancer	22355333	CNVD
Breast cancer	22522925	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:654 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:5903400-5925000	Weak transcription	Fetal Kidney	kidney
2	chr10:5909600-5924800	Weak transcription	Stomach Mucosa	stomach
3	chr10:5911600-5926800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr10:5913000-5929800	Weak transcription	Fetal Heart	heart
5	chr10:5913000-5929800	Weak transcription	Psoas Muscle	Psoas
6	chr10:5914000-5929600	Weak transcription	NHLF	lung
7	chr10:5915600-5924400	Weak transcription	Fetal Brain Male	brain
8	chr10:5915600-5930000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
9	chr10:5915600-5930000	Weak transcription	HUVEC	blood vessel
10	chr10:5915800-5930000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
11	chr10:5915800-5930200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
12	chr10:5916000-5921000	Weak transcription	Primary T helper cells PMA-I stimulated	--
13	chr10:5916200-5921200	Strong transcription	Colon Smooth Muscle	Colon
14	chr10:5916200-5922000	Strong transcription	Duodenum Smooth Muscle	Duodenum
15	chr10:5916200-5922200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr10:5916200-5922800	Strong transcription	Fetal Stomach	stomach
17	chr10:5916200-5923000	Strong transcription	HUES6 Cell Line	embryonic stem cell
18	chr10:5916200-5923000	Strong transcription	Brain Inferior Temporal Lobe	brain
19	chr10:5916200-5923000	Strong transcription	Stomach Smooth Muscle	stomach
20	chr10:5916200-5925200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr10:5916200-5926400	Strong transcription	Skeletal Muscle Male	skeletal muscle
22	chr10:5916200-5927600	Strong transcription	Fetal Intestine Small	intestine
23	chr10:5916200-5928200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
24	chr10:5916200-5929000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr10:5916200-5929400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
26	chr10:5916200-5929800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr10:5916200-5929800	Strong transcription	Fetal Intestine Large	intestine
28	chr10:5916400-5922000	Strong transcription	Fetal Muscle Leg	muscle
29	chr10:5916400-5922200	Strong transcription	Left Ventricle	heart
30	chr10:5916400-5922400	Weak transcription	Primary B cells from cord blood	blood
31	chr10:5916400-5923000	Strong transcription	Brain Cingulate Gyrus	brain
32	chr10:5916400-5924800	Strong transcription	Liver	Liver
33	chr10:5916400-5928200	Strong transcription	Fetal Brain Female	brain
34	chr10:5916400-5929200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
35	chr10:5916400-5929800	Strong transcription	Fetal Muscle Trunk	muscle
36	chr10:5916600-5922000	Strong transcription	Gastric	stomach
37	chr10:5916600-5922400	Strong transcription	Brain Substantia Nigra	brain
38	chr10:5916600-5928400	Weak transcription	Small Intestine	intestine
39	chr10:5916600-5929400	Strong transcription	HUES48 Cell Line	embryonic stem cell
40	chr10:5916600-5930600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
41	chr10:5916800-5930200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
42	chr10:5917600-5922600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr10:5917800-5922600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
44	chr10:5917800-5927800	Strong transcription	Thymus	Thymus
45	chr10:5917800-5928600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr10:5918000-5921200	Strong transcription	Lung	lung
47	chr10:5918000-5922200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr10:5918000-5922200	Strong transcription	Primary hematopoietic stem cells	blood
49	chr10:5918000-5923000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
50	chr10:5918000-5924600	Strong transcription	Duodenum Mucosa	Duodenum

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