Variant report

Variant	nsv1011842
Chromosome Location	chr1:62414911-62428530
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	ATF2	chr1:62417577-62418091	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr1:62417538-62418004	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr1:62418881-62419230	IMR90	lung:	n/a	n/a
4	CEBPB	chr1:62418894-62419140	HepG2	liver:	n/a	n/a
5	CEBPB	chr1:62415035-62415226	K562	blood:	n/a	n/a
6	CHD1	chr1:62417310-62417837	H1-hESC	embryonic stem cell:	n/a	n/a
7	CHD1	chr1:62416839-62416933	H1-hESC	embryonic stem cell:	n/a	n/a
8	CHD2	chr1:62417448-62418216	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTCF	chr1:62415658-62415694	Kidney_OC	kidney:	n/a	n/a
10	CTCF	chr1:62416140-62416290	GM06990	blood:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
11	CTCF	chr1:62416180-62416330	AG10803	skin:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
12	CTCF	chr1:62415995-62416610	A549	lung:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
13	CTCF	chr1:62416180-62416330	GM12873	blood:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
14	CTCF	chr1:62416160-62416310	NHEK	skin:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
15	CTCF	chr1:62416101-62416363	SK-N-SH_RA	brain:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
16	CTCF	chr1:62416200-62416350	GM12874	blood:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
17	CTCF	chr1:62416218-62416326	Spleen_OC	spleen:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
18	CTCF	chr1:62416175-62416318	SK-N-SH_RA	brain:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
19	CTCF	chr1:62416180-62416330	NHEK	skin:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
20	CTCF	chr1:62416186-62416325	Pancreas_OC	pancreas:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
21	CTCF	chr1:62416160-62416310	GM12868	blood:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
22	CTCF	chr1:62416120-62416270	HBMEC	blood vessel:	n/a	chr1:62416248-62416266 chr1:62416249-62416265
23	CTCF	chr1:62416100-62416250	GM12872	blood:	n/a	n/a
24	CTCF	chr1:62416180-62416330	GM12869	blood:	n/a	chr1:62416250-62416271 chr1:62416249-62416265 chr1:62416248-62416266
25	CTCF	chr1:62416120-62416270	AG10803	skin:	n/a	chr1:62416248-62416266 chr1:62416249-62416265
26	CTCF	chr1:62416139-62416376	Medullo	brain:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
27	CTCF	chr1:62416220-62416370	AG09319	gingival:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
28	CTCF	chr1:62416180-62416330	HCPEpiC	choroid plexus:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
29	CTCF	chr1:62416140-62416290	GM12867	blood:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
30	CTCF	chr1:62416252-62416276	Gliobla	brain:	n/a	n/a
31	CTCF	chr1:62416160-62416310	HL-60	blood:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
32	CTCF	chr1:62416180-62416330	HEK293	kidney:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
33	CTCF	chr1:62416160-62416310	GM06990	blood:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
34	CTCF	chr1:62416160-62416310	GM12864	blood:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
35	CTCF	chr1:62416260-62416410	RPTEC	kidney:	n/a	n/a
36	CTCF	chr1:62416089-62416375	H1-hESC	embryonic stem cell:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
37	CTCF	chr1:62416135-62416374	K562	blood:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
38	CTCF	chr1:62416140-62416290	SAEC	small airway:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
39	CTCF	chr1:62416080-62416230	HRPEpiC	eye:	n/a	n/a
40	CTCF	chr1:62416221-62416309	MCF-7	breast:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
41	CTCF	chr1:62416180-62416330	SAEC	small airway:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
42	CTCF	chr1:62416100-62416250	SK-N-SH_RA	brain:	n/a	n/a
43	CTCF	chr1:62416180-62416330	HA-sp	spinal cord:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
44	CTCF	chr1:62416162-62416361	Hela-S3	cervix:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
45	CTCF	chr1:62416100-62416250	K562	blood:	n/a	n/a
46	CTCF	chr1:62416160-62416310	RPTEC	kidney:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
47	CTCF	chr1:62416160-62416310	HRPEpiC	eye:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
48	CTCF	chr1:62416065-62416438	GM12878	blood:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
49	CTCF	chr1:62416180-62416330	HEEpiC	esophagus:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265
50	CTCF	chr1:62416190-62416338	HepG2	liver:	n/a	chr1:62416250-62416271 chr1:62416248-62416266 chr1:62416249-62416265

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:62416593-62416643	PrEC	prostate:	n/a
2	chr1:62416593-62416643	AG09309	skin:	n/a
3	chr1:62416593-62416643	HPAEpiC	pulmonary alveolar:	n/a
4	chr1:62416593-62416643	AG09319	gingival:	n/a
5	chr1:62416593-62416643	HEEpiC	esophagus:	n/a
6	chr1:62416593-62416643	HepG2	liver:	n/a
7	chr1:62416593-62416643	ProgFib	skin:	n/a
8	chr1:62416593-62416643	SK-N-SH	brain:	n/a
9	chr1:62416593-62416643	MCF10A-Er-Src	breast:	n/a
10	chr1:62416593-62416643	HAEpiC	amniotic membrane:	n/a
11	chr1:62416593-62416643	GM12891	blood:	n/a
12	chr1:62416593-62416643	H1-hESC	embryonic stem cell:	embryo
13	chr1:62416593-62416643	HUVEC	blood vessel:	n/a
14	chr1:62416593-62416643	ovcar-3	ovarian:	n/a
15	chr1:62416593-62416643	HRCEpiC	kidney:	n/a
16	chr1:62416593-62416643	HCF	heart:	n/a
17	chr1:62416593-62416643	PFSK-1	brain:	n/a
18	chr1:62416593-62416643	GM12878	blood:	n/a
19	chr1:62416593-62416643	HL-60	blood:	n/a
20	chr1:62416593-62416643	K562	blood:	n/a
21	chr1:62416593-62416643	NT2-D1	testis:	n/a
22	chr1:62416593-62416643	HRPEpiC	eye:	n/a
23	chr1:62416593-62416643	BE2_C	brain:	n/a
24	chr1:62416593-62416643	AG10803	skin:	n/a
25	chr1:62416593-62416643	LNCaP	prostate:	n/a
26	chr1:62416593-62416643	CMK	blood:	n/a
27	chr1:62416593-62416643	BJ	skin:	n/a
28	chr1:62416593-62416643	PANC-1	pancreas:	n/a
29	chr1:62416593-62416643	GM12892	blood:	n/a
30	chr1:62416593-62416643	Jurkat	blood:	n/a
31	chr1:62416593-62416643	NH-A	brain:	n/a
32	chr1:62416593-62416643	HNPCEpiC	eye:	n/a
33	chr1:62416593-62416643	SK-N-SH_RA	brain:	n/a
34	chr1:62416593-62416643	T-47D	breast:	n/a
35	chr1:62416593-62416643	NHBE	bronchial:	n/a
36	chr1:62416593-62416643	SAEC	small airway:	n/a
37	chr1:62416593-62416643	HEK293	kidney:	embryo
38	chr1:62416593-62416643	SK-N-MC	brain:	n/a
39	chr1:62416593-62416643	AoSMC	blood vessel:	n/a
40	chr1:62416593-62416643	A549	lung:	n/a
41	chr1:62416593-62416643	GM06990	blood:	n/a
42	chr1:62416593-62416643	HCPEpiC	choroid plexus:	n/a
43	chr1:62416593-62416643	MCF-7	breast:	n/a
44	chr1:62416593-62416643	GM19239	blood:	n/a
45	chr1:62416593-62416643	SKMC	muscle:	n/a
46	chr1:62416593-62416643	ECC-1	luminal epithelium:	n/a
47	chr1:62416593-62416643	RPTEC	kidney:	n/a
48	chr1:62416593-62416643	HCT-116	colon:	n/a
49	chr1:62416593-62416643	AG04449	skin:	fetal
50	chr1:62416593-62416643	Caco-2	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:62420887..62422924-chr1:62423218..62424749,2	MCF-7	breast:
2	chr1:62420887..62422924-chr1:62423218..62424749,2	MCF-7	breast:
3	chr1:62417324..62419162-chr1:62419469..62421904,2	MCF-7	breast:

Variant related genes	Relation type
INADL	TF binding region
INADL	CpG island
ENSG00000132849	chromatin interactions

Extended variants
information (count: 448 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:448 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs576921470	chr1:62414933-62414934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs541222746	chr1:62414955-62414956	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs189277898	chr1:62414958-62414959	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs9436654	chr1:62414980-62414981	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs137918155	chr1:62414982-62414983	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs562917108	chr1:62414993-62414994	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs530544560	chr1:62415005-62415006	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs28405010	chr1:62415039-62415040	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs11804624	chr1:62415077-62415078	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs142479580	chr1:62415078-62415079	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs149121207	chr1:62415086-62415087	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs34849424	chr1:62415087-62415088	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs58970353	chr1:62415088-62415089	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs532377324	chr1:62415094-62415095	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs541304416	chr1:62415102-62415103	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs528833171	chr1:62415113-62415114	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs2482874	chr1:62415176-62415177	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs145977074	chr1:62415207-62415208	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs11809363	chr1:62415283-62415284	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs551113554	chr1:62415300-62415301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs569239945	chr1:62415376-62415377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs2498959	chr1:62415381-62415382	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs558523182	chr1:62415387-62415388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs2482876	chr1:62415430-62415431	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs34281635	chr1:62415503-62415504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs397808345	chr1:62415504-62415505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs57372686	chr1:62415507-62415508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs534651899	chr1:62415515-62415516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs190119120	chr1:62415525-62415526	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs181607298	chr1:62415534-62415535	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs574314063	chr1:62415537-62415538	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs12074521	chr1:62415552-62415553	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs185543257	chr1:62415629-62415630	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs150691548	chr1:62415645-62415646	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs545783549	chr1:62415731-62415732	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs549114567	chr1:62415770-62415771	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs563968546	chr1:62415780-62415781	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs67395722	chr1:62415789-62415790	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs533742602	chr1:62415807-62415808	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs562232464	chr1:62415808-62415809	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs190203099	chr1:62415817-62415818	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs12069359	chr1:62415825-62415826	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs371561339	chr1:62415862-62415863	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs116205959	chr1:62415982-62415983	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs181424183	chr1:62416020-62416021	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs551741950	chr1:62416026-62416027	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs566786396	chr1:62416043-62416044	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs147515167	chr1:62416082-62416083	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs552865491	chr1:62416090-62416091	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs567874281	chr1:62416093-62416094	Enhancers Weak transcription	TF binding region	1 gene(s)	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
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:190 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:62346200-62417600	Weak transcription	Rectal Smooth Muscle	rectum
2	chr1:62350600-62428200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
3	chr1:62350800-62417600	Weak transcription	Ovary	ovary
4	chr1:62372400-62417600	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr1:62376200-62417600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr1:62381000-62416000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr1:62381200-62417400	Weak transcription	Skeletal Muscle Female	skeletal muscle
8	chr1:62381200-62418400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
9	chr1:62385000-62494200	Weak transcription	Aorta	Aorta
10	chr1:62393800-62422400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
11	chr1:62396200-62416000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr1:62396200-62417200	Weak transcription	HMEC	breast
13	chr1:62396400-62418000	Weak transcription	Fetal Kidney	kidney
14	chr1:62400600-62417600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr1:62406600-62430200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr1:62407200-62417400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr1:62408800-62416000	Weak transcription	HUES64 Cell Line	embryonic stem cell
18	chr1:62409000-62416000	Weak transcription	HUES48 Cell Line	embryonic stem cell
19	chr1:62409000-62436800	Weak transcription	Primary T helper cells PMA-I stimulated	--
20	chr1:62409200-62416000	Weak transcription	H1 Cell Line	embryonic stem cell
21	chr1:62409200-62416000	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr1:62409200-62416200	Weak transcription	NHEK	skin
23	chr1:62409200-62416600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
24	chr1:62409200-62456000	Weak transcription	Rectal Mucosa Donor 31	rectum
25	chr1:62409200-62456800	Weak transcription	Rectal Mucosa Donor 29	rectum
26	chr1:62409200-62457000	Weak transcription	Fetal Intestine Large	intestine
27	chr1:62409200-62518600	Weak transcription	Pancreas	Pancrea
28	chr1:62409400-62416800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr1:62409400-62417200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr1:62409400-62418000	Weak transcription	Left Ventricle	heart
31	chr1:62409400-62429600	Weak transcription	Gastric	stomach
32	chr1:62409400-62458400	Weak transcription	Sigmoid Colon	Sigmoid Colon
33	chr1:62409600-62417200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr1:62409800-62416600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr1:62410200-62425200	Weak transcription	Fetal Intestine Small	intestine
36	chr1:62416000-62416200	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr1:62416000-62417000	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr1:62416000-62417000	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr1:62416000-62417200	Enhancers	HUES64 Cell Line	embryonic stem cell
40	chr1:62416000-62417200	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr1:62416000-62417800	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr1:62416000-62417800	Enhancers	H1 Cell Line	embryonic stem cell
43	chr1:62416000-62417800	Enhancers	HUES6 Cell Line	embryonic stem cell
44	chr1:62416200-62416400	Enhancers	NH-A	brain
45	chr1:62416200-62416600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
46	chr1:62416200-62418000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr1:62416200-62418600	Enhancers	NHEK	skin
48	chr1:62416400-62416800	Enhancers	HepG2	liver
49	chr1:62416400-62417400	Weak transcription	NH-A	brain
50	chr1:62416600-62416800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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