Variant report

Variant	nsv870559
Chromosome Location	chr1:63057136-63113719
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:412)
CpG islands
(count:183)
Chromatin interactive
region (count:18)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:412 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:63087554-63088043	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:63089241-63089296	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:63074554-63075140	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:63059494-63060018	HepG2	liver:	n/a	chr1:63059505-63059521
5	ARID3A	chr1:63079529-63079891	HepG2	liver:	n/a	n/a
6	ATF1	chr1:63087652-63087993	K562	blood:	n/a	n/a
7	ATF2	chr1:63087593-63087996	GM12878	blood:	n/a	n/a
8	ATF2	chr1:63078872-63079532	GM12878	blood:	n/a	n/a
9	ATF2	chr1:63087614-63088085	GM12878	blood:	n/a	n/a
10	ATF3	chr1:63087594-63087996	K562	blood:	n/a	n/a
11	ATF3	chr1:63087530-63087957	A549	lung:	n/a	n/a
12	ATF3	chr1:63087496-63087981	A549	lung:	n/a	n/a
13	BATF	chr1:63064713-63065027	GM12878	blood:	n/a	chr1:63064849-63064860
14	BATF	chr1:63091155-63091470	GM12878	blood:	n/a	n/a
15	BATF	chr1:63087655-63088035	GM12878	blood:	n/a	n/a
16	BATF	chr1:63087603-63088001	GM12878	blood:	n/a	n/a
17	BATF	chr1:63064757-63064998	GM12878	blood:	n/a	chr1:63064849-63064860
18	BCL11A	chr1:63087711-63088043	GM12878	blood:	n/a	n/a
19	BCL11A	chr1:63091142-63091436	GM12878	blood:	n/a	n/a
20	BCL3	chr1:63087446-63088045	A549	lung:	n/a	n/a
21	BCLAF1	chr1:63078822-63079525	GM12878	blood:	n/a	chr1:63079303-63079312
22	BHLHE40	chr1:63097743-63097749	GM12878	blood:	n/a	n/a
23	BHLHE40	chr1:63078977-63079505	GM12878	blood:	n/a	n/a
24	BHLHE40	chr1:63099737-63099778	GM12878	blood:	n/a	n/a
25	BHLHE40	chr1:63087555-63087977	HepG2	liver:	n/a	n/a
26	BHLHE40	chr1:63087611-63088010	GM12878	blood:	n/a	n/a
27	BHLHE40	chr1:63064805-63064823	GM12878	blood:	n/a	n/a
28	BHLHE40	chr1:63087617-63088019	K562	blood:	n/a	n/a
29	BRCA1	chr1:63087609-63087959	Hela-S3	cervix:	n/a	n/a
30	CBX3	chr1:63108951-63109302	K562	blood:	n/a	n/a
31	CBX3	chr1:63087587-63087982	K562	blood:	n/a	n/a
32	CBX3	chr1:63108921-63109372	K562	blood:	n/a	n/a
33	CEBPB	chr1:63087574-63087906	K562	blood:	n/a	n/a
34	CEBPB	chr1:63059466-63059791	HepG2	liver:	n/a	chr1:63059614-63059625 chr1:63059614-63059627
35	CEBPB	chr1:63087542-63087921	A549	lung:	n/a	n/a
36	CEBPB	chr1:63064724-63065042	IMR90	lung:	n/a	n/a
37	CEBPB	chr1:63087591-63087875	HepG2	liver:	n/a	n/a
38	CEBPB	chr1:63087431-63088083	A549	lung:	n/a	n/a
39	CEBPB	chr1:63059453-63059801	H1-hESC	embryonic stem cell:	n/a	chr1:63059614-63059625 chr1:63059614-63059627
40	CEBPB	chr1:63087535-63087961	IMR90	lung:	n/a	n/a
41	CEBPB	chr1:63087586-63087872	HepG2	liver:	n/a	n/a
42	CEBPB	chr1:63111178-63111378	HepG2	liver:	n/a	n/a
43	CEBPB	chr1:63087524-63087970	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr1:63074608-63074964	HepG2	liver:	n/a	n/a
45	CEBPB	chr1:63087515-63087932	MCF-7	breast:	n/a	n/a
46	CEBPB	chr1:63087527-63087965	A549	lung:	n/a	n/a
47	CEBPB	chr1:63059560-63059685	HepG2	liver:	n/a	chr1:63059614-63059625 chr1:63059614-63059627
48	CEBPB	chr1:63079623-63080056	A549	lung:	n/a	n/a
49	CEBPB	chr1:63087525-63087960	HepG2	liver:	n/a	n/a
50	CEBPB	chr1:63067238-63067586	IMR90	lung:	n/a	chr1:63067256-63067268

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:63062489-63062539	Hela-S3	cervix:	n/a
2	chr1:63062489-63062539	H1-hESC	embryonic stem cell:	embryo
3	chr1:63062724-63062774	HCM	heart:	n/a
4	chr1:63062489-63062539	AoSMC	blood vessel:	n/a
5	chr1:63062212-63062262	BE2_C	brain:	n/a
6	chr1:63062724-63062774	Hela-S3	cervix:	n/a
7	chr1:63062724-63062774	HEK293	kidney:	embryo
8	chr1:63062212-63062262	MCF10A-Er-Src	breast:	n/a
9	chr1:63062212-63062262	GM19239	blood:	n/a
10	chr1:63062212-63062262	HUVEC	blood vessel:	n/a
11	chr1:63062489-63062539	HRE	kidney:	n/a
12	chr1:63062724-63062774	SK-N-SH_RA	brain:	n/a
13	chr1:63062724-63062774	HEEpiC	esophagus:	n/a
14	chr1:63062489-63062539	GM19239	blood:	n/a
15	chr1:63062724-63062774	NH-A	brain:	n/a
16	chr1:63062489-63062539	NB4	blood:	n/a
17	chr1:63062212-63062262	HCF	heart:	n/a
18	chr1:63062212-63062262	AoSMC	blood vessel:	n/a
19	chr1:63062212-63062262	HCM	heart:	n/a
20	chr1:63062212-63062262	AG04450	lung:	fetal
21	chr1:63062212-63062262	HMEC	breast:	n/a
22	chr1:63062724-63062774	LNCaP	prostate:	n/a
23	chr1:63062489-63062539	HAEpiC	amniotic membrane:	n/a
24	chr1:63062489-63062539	SK-N-SH_RA	brain:	n/a
25	chr1:63062724-63062774	AG04450	lung:	fetal
26	chr1:63062212-63062262	NHBE	bronchial:	n/a
27	chr1:63062489-63062539	GM12878	blood:	n/a
28	chr1:63062489-63062539	GM06990	blood:	n/a
29	chr1:63062489-63062539	HEEpiC	esophagus:	n/a
30	chr1:63062212-63062262	PrEC	prostate:	n/a
31	chr1:63062212-63062262	HIPEpiC	eye:	n/a
32	chr1:63062724-63062774	HL-60	blood:	n/a
33	chr1:63062489-63062539	HPAEpiC	pulmonary alveolar:	n/a
34	chr1:63062724-63062774	HRPEpiC	eye:	n/a
35	chr1:63062212-63062262	HCPEpiC	choroid plexus:	n/a
36	chr1:63062489-63062539	PFSK-1	brain:	n/a
37	chr1:63062212-63062262	PANC-1	pancreas:	n/a
38	chr1:63062724-63062774	HAEpiC	amniotic membrane:	n/a
39	chr1:63062724-63062774	GM12891	blood:	n/a
40	chr1:63062724-63062774	K562	blood:	n/a
41	chr1:63062489-63062539	AG10803	skin:	n/a
42	chr1:63062489-63062539	BJ	skin:	n/a
43	chr1:63062489-63062539	MCF-7	breast:	n/a
44	chr1:63062724-63062774	T-47D	breast:	n/a
45	chr1:63062489-63062539	Caco-2	colon:	n/a
46	chr1:63062212-63062262	SAEC	small airway:	n/a
47	chr1:63062212-63062262	HEK293	kidney:	embryo
48	chr1:63062489-63062539	SKMC	muscle:	n/a
49	chr1:63062489-63062539	BE2_C	brain:	n/a
50	chr1:63062724-63062774	AoSMC	blood vessel:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:63088603..63091388-chr1:63093156..63095465,2	K562	blood:
2	chr1:63079121..63081577-chr1:63084088..63085604,2	MCF-7	breast:
3	chr1:63104828..63107680-chr1:63108196..63110831,3	K562	blood:
4	chr1:63088346..63090747-chr1:63093561..63095201,2	K562	blood:
5	chr1:63081752..63083296-chr1:63090887..63092573,2	MCF-7	breast:
6	chr1:63082239..63084843-chr1:63153676..63156091,2	K562	blood:
7	chr1:63065055..63067391-chr1:63081562..63083375,2	K562	blood:
8	chr1:63063122..63065536-chr1:63066571..63069108,3	K562	blood:
9	chr1:63088346..63090747-chr1:63093561..63095201,2	K562	blood:
10	chr1:63081404..63083878-chr1:63086190..63087709,2	K562	blood:
11	chr1:63063894..63067391-chr1:63081562..63083857,3	K562	blood:
12	chr1:63063122..63065536-chr1:63066571..63069108,3	K562	blood:
13	chr1:63081752..63083296-chr1:63090887..63092573,2	MCF-7	breast:
14	chr1:63081404..63083878-chr1:63086190..63087709,2	K562	blood:
15	chr1:63088603..63091388-chr1:63093156..63095465,2	K562	blood:
16	chr1:63062723..63066181-chr1:63069299..63072097,3	K562	blood:
17	chr1:63079121..63081577-chr1:63084088..63085604,2	MCF-7	breast:
18	chr1:63102529..63105125-chr5:46100658..46103318,2	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-USP1-1	chr1:63067440-63067553	NONHSAT003634
2	lnc-USP1-1	chr1:63066705-63066867	NONHSAT003634
3	lnc-USP1-1	chr1:63067956-63068051	NONHSAT003634

No data

Variant related genes	Relation type
ENSG00000269624	TF binding region
DOCK7	TF binding region
ENSG00000213703	TF binding region
ANGPTL3	TF binding region
ENSG00000269624	CpG island
DOCK7	CpG island
ENSG00000213703	CpG island
ANGPTL3	CpG island
ENSG00000132855	chromatin interactions
ENSG00000235545	chromatin interactions
ENSG00000213703	chromatin interactions
ENSG00000116641	chromatin interactions

Extended variants
information (count: 1913 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:1913 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1748199	chr1:63057136-63057137	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs556810218	chr1:63057145-63057146	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs578186839	chr1:63057169-63057170	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs190227129	chr1:63057173-63057174	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs368439670	chr1:63057179-63057180	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs182513667	chr1:63057217-63057218	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs374056085	chr1:63057235-63057236	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs532037522	chr1:63057326-63057327	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs572441671	chr1:63057339-63057340	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs374019188	chr1:63057365-63057366	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs138342468	chr1:63057386-63057387	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs142520872	chr1:63057432-63057433	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs188030319	chr1:63057449-63057450	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs550429496	chr1:63057499-63057500	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs193094848	chr1:63057522-63057523	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs184067312	chr1:63057665-63057666	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs146704009	chr1:63057730-63057731	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs546479237	chr1:63057867-63057868	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs139268240	chr1:63057959-63057960	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs187398551	chr1:63057972-63057973	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs546685338	chr1:63057996-63057997	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs192243396	chr1:63058004-63058005	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs548724105	chr1:63058063-63058064	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs115874988	chr1:63058120-63058121	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs538164587	chr1:63058193-63058194	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs143063283	chr1:63058215-63058216	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs75964045	chr1:63058228-63058229	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs571914341	chr1:63058318-63058319	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs539223626	chr1:63058334-63058335	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs536674636	chr1:63058345-63058346	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs554338615	chr1:63058350-63058351	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs552233515	chr1:63058465-63058466	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs565179938	chr1:63058484-63058485	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs572424994	chr1:63058533-63058534	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs543083399	chr1:63058592-63058593	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs372853208	chr1:63058597-63058598	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs76230753	chr1:63058628-63058629	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs544105559	chr1:63058636-63058637	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs562441591	chr1:63058649-63058650	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs533001474	chr1:63058833-63058834	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs147485917	chr1:63058921-63058922	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs184638437	chr1:63058937-63058938	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs188615314	chr1:63058956-63058957	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs200331874	chr1:63059047-63059048	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs549022207	chr1:63059069-63059070	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs567152294	chr1:63059070-63059071	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs566496327	chr1:63059144-63059145	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs550533552	chr1:63059167-63059168	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs571952835	chr1:63059171-63059172	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs148084549	chr1:63059252-63059253	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Breast cancer	16620391	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Breast cancer	17133270	CNVD
Myelofibrosis	22110671	CNVD
CNS Malformation Syndrome	17530927	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Colorectal cancer	20459617	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1056 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:62939800-63060200	Weak transcription	Small Intestine	intestine
2	chr1:62958200-63061000	Weak transcription	Lung	lung
3	chr1:63007200-63096200	Weak transcription	HUVEC	blood vessel
4	chr1:63010800-63078400	Weak transcription	A549	lung
5	chr1:63017800-63057600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
6	chr1:63021600-63058800	Weak transcription	Stomach Smooth Muscle	stomach
7	chr1:63021600-63061400	Weak transcription	Pancreas	Pancrea
8	chr1:63036800-63058600	Weak transcription	Fetal Brain Female	brain
9	chr1:63036800-63113600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
10	chr1:63038400-63087600	Weak transcription	NHEK	skin
11	chr1:63038400-63095600	Weak transcription	Brain Germinal Matrix	brain
12	chr1:63038600-63083000	Weak transcription	Duodenum Smooth Muscle	Duodenum
13	chr1:63039000-63063400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr1:63039200-63095200	Weak transcription	Ovary	ovary
15	chr1:63041000-63095200	Weak transcription	Fetal Muscle Leg	muscle
16	chr1:63041000-63095600	Weak transcription	Fetal Stomach	stomach
17	chr1:63041400-63059000	Weak transcription	Aorta	Aorta
18	chr1:63042200-63083600	Weak transcription	Fetal Muscle Trunk	muscle
19	chr1:63044000-63076000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr1:63047600-63077000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr1:63050600-63083800	Weak transcription	Rectal Mucosa Donor 29	rectum
22	chr1:63051000-63066400	Weak transcription	NHLF	lung
23	chr1:63051400-63059400	Weak transcription	Pancreatic Islets	Pancreatic Islet
24	chr1:63051400-63062800	Weak transcription	Psoas Muscle	Psoas
25	chr1:63051800-63057600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr1:63051800-63075800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr1:63051800-63077000	Weak transcription	Primary hematopoietic stem cells	blood
28	chr1:63051800-63083400	Weak transcription	Fetal Lung	lung
29	chr1:63051800-63096000	Weak transcription	Left Ventricle	heart
30	chr1:63052000-63062200	Weak transcription	Cortex derived primary cultured neurospheres	brain
31	chr1:63052400-63062400	Weak transcription	Fetal Intestine Small	intestine
32	chr1:63052400-63083800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr1:63052600-63058200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr1:63052600-63059400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr1:63052600-63077200	Weak transcription	HSMM	muscle
36	chr1:63052600-63084400	Weak transcription	Rectal Mucosa Donor 31	rectum
37	chr1:63052800-63059600	Weak transcription	HUES64 Cell Line	embryonic stem cell
38	chr1:63052800-63062400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr1:63052800-63067000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr1:63053000-63068000	Weak transcription	NHDF-Ad	bronchial
41	chr1:63053600-63057800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr1:63054600-63064800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr1:63054800-63079800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr1:63054800-63087600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr1:63055200-63063000	Weak transcription	NH-A	brain
46	chr1:63055400-63059400	Weak transcription	Muscle Satellite Cultured Cells	--
47	chr1:63055800-63059400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr1:63056000-63061400	Weak transcription	Fetal Intestine Large	intestine
49	chr1:63056400-63059200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr1:63056400-63059400	Weak transcription	Osteobl	bone

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