Variant report

Variant	nsv1035904
Chromosome Location	chr10:42853677-42929116
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	CBX3	chr10:42863291-42863724	K562	blood:	n/a	n/a
2	CCNT2	chr10:42863141-42863422	K562	blood:	n/a	n/a
3	CCNT2	chr10:42876568-42876697	K562	blood:	n/a	n/a
4	CEBPB	chr10:42926634-42926893	A549	lung:	n/a	chr10:42926737-42926750 chr10:42926737-42926748 chr10:42926738-42926749
5	CEBPB	chr10:42926600-42926883	H1-hESC	embryonic stem cell:	n/a	chr10:42926737-42926750 chr10:42926737-42926748 chr10:42926738-42926749
6	CEBPB	chr10:42926584-42926914	K562	blood:	n/a	chr10:42926737-42926750 chr10:42926737-42926748 chr10:42926738-42926749
7	CEBPB	chr10:42903832-42903893	IMR90	lung:	n/a	chr10:42903853-42903864
8	CEBPB	chr10:42861983-42862018	K562	blood:	n/a	n/a
9	CEBPB	chr10:42886922-42886990	HepG2	liver:	n/a	chr10:42886933-42886944
10	CEBPB	chr10:42926569-42926928	HepG2	liver:	n/a	chr10:42926737-42926750 chr10:42926737-42926748 chr10:42926738-42926749
11	CEBPB	chr10:42862252-42862433	K562	blood:	n/a	n/a
12	CEBPB	chr10:42926636-42926923	MCF-7	breast:	n/a	chr10:42926737-42926750 chr10:42926737-42926748 chr10:42926738-42926749
13	CEBPB	chr10:42926575-42926908	IMR90	lung:	n/a	chr10:42926737-42926750 chr10:42926737-42926748 chr10:42926738-42926749
14	CEBPB	chr10:42926607-42926907	Hela-S3	cervix:	n/a	chr10:42926737-42926750 chr10:42926737-42926748 chr10:42926738-42926749
15	CEBPB	chr10:42903805-42903926	HepG2	liver:	n/a	chr10:42903853-42903864
16	CEBPB	chr10:42926561-42926923	ECC-1	luminal epithelium:	n/a	chr10:42926737-42926750 chr10:42926737-42926748 chr10:42926738-42926749
17	CEBPB	chr10:42926578-42926926	A549	lung:	n/a	chr10:42926737-42926750 chr10:42926737-42926748 chr10:42926738-42926749
18	CEBPB	chr10:42855339-42855578	HepG2	liver:	n/a	chr10:42855468-42855479 chr10:42855470-42855479 chr10:42855468-42855481 chr10:42855469-42855480
19	CEBPB	chr10:42926615-42926811	HepG2	liver:	n/a	chr10:42926737-42926750 chr10:42926737-42926748 chr10:42926738-42926749
20	CEBPB	chr10:42926558-42926930	K562	blood:	n/a	chr10:42926737-42926750 chr10:42926737-42926748 chr10:42926738-42926749
21	CEBPB	chr10:42926626-42926861	HepG2	liver:	n/a	chr10:42926737-42926750 chr10:42926737-42926748 chr10:42926738-42926749
22	CEBPB	chr10:42926554-42927004	A549	lung:	n/a	chr10:42926737-42926750 chr10:42926737-42926748 chr10:42926738-42926749
23	CEBPB	chr10:42926541-42926950	ECC-1	luminal epithelium:	n/a	chr10:42926737-42926750 chr10:42926737-42926748 chr10:42926738-42926749
24	CEBPB	chr10:42926578-42926940	MCF-7	breast:	n/a	chr10:42926737-42926750 chr10:42926737-42926748 chr10:42926738-42926749
25	CEBPD	chr10:42876429-42876788	K562	blood:	n/a	n/a
26	CHD2	chr10:42863371-42863685	K562	blood:	n/a	n/a
27	CHD2	chr10:42863523-42863535	GM12878	blood:	n/a	n/a
28	CTCF	chr10:42924100-42924250	BJ	skin:	n/a	n/a
29	CTCF	chr10:42924120-42924270	WERI-Rb-1	eye:	n/a	n/a
30	CTCF	chr10:42924080-42924230	HVMF	connective:	n/a	n/a
31	CTCF	chr10:42856565-42856668	HepG2	liver:	n/a	n/a
32	CTCF	chr10:42924100-42924250	HFF-Myc	foreskin:	n/a	n/a
33	CTCF	chr10:42924080-42924230	GM12874	blood:	n/a	n/a
34	CTCF	chr10:42924103-42924291	MCF-7	breast:	n/a	n/a
35	CTCF	chr10:42856540-42856690	WERI-Rb-1	eye:	n/a	n/a
36	CTCF	chr10:42924029-42924326	GM12878	blood:	n/a	n/a
37	CTCF	chr10:42924080-42924230	GM12870	blood:	n/a	n/a
38	CTCF	chr10:42856540-42856690	HCFaa	heart:	n/a	n/a
39	CTCF	chr10:42924120-42924270	BJ	skin:	n/a	n/a
40	CTCF	chr10:42924100-42924250	HPF	lung:	n/a	n/a
41	CTCF	chr10:42923840-42923990	NHEK	skin:	n/a	n/a
42	CTCF	chr10:42856520-42856670	RPTEC	kidney:	n/a	n/a
43	CTCF	chr10:42862580-42862730	SK-N-SH_RA	brain:	n/a	n/a
44	CTCF	chr10:42924075-42924276	SK-N-SH_RA	brain:	n/a	n/a
45	CTCF	chr10:42906656-42906711	GM13977	blood:	n/a	n/a
46	CTCF	chr10:42924120-42924270	NHDF-neo	bronchial:	n/a	n/a
47	CTCF	chr10:42856520-42856670	HEK293	kidney:	n/a	n/a
48	CTCF	chr10:42924100-42924250	HBMEC	blood vessel:	n/a	n/a
49	CTCF	chr10:42924100-42924250	HRE	kidney:	n/a	n/a
50	CTCF	chr10:42924107-42924291	Kidney_OC	kidney:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:42864633-42864683	HRCEpiC	kidney:	n/a
2	chr10:42864912-42864962	HMEC	breast:	n/a
3	chr10:42863444-42863494	MCF-7	breast:	n/a
4	chr10:42863594-42863644	Hela-S3	cervix:	n/a
5	chr10:42864633-42864683	HNPCEpiC	eye:	n/a
6	chr10:42863594-42863644	HUVEC	blood vessel:	n/a
7	chr10:42863173-42863223	SAEC	small airway:	n/a
8	chr10:42864912-42864962	MCF10A-Er-Src	breast:	n/a
9	chr10:42863539-42863589	Hela-S3	cervix:	n/a
10	chr10:42859004-42859054	HRE	kidney:	n/a
11	chr10:42863068-42863118	CMK	blood:	n/a
12	chr10:42859004-42859054	AoSMC	blood vessel:	n/a
13	chr10:42862876-42862926	H1-hESC	embryonic stem cell:	embryo
14	chr10:42863173-42863223	Caco-2	colon:	n/a
15	chr10:42859004-42859054	NB4	blood:	n/a
16	chr10:42863068-42863118	HCF	heart:	n/a
17	chr10:42863594-42863644	HCM	heart:	n/a
18	chr10:42863594-42863644	NH-A	brain:	n/a
19	chr10:42863068-42863118	PANC-1	pancreas:	n/a
20	chr10:42863068-42863118	Hepatocyte	liver:	n/a
21	chr10:42863594-42863644	A549	lung:	n/a
22	chr10:42863173-42863223	GM06990	blood:	n/a
23	chr10:42863173-42863223	T-47D	breast:	n/a
24	chr10:42863550-42863600	HepG2	liver:	n/a
25	chr10:42864633-42864683	Jurkat	blood:	n/a
26	chr10:42862876-42862926	SK-N-MC	brain:	n/a
27	chr10:42862876-42862926	HRE	kidney:	n/a
28	chr10:42863539-42863589	HEEpiC	esophagus:	n/a
29	chr10:42859004-42859054	HIPEpiC	eye:	n/a
30	chr10:42863594-42863644	CMK	blood:	n/a
31	chr10:42864912-42864962	K562	blood:	n/a
32	chr10:42864633-42864683	GM12878	blood:	n/a
33	chr10:42863508-42863558	AG09309	skin:	n/a
34	chr10:42863508-42863558	AG10803	skin:	n/a
35	chr10:42862876-42862926	GM12878	blood:	n/a
36	chr10:42864633-42864683	SK-N-SH_RA	brain:	n/a
37	chr10:42862876-42862926	HepG2	liver:	n/a
38	chr10:42863539-42863589	HL-60	blood:	n/a
39	chr10:42863539-42863589	BJ	skin:	n/a
40	chr10:42863444-42863494	MCF10A-Er-Src	breast:	n/a
41	chr10:42863068-42863118	HCM	heart:	n/a
42	chr10:42862978-42863028	PFSK-1	brain:	n/a
43	chr10:42863068-42863118	HAEpiC	amniotic membrane:	n/a
44	chr10:42863068-42863118	HRCEpiC	kidney:	n/a
45	chr10:42859004-42859054	HCF	heart:	n/a
46	chr10:42864633-42864683	ProgFib	skin:	n/a
47	chr10:42863068-42863118	Caco-2	colon:	n/a
48	chr10:42859004-42859054	HPAEpiC	pulmonary alveolar:	n/a
49	chr10:42863594-42863644	LNCaP	prostate:	n/a
50	chr10:42864633-42864683	HCPEpiC	choroid plexus:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:42843787..42846463-chr10:42856590..42859504,3	K562	blood:
2	chr10:42861377..42864864-chr10:42876467..42879026,3	K562	blood:
3	chr10:42860335..42863039-chr10:43132551..43135299,2	K562	blood:
4	chr10:42851804..42854724-chr10:42857105..42858652,2	K562	blood:
5	chr10:42851804..42854724-chr10:42857105..42858652,2	K562	blood:
6	chr10:42846704..42848638-chr10:42856458..42859194,2	K562	blood:
7	chr10:42843787..42846463-chr10:42857739..42859504,2	K562	blood:

Variant related genes	Relation type
ENSG00000215146	TF binding region
ENSG00000215146	CpG island
ENSG00000272373	chromatin interactions
ENSG00000196693	chromatin interactions
ENSG00000215146	chromatin interactions

Extended variants
information (count: 598 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:598 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs558051846	chr10:42853683-42853684	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs571489772	chr10:42853753-42853754	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs533930625	chr10:42853816-42853817	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs553598231	chr10:42853843-42853844	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs530544102	chr10:42853864-42853865	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs573668090	chr10:42853875-42853876	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs192965844	chr10:42853884-42853885	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs199884644	chr10:42853885-42853886	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs200259982	chr10:42853947-42853948	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs73255636	chr10:42853993-42853994	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs542302605	chr10:42853995-42853996	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs202151786	chr10:42854010-42854011	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs189172231	chr10:42854012-42854013	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs534517863	chr10:42854018-42854019	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs192255885	chr10:42854039-42854040	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs183767504	chr10:42854041-42854042	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs137895466	chr10:42854049-42854050	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs533351317	chr10:42854054-42854055	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs540780074	chr10:42854055-42854056	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs373084060	chr10:42854063-42854064	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs377554807	chr10:42854066-42854067	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs371148999	chr10:42854072-42854073	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs560428199	chr10:42854115-42854116	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs529366527	chr10:42854116-42854117	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs549145027	chr10:42854117-42854118	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs569290737	chr10:42854136-42854137	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs75463823	chr10:42854137-42854138	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs144611825	chr10:42854166-42854167	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs148869588	chr10:42854168-42854169	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs187010955	chr10:42854184-42854185	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs149426584	chr10:42854196-42854197	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs201500420	chr10:42854243-42854244	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs371890868	chr10:42854252-42854253	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs372845033	chr10:42854269-42854270	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs571528935	chr10:42854271-42854272	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs533784962	chr10:42854333-42854334	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs553927459	chr10:42854486-42854487	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs199638738	chr10:42854492-42854493	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs191701873	chr10:42854500-42854501	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs117637361	chr10:42854523-42854524	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs60607776	chr10:42854608-42854609	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs575652288	chr10:42854653-42854654	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs184205510	chr10:42854708-42854709	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs558038168	chr10:42854756-42854757	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs140925451	chr10:42854763-42854764	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs200933627	chr10:42854766-42854767	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs57409564	chr10:42854767-42854768	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs150280672	chr10:42854768-42854769	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs577914328	chr10:42854813-42854814	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs2466473	chr10:42854816-42854817	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:69)

Disease	PMID	Source
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21509527	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Mental retardation	21062444	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Testicular germ cell tumor	18059402	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Obesity	20622171	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22241247	CNVD
Intellectual disability	21811512	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Obesity	21956041	CNVD
Lung cancer	21569311	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21785460	CNVD
Autism	20531469	CNVD
small cell lung cancer	20016488	CNVD
Cancer	17440070	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Melanoma	20877625	CNVD
Hirschsprung''s Disease	19925665	CNVD
Hirschsprung''s Disease	20456320	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:249 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:42842200-42857600	Weak transcription	Aorta	Aorta
2	chr10:42847000-42860600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr10:42848000-42862600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr10:42848800-42862000	Weak transcription	Stomach Smooth Muscle	stomach
5	chr10:42850600-42862200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
6	chr10:42850600-42862200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr10:42850800-42859200	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr10:42851200-42857600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr10:42851400-42854800	Weak transcription	Duodenum Smooth Muscle	Duodenum
10	chr10:42851800-42854800	Weak transcription	K562	blood
11	chr10:42852200-42862600	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr10:42852600-42853800	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr10:42852600-42853800	ZNF genes & repeats	NHEK	skin
14	chr10:42852800-42853800	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
15	chr10:42853000-42854400	Weak transcription	Left Ventricle	heart
16	chr10:42853200-42855200	Weak transcription	Ovary	ovary
17	chr10:42853200-42856400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr10:42853200-42857800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
19	chr10:42853600-42854800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr10:42853600-42855200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr10:42853600-42856400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr10:42853800-42854200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr10:42853800-42857600	Weak transcription	Pancreatic Islets	Pancreatic Islet
24	chr10:42853800-42857800	Weak transcription	NHEK	skin
25	chr10:42854000-42856800	Weak transcription	Fetal Intestine Large	intestine
26	chr10:42854000-42861600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr10:42854200-42855600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr10:42854200-42862600	Weak transcription	Colon Smooth Muscle	Colon
29	chr10:42854400-42854600	ZNF genes & repeats	Left Ventricle	heart
30	chr10:42854600-42857400	Weak transcription	Left Ventricle	heart
31	chr10:42854800-42855400	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr10:42854800-42855400	Strong transcription	Duodenum Smooth Muscle	Duodenum
33	chr10:42854800-42858800	Strong transcription	K562	blood
34	chr10:42854800-42862600	Weak transcription	Adipose Nuclei	Adipose
35	chr10:42855200-42856600	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr10:42855200-42858200	Strong transcription	Ovary	ovary
37	chr10:42855400-42856000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr10:42855400-42862600	Weak transcription	Duodenum Smooth Muscle	Duodenum
39	chr10:42855600-42856400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr10:42855600-42862600	Weak transcription	Brain Angular Gyrus	brain
41	chr10:42855800-42857800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr10:42856000-42858800	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr10:42856200-42856400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr10:42856400-42857400	Weak transcription	Pancreas	Pancrea
45	chr10:42856400-42858800	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr10:42856400-42859200	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr10:42856600-42856800	ZNF genes & repeats	Fetal Brain Male	brain
48	chr10:42856600-42857400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr10:42856800-42857800	ZNF genes & repeats	Fetal Intestine Large	intestine
50	chr10:42857000-42858200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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