Variant report

Variant	nsv1007318
Chromosome Location	chr1:62083960-62113102
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	chr1:62112891-62113154	HepG2	liver:	n/a	n/a
2	ATF1	chr1:62106776-62107045	K562	blood:	n/a	n/a
3	ATF2	chr1:62107397-62107804	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr1:62106882-62107105	K562	blood:	n/a	n/a
5	BHLHE40	chr1:62098847-62098861	K562	blood:	n/a	n/a
6	BHLHE40	chr1:62107382-62107766	K562	blood:	n/a	chr1:62107530-62107546
7	BHLHE40	chr1:62106799-62107118	K562	blood:	n/a	n/a
8	CBX3	chr1:62107266-62107746	K562	blood:	n/a	n/a
9	CCNT2	chr1:62107450-62107689	K562	blood:	n/a	chr1:62107646-62107655
10	CEBPB	chr1:62103904-62104253	HepG2	liver:	n/a	n/a
11	CEBPB	chr1:62090802-62090847	A549	lung:	n/a	n/a
12	CEBPB	chr1:62103922-62104265	A549	lung:	n/a	n/a
13	CEBPB	chr1:62093161-62093304	K562	blood:	n/a	n/a
14	CEBPB	chr1:62103903-62104255	IMR90	lung:	n/a	n/a
15	CEBPB	chr1:62101288-62101356	A549	lung:	n/a	n/a
16	CEBPB	chr1:62108063-62109003	MCF-7	breast:	n/a	n/a
17	CEBPB	chr1:62107061-62107294	K562	blood:	n/a	n/a
18	CEBPB	chr1:62103933-62104217	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr1:62094958-62095094	K562	blood:	n/a	n/a
20	CEBPB	chr1:62108004-62108991	MCF-7	breast:	n/a	n/a
21	CEBPB	chr1:62103918-62104248	K562	blood:	n/a	n/a
22	CHD1	chr1:62107411-62107699	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD1	chr1:62107168-62107238	GM12878	blood:	n/a	n/a
24	CHD2	chr1:62107400-62107674	H1-hESC	embryonic stem cell:	n/a	n/a
25	CREB1	chr1:62107427-62107745	A549	lung:	n/a	n/a
26	CTCF	chr1:62107520-62107670	GM06990	blood:	n/a	chr1:62107580-62107598 chr1:62107575-62107596
27	CTCF	chr1:62107540-62107690	WI-38	lung:	n/a	chr1:62107580-62107598 chr1:62107575-62107596
28	CTCF	chr1:62107500-62107650	Caco-2	colon:	n/a	chr1:62107580-62107598 chr1:62107575-62107596
29	CTCF	chr1:62107540-62107690	AG04450	lung:	n/a	chr1:62107580-62107598 chr1:62107575-62107596
30	CTCF	chr1:62107308-62107741	K562	blood:	n/a	chr1:62107580-62107598 chr1:62107575-62107596
31	CTCF	chr1:62107443-62107715	Spleen_OC	spleen:	n/a	chr1:62107580-62107598 chr1:62107575-62107596
32	CTCF	chr1:62107540-62107690	RPTEC	kidney:	n/a	chr1:62107580-62107598 chr1:62107575-62107596
33	CTCF	chr1:62107540-62107690	HFF-Myc	foreskin:	n/a	chr1:62107580-62107598 chr1:62107575-62107596
34	CTCF	chr1:62107520-62107670	HA-sp	spinal cord:	n/a	chr1:62107580-62107598 chr1:62107575-62107596
35	CTCF	chr1:62107500-62107650	HPF	lung:	n/a	chr1:62107580-62107598 chr1:62107575-62107596
36	CTCF	chr1:62107427-62107724	GM19238	blood:	n/a	chr1:62107580-62107598 chr1:62107575-62107596
37	CTCF	chr1:62107540-62107690	GM12867	blood:	n/a	chr1:62107580-62107598 chr1:62107575-62107596
38	CTCF	chr1:62105460-62105610	AG04450	lung:	n/a	n/a
39	CTCF	chr1:62107520-62107670	HRPEpiC	eye:	n/a	chr1:62107580-62107598 chr1:62107575-62107596
40	CTCF	chr1:62107327-62107691	MCF-7	breast:	n/a	chr1:62107580-62107598 chr1:62107575-62107596
41	CTCF	chr1:62107520-62107670	AG04450	lung:	n/a	chr1:62107580-62107598 chr1:62107575-62107596
42	CTCF	chr1:62107487-62107685	MCF-7	breast:	n/a	chr1:62107580-62107598 chr1:62107575-62107596
43	CTCF	chr1:62107520-62107670	GM12875	blood:	n/a	chr1:62107580-62107598 chr1:62107575-62107596
44	CTCF	chr1:62107480-62107630	Hela-S3	cervix:	n/a	chr1:62107580-62107598 chr1:62107575-62107596
45	CTCF	chr1:62107480-62107630	HEK293	kidney:	n/a	chr1:62107580-62107598 chr1:62107575-62107596
46	CTCF	chr1:62107479-62107696	Pancreas_OC	pancreas:	n/a	chr1:62107580-62107598 chr1:62107575-62107596
47	CTCF	chr1:62107520-62107670	BJ	skin:	n/a	chr1:62107580-62107598 chr1:62107575-62107596
48	CTCF	chr1:62086380-62086530	AG10803	skin:	n/a	n/a
49	CTCF	chr1:62107432-62107727	GM12878	blood:	n/a	chr1:62107580-62107598 chr1:62107575-62107596
50	CTCF	chr1:62107480-62107630	NHEK	skin:	n/a	chr1:62107580-62107598 chr1:62107575-62107596

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:62107430-62107480	NB4	blood:	n/a
2	chr1:62107624-62107674	HRE	kidney:	n/a
3	chr1:62107430-62107480	LNCaP	prostate:	n/a
4	chr1:62102363-62102413	HIPEpiC	eye:	n/a
5	chr1:62102363-62102413	AG09319	gingival:	n/a
6	chr1:62107624-62107674	AG09319	gingival:	n/a
7	chr1:62102363-62102413	SK-N-SH	brain:	n/a
8	chr1:62107430-62107480	AG10803	skin:	n/a
9	chr1:62102363-62102413	K562	blood:	n/a
10	chr1:62107542-62107592	ProgFib	skin:	n/a
11	chr1:62107624-62107674	HCF	heart:	n/a
12	chr1:62107430-62107480	PFSK-1	brain:	n/a
13	chr1:62107430-62107480	HMEC	breast:	n/a
14	chr1:62107542-62107592	HCT-116	colon:	n/a
15	chr1:62107477-62107527	PrEC	prostate:	n/a
16	chr1:62107477-62107527	MCF-7	breast:	n/a
17	chr1:62107430-62107480	HCM	heart:	n/a
18	chr1:62107624-62107674	LNCaP	prostate:	n/a
19	chr1:62107477-62107527	LNCaP	prostate:	n/a
20	chr1:62107477-62107527	AoSMC	blood vessel:	n/a
21	chr1:62102363-62102413	HEK293	kidney:	embryo
22	chr1:62107477-62107527	NT2-D1	testis:	n/a
23	chr1:62107624-62107674	GM19239	blood:	n/a
24	chr1:62107542-62107592	SK-N-SH_RA	brain:	n/a
25	chr1:62102363-62102413	BE2_C	brain:	n/a
26	chr1:62107624-62107674	SK-N-SH_RA	brain:	n/a
27	chr1:62107624-62107674	SAEC	small airway:	n/a
28	chr1:62107430-62107480	HRPEpiC	eye:	n/a
29	chr1:62107430-62107480	HCF	heart:	n/a
30	chr1:62107430-62107480	GM06990	blood:	n/a
31	chr1:62107477-62107527	SK-N-SH_RA	brain:	n/a
32	chr1:62102363-62102413	T-47D	breast:	n/a
33	chr1:62107430-62107480	HCT-116	colon:	n/a
34	chr1:62107542-62107592	GM12878	blood:	n/a
35	chr1:62107624-62107674	HRPEpiC	eye:	n/a
36	chr1:62102363-62102413	Hela-S3	cervix:	n/a
37	chr1:62107624-62107674	K562	blood:	n/a
38	chr1:62107542-62107592	BE2_C	brain:	n/a
39	chr1:62107477-62107527	IMR90	lung:	fetal
40	chr1:62107624-62107674	ECC-1	luminal epithelium:	n/a
41	chr1:62107477-62107527	HEK293	kidney:	embryo
42	chr1:62107430-62107480	ovcar-3	ovarian:	n/a
43	chr1:62107477-62107527	K562	blood:	n/a
44	chr1:62107477-62107527	NH-A	brain:	n/a
45	chr1:62107430-62107480	BJ	skin:	n/a
46	chr1:62107477-62107527	HRCEpiC	kidney:	n/a
47	chr1:62107430-62107480	RPTEC	kidney:	n/a
48	chr1:62107430-62107480	HIPEpiC	eye:	n/a
49	chr1:62107477-62107527	SKMC	muscle:	n/a
50	chr1:62107542-62107592	HRPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:62106350..62108369-chr1:62114638..62116326,2	K562	blood:
2	chr1:62104103..62106324-chr1:62108881..62110470,2	K562	blood:
3	chr1:61519880..61523708-chr1:62105298..62109732,4	MCF-7	breast:
4	chr1:62078266..62080827-chr1:62086486..62088051,2	K562	blood:
5	chr1:62110139..62113045-chr1:62113882..62116057,2	K562	blood:
6	chr1:62104103..62106324-chr1:62108881..62110470,2	K562	blood:
7	chr1:61961790..61962305-chr1:62107717..62108447,2	MCF-7	breast:
8	chr1:62107692..62111975-chr1:62207507..62210400,5	MCF-7	breast:
9	chr1:61681397..61683015-chr1:62107574..62109680,2	MCF-7	breast:
10	chr1:62109498..62111908-chr1:62214585..62216451,2	MCF-7	breast:
11	chr1:62107133..62108121-chr1:62124846..62125524,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-INADL-1	chr1:62102824-62102980	XLOC_000227

Variant related genes	Relation type
ENSG00000264551	TF binding region
ENSG00000264551	CpG island
ENSG00000271200	chromatin interactions
ENSG00000132849	chromatin interactions

Extended variants
information (count: 1125 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:1125 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9629017	chr1:62083960-62083961	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs115124002	chr1:62083980-62083981	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs550905280	chr1:62083988-62083989	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs368023434	chr1:62084040-62084041	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs569269102	chr1:62084085-62084086	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs186545654	chr1:62084126-62084127	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs79397613	chr1:62084137-62084138	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs557949787	chr1:62084195-62084196	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs72921791	chr1:62084210-62084211	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs113343999	chr1:62084223-62084224	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs552859273	chr1:62084238-62084239	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs574348979	chr1:62084262-62084263	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs148867460	chr1:62084282-62084283	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs372052294	chr1:62084327-62084328	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs199604409	chr1:62084354-62084355	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs563258579	chr1:62084382-62084383	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs575113469	chr1:62084405-62084406	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs545910398	chr1:62084415-62084416	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs143541871	chr1:62084431-62084432	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs148040818	chr1:62084456-62084457	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs553494739	chr1:62084458-62084459	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs12036653	chr1:62084461-62084462	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs114237171	chr1:62084464-62084465	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs112750357	chr1:62084479-62084480	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs375894083	chr1:62084500-62084501	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs185433356	chr1:62084501-62084502	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs6694989	chr1:62084503-62084504	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs539447982	chr1:62084569-62084570	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs190885791	chr1:62084620-62084621	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs566587589	chr1:62084681-62084682	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs140898791	chr1:62084704-62084705	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs369052542	chr1:62084730-62084731	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs552724518	chr1:62084761-62084762	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs573453901	chr1:62084768-62084769	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs57436572	chr1:62084771-62084772	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs187352079	chr1:62084795-62084796	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs114637628	chr1:62084810-62084811	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs556951747	chr1:62084874-62084875	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs575240642	chr1:62084906-62084907	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs368025484	chr1:62084915-62084916	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs146659432	chr1:62084916-62084917	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs199666429	chr1:62084917-62084918	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs200652988	chr1:62084918-62084919	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs569324015	chr1:62084930-62084931	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs12732306	chr1:62084935-62084936	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs545471947	chr1:62084941-62084942	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs6695430	chr1:62084979-62084980	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs572927704	chr1:62084982-62084983	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs540850943	chr1:62084983-62084984	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs116494545	chr1:62084990-62084991	Weak transcription Enhancers	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:338 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:62073200-62084400	Weak transcription	Esophagus	oesophagus
2	chr1:62073200-62086400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr1:62073200-62098800	Weak transcription	Right Atrium	heart
4	chr1:62073400-62084200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr1:62079200-62086000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr1:62080400-62086000	Weak transcription	Primary monocytes fromperipheralblood	blood
7	chr1:62080400-62086000	Weak transcription	Monocytes-CD14+_RO01746	blood
8	chr1:62080600-62084400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr1:62082800-62084000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr1:62082800-62084200	Weak transcription	NHEK	skin
11	chr1:62082800-62084400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr1:62082800-62084400	Weak transcription	HMEC	breast
13	chr1:62083000-62084200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr1:62083000-62084200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr1:62083800-62084800	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr1:62084000-62084800	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr1:62084000-62084800	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr1:62084000-62084800	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr1:62084200-62084600	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr1:62084200-62084800	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr1:62084200-62085000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr1:62084200-62085000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr1:62084200-62085000	Enhancers	NHEK	skin
24	chr1:62084200-62085200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr1:62084400-62084600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
26	chr1:62084400-62084600	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr1:62084400-62084800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr1:62084400-62084800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr1:62084400-62084800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr1:62084400-62084800	Enhancers	Breast Myoepithelial Primary Cells	Breast
31	chr1:62084400-62084800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr1:62084400-62084800	Enhancers	Esophagus	oesophagus
33	chr1:62084400-62085000	Enhancers	HMEC	breast
34	chr1:62084600-62084800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr1:62084800-62086200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr1:62085200-62093000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr1:62086000-62086600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr1:62086000-62086600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
39	chr1:62086000-62087400	Enhancers	Primary monocytes fromperipheralblood	blood
40	chr1:62086400-62086600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr1:62086600-62088000	Enhancers	Monocytes-CD14+_RO01746	blood
42	chr1:62090600-62091200	Enhancers	Fetal Lung	lung
43	chr1:62091000-62091200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr1:62091400-62092200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr1:62092200-62093400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr1:62092400-62093000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr1:62092400-62093200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr1:62092600-62093400	Enhancers	Aorta	Aorta
49	chr1:62093400-62096400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr1:62096400-62096600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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