Variant report

Variant	nsv1099
Chromosome Location	chr1:62275317-62315943
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	chr1:62303430-62303834	HepG2	liver:	n/a	n/a
2	BACH1	chr1:62310570-62310571	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr1:62279461-62279505	K562	blood:	n/a	n/a
4	BCL11A	chr1:62310447-62310604	H1-hESC	embryonic stem cell:	n/a	n/a
5	CBX3	chr1:62303297-62303849	HCT-116	colon:	n/a	n/a
6	CEBPB	chr1:62305355-62305743	Hela-S3	cervix:	n/a	chr1:62305500-62305511
7	CEBPB	chr1:62303319-62303710	HepG2	liver:	n/a	n/a
8	CEBPB	chr1:62303363-62303750	HepG2	liver:	n/a	n/a
9	CEBPB	chr1:62303113-62303923	HCT-116	colon:	n/a	n/a
10	CEBPB	chr1:62303296-62303871	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr1:62303372-62303583	K562	blood:	n/a	n/a
12	CEBPB	chr1:62305274-62305889	HCT-116	colon:	n/a	chr1:62305500-62305511
13	CEBPB	chr1:62304963-62305198	HepG2	liver:	n/a	n/a
14	CEBPB	chr1:62310615-62310629	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr1:62303341-62303578	HepG2	liver:	n/a	n/a
16	CEBPB	chr1:62299687-62299918	K562	blood:	n/a	n/a
17	CEBPB	chr1:62304907-62305678	IMR90	lung:	n/a	chr1:62305500-62305511
18	CEBPB	chr1:62305316-62305731	HCT-116	colon:	n/a	chr1:62305500-62305511
19	CEBPB	chr1:62303295-62303838	HCT-116	colon:	n/a	n/a
20	CHD1	chr1:62305872-62305917	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr1:62300920-62301070	HCPEpiC	choroid plexus:	n/a	n/a
22	CTCF	chr1:62308695-62308835	GM19238	blood:	n/a	chr1:62308764-62308782 chr1:62308766-62308779 chr1:62308759-62308780
23	CTCF	chr1:62308700-62308850	SAEC	small airway:	n/a	chr1:62308764-62308782 chr1:62308766-62308779 chr1:62308759-62308780
24	CTCF	chr1:62308620-62308770	NHDF-neo	bronchial:	n/a	n/a
25	CTCF	chr1:62308640-62308790	BE2_C	brain:	n/a	chr1:62308764-62308782 chr1:62308766-62308779 chr1:62308759-62308780
26	CTCF	chr1:62308680-62308830	HVMF	connective:	n/a	chr1:62308764-62308782 chr1:62308766-62308779 chr1:62308759-62308780
27	CTCF	chr1:62308680-62308830	K562	blood:	n/a	chr1:62308764-62308782 chr1:62308766-62308779 chr1:62308759-62308780
28	CTCF	chr1:62308780-62308930	NHEK	skin:	n/a	n/a
29	CTCF	chr1:62308691-62308884	HepG2	liver:	n/a	chr1:62308764-62308782 chr1:62308766-62308779 chr1:62308759-62308780
30	CTCF	chr1:62308640-62308790	NHLF	lung:	n/a	chr1:62308764-62308782 chr1:62308766-62308779 chr1:62308759-62308780
31	CTCF	chr1:62308700-62308850	AG09319	gingival:	n/a	chr1:62308764-62308782 chr1:62308766-62308779 chr1:62308759-62308780
32	CTCF	chr1:62307840-62307990	AoAF	blood vessel:	n/a	n/a
33	CTCF	chr1:62301324-62301358	Fibrobl	skin:	n/a	n/a
34	CTCF	chr1:62308700-62308850	Caco-2	colon:	n/a	chr1:62308764-62308782 chr1:62308766-62308779 chr1:62308759-62308780
35	CTCF	chr1:62308680-62308830	AoAF	blood vessel:	n/a	chr1:62308764-62308782 chr1:62308766-62308779 chr1:62308759-62308780
36	CTCF	chr1:62308610-62308890	K562	blood:	n/a	chr1:62308764-62308782 chr1:62308766-62308779 chr1:62308759-62308780
37	CTCF	chr1:62308682-62308886	K562	blood:	n/a	chr1:62308764-62308782 chr1:62308766-62308779 chr1:62308759-62308780
38	CTCF	chr1:62308730-62308810	GM12878	blood:	n/a	chr1:62308764-62308782 chr1:62308766-62308779 chr1:62308759-62308780
39	CTCF	chr1:62308668-62308847	MCF-7	breast:	n/a	chr1:62308764-62308782 chr1:62308766-62308779 chr1:62308759-62308780
40	CTCF	chr1:62308680-62308830	GM06990	blood:	n/a	chr1:62308764-62308782 chr1:62308766-62308779 chr1:62308759-62308780
41	CTCF	chr1:62308642-62308886	Gliobla	brain:	n/a	chr1:62308764-62308782 chr1:62308766-62308779 chr1:62308759-62308780
42	CTCF	chr1:62308720-62308870	HPF	lung:	n/a	chr1:62308764-62308782 chr1:62308766-62308779 chr1:62308759-62308780
43	CTCF	chr1:62308720-62308870	HAc	cerebellar:	n/a	chr1:62308764-62308782 chr1:62308766-62308779 chr1:62308759-62308780
44	CTCF	chr1:62308720-62308870	WERI-Rb-1	eye:	n/a	chr1:62308764-62308782 chr1:62308766-62308779 chr1:62308759-62308780
45	CTCF	chr1:62308719-62308823	Kidney_OC	kidney:	n/a	chr1:62308764-62308782 chr1:62308766-62308779 chr1:62308759-62308780
46	CTCF	chr1:62308619-62308913	IMR90	lung:	n/a	chr1:62308764-62308782 chr1:62308766-62308779 chr1:62308759-62308780
47	CTCF	chr1:62308740-62308890	RPTEC	kidney:	n/a	chr1:62308764-62308782 chr1:62308766-62308779 chr1:62308759-62308780
48	CTCF	chr1:62308680-62308830	HBMEC	blood vessel:	n/a	chr1:62308764-62308782 chr1:62308766-62308779 chr1:62308759-62308780
49	CTCF	chr1:62308700-62308850	HCFaa	heart:	n/a	chr1:62308764-62308782 chr1:62308766-62308779 chr1:62308759-62308780
50	CTCF	chr1:62308760-62308910	WI-38	lung:	n/a	chr1:62308764-62308782 chr1:62308766-62308779

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:62311238-62311288	AG09309	skin:	n/a
2	chr1:62311238-62311288	BJ	skin:	n/a
3	chr1:62311238-62311288	GM19239	blood:	n/a
4	chr1:62311238-62311288	HAEpiC	amniotic membrane:	n/a
5	chr1:62311238-62311288	GM06990	blood:	n/a
6	chr1:62311238-62311288	AG04449	skin:	fetal
7	chr1:62311238-62311288	SK-N-MC	brain:	n/a
8	chr1:62311238-62311288	SAEC	small airway:	n/a
9	chr1:62311238-62311288	HRCEpiC	kidney:	n/a
10	chr1:62311238-62311288	SKMC	muscle:	n/a
11	chr1:62311238-62311288	NT2-D1	testis:	n/a
12	chr1:62311238-62311288	Caco-2	colon:	n/a
13	chr1:62311238-62311288	GM12878	blood:	n/a
14	chr1:62311238-62311288	AoSMC	blood vessel:	n/a
15	chr1:62311238-62311288	HCPEpiC	choroid plexus:	n/a
16	chr1:62311238-62311288	PANC-1	pancreas:	n/a
17	chr1:62311238-62311288	PFSK-1	brain:	n/a
18	chr1:62311238-62311288	NHDF-neo	bronchial:	n/a
19	chr1:62311238-62311288	MCF-7	breast:	n/a
20	chr1:62311238-62311288	SK-N-SH	brain:	n/a
21	chr1:62311238-62311288	HCT-116	colon:	n/a
22	chr1:62311238-62311288	T-47D	breast:	n/a
23	chr1:62311238-62311288	PrEC	prostate:	n/a
24	chr1:62311238-62311288	HPAEpiC	pulmonary alveolar:	n/a
25	chr1:62311238-62311288	ovcar-3	ovarian:	n/a
26	chr1:62311238-62311288	GM12891	blood:	n/a
27	chr1:62311238-62311288	HIPEpiC	eye:	n/a
28	chr1:62311238-62311288	U87	brain:	n/a
29	chr1:62311238-62311288	HEEpiC	esophagus:	n/a
30	chr1:62311238-62311288	H1-hESC	embryonic stem cell:	embryo
31	chr1:62311238-62311288	Hela-S3	cervix:	n/a
32	chr1:62311238-62311288	HRE	kidney:	n/a
33	chr1:62311238-62311288	K562	blood:	n/a
34	chr1:62311238-62311288	AG10803	skin:	n/a
35	chr1:62311238-62311288	ProgFib	skin:	n/a
36	chr1:62311238-62311288	Jurkat	blood:	n/a
37	chr1:62311238-62311288	NHBE	bronchial:	n/a
38	chr1:62311238-62311288	HMEC	breast:	n/a
39	chr1:62311238-62311288	MCF10A-Er-Src	breast:	n/a
40	chr1:62311238-62311288	HNPCEpiC	eye:	n/a
41	chr1:62311238-62311288	HCF	heart:	n/a
42	chr1:62311238-62311288	ECC-1	luminal epithelium:	n/a
43	chr1:62311238-62311288	AG09319	gingival:	n/a
44	chr1:62311238-62311288	SK-N-SH_RA	brain:	n/a
45	chr1:62311238-62311288	GM12892	blood:	n/a
46	chr1:62311238-62311288	NB4	blood:	n/a
47	chr1:62311238-62311288	NH-A	brain:	n/a
48	chr1:62311238-62311288	HepG2	liver:	n/a
49	chr1:62311238-62311288	Hepatocyte	liver:	n/a
50	chr1:62311238-62311288	HL-60	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:62313339..62316037-chr1:62320752..62322318,2	MCF-7	breast:
2	chr1:62288601..62290902-chr1:62291765..62293446,2	K562	blood:
3	chr1:62294253..62296248-chr1:62299623..62302341,2	K562	blood:
4	chr1:62188330..62190848-chr1:62304902..62307738,2	K562	blood:
5	chr1:62208685..62210922-chr1:62306053..62308101,2	MCF-7	breast:
6	chr1:62207401..62209297-chr1:62277222..62279728,2	MCF-7	breast:
7	chr1:62294253..62296248-chr1:62299623..62302341,2	K562	blood:
8	chr1:62304428..62307569-chr1:62310144..62313240,3	MCF-7	breast:
9	chr1:62284465..62286145-chr1:62287888..62289486,2	K562	blood:
10	chr1:62304428..62307569-chr1:62310144..62313240,3	MCF-7	breast:
11	chr1:62288601..62290902-chr1:62291765..62293446,2	K562	blood:
12	chr1:62270101..62271801-chr1:62272747..62275462,2	MCF-7	breast:
13	chr1:62284465..62286145-chr1:62287888..62289486,2	K562	blood:

Variant related genes	Relation type
RNU6-414P	TF binding region
RNU6-1177P	TF binding region
RNU6-414P	CpG island
RNU6-1177P	CpG island
ENSG00000271200	chromatin interactions
ENSG00000162604	chromatin interactions
ENSG00000132849	chromatin interactions

Extended variants
information (count: 1477 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:1477 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs554690037	chr1:62275350-62275351	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs575986770	chr1:62275420-62275421	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs543548496	chr1:62275449-62275450	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs565034428	chr1:62275461-62275462	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs188267105	chr1:62275491-62275492	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs544859252	chr1:62275498-62275499	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs34929042	chr1:62275523-62275524	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs560259347	chr1:62275672-62275673	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs377304411	chr1:62275676-62275677	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs11580167	chr1:62275684-62275685	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs549213237	chr1:62275687-62275688	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs374763251	chr1:62275696-62275697	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs368798056	chr1:62275742-62275743	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs140801325	chr1:62275769-62275770	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs564206528	chr1:62275784-62275785	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs531716359	chr1:62275811-62275812	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs552358014	chr1:62275814-62275815	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs539258076	chr1:62275866-62275867	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs547692586	chr1:62275881-62275882	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs61770137	chr1:62275898-62275899	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs536550633	chr1:62275899-62275900	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs72929655	chr1:62275913-62275914	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs1286834	chr1:62275994-62275995	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs576073208	chr1:62276016-62276017	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs537024218	chr1:62276036-62276037	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs191529990	chr1:62276045-62276046	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs576939784	chr1:62276079-62276080	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs541486667	chr1:62276103-62276104	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs370519156	chr1:62276142-62276143	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs184848021	chr1:62276159-62276160	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs34202517	chr1:62276181-62276182	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs111570469	chr1:62276195-62276196	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs531363424	chr1:62276224-62276225	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs189522478	chr1:62276230-62276231	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs138388192	chr1:62276242-62276243	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs141394310	chr1:62276244-62276245	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs79994000	chr1:62276268-62276269	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs566180150	chr1:62276283-62276284	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs530309302	chr1:62276298-62276299	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs548497584	chr1:62276300-62276301	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs564989423	chr1:62276310-62276311	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs181698016	chr1:62276324-62276325	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs373057973	chr1:62276341-62276342	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs578110097	chr1:62276372-62276373	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs558550404	chr1:62276375-62276376	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs570777423	chr1:62276400-62276401	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs534817237	chr1:62276403-62276404	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs545540396	chr1:62276408-62276409	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs35559661	chr1:62276409-62276410	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs186765625	chr1:62276411-62276412	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

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
Medullary thyroid carcinoma	18765511	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:515 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:62220200-62290200	Weak transcription	Lung	lung
2	chr1:62220200-62310800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr1:62222000-62293000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr1:62224000-62290800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr1:62225000-62284400	Weak transcription	Psoas Muscle	Psoas
6	chr1:62227800-62294600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr1:62228600-62391800	Weak transcription	Small Intestine	intestine
8	chr1:62233400-62288800	Weak transcription	Brain Hippocampus Middle	brain
9	chr1:62235400-62288800	Weak transcription	A549	lung
10	chr1:62247600-62287400	Weak transcription	Primary hematopoietic stem cells	blood
11	chr1:62247600-62297400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr1:62250000-62302800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr1:62251200-62288600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
14	chr1:62251200-62306400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
15	chr1:62252000-62275800	Weak transcription	Brain Cingulate Gyrus	brain
16	chr1:62253600-62297400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
17	chr1:62253800-62289000	Weak transcription	HepG2	liver
18	chr1:62254000-62286400	Weak transcription	Aorta	Aorta
19	chr1:62254000-62288600	Weak transcription	Primary B cells from peripheral blood	blood
20	chr1:62254200-62288400	Weak transcription	Adipose Nuclei	Adipose
21	chr1:62255600-62302400	Weak transcription	Brain Anterior Caudate	brain
22	chr1:62257000-62291600	Weak transcription	Gastric	stomach
23	chr1:62260000-62275600	Weak transcription	Fetal Heart	heart
24	chr1:62263400-62280800	Weak transcription	Esophagus	oesophagus
25	chr1:62263400-62293200	Weak transcription	Duodenum Smooth Muscle	Duodenum
26	chr1:62263600-62288400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
27	chr1:62263800-62303800	Weak transcription	Pancreatic Islets	Pancreatic Islet
28	chr1:62263800-62343600	Weak transcription	Colonic Mucosa	Colon
29	chr1:62264200-62290200	Weak transcription	H9 Cell Line	embryonic stem cell
30	chr1:62264600-62283800	Weak transcription	Primary T cells from cord blood	blood
31	chr1:62264600-62286400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr1:62264600-62286400	Weak transcription	Stomach Smooth Muscle	stomach
33	chr1:62264600-62287800	Weak transcription	Left Ventricle	heart
34	chr1:62264600-62292800	Weak transcription	Skeletal Muscle Male	skeletal muscle
35	chr1:62264600-62296000	Weak transcription	Fetal Brain Female	brain
36	chr1:62264600-62297400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
37	chr1:62264600-62321600	Weak transcription	Pancreas	Pancrea
38	chr1:62264600-62335600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
39	chr1:62264800-62276400	Weak transcription	Duodenum Mucosa	Duodenum
40	chr1:62265200-62293000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr1:62265400-62293200	Weak transcription	Fetal Stomach	stomach
42	chr1:62265600-62284000	Weak transcription	H1 Cell Line	embryonic stem cell
43	chr1:62265600-62288400	Weak transcription	Placenta Amnion	Placenta Amnion
44	chr1:62266000-62284400	Weak transcription	Fetal Kidney	kidney
45	chr1:62266600-62288200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr1:62267200-62277400	Weak transcription	GM12878-XiMat	blood
47	chr1:62268800-62277800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr1:62270200-62277800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
49	chr1:62270800-62290200	Weak transcription	Stomach Mucosa	stomach
50	chr1:62271400-62276000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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