Variant report

Variant	nsv871250
Chromosome Location	chr1:62769887-62799451
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:329)
CpG islands
(count:856)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:329 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:62785027-62785395	HepG2	liver:	n/a	n/a
2	BRCA1	chr1:62773751-62774246	Hela-S3	cervix:	n/a	n/a
3	BRCA1	chr1:62784036-62784179	HepG2	liver:	n/a	n/a
4	BRCA1	chr1:62787169-62787450	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr1:62784852-62785343	HepG2	liver:	n/a	n/a
6	CEBPB	chr1:62790697-62791060	HepG2	liver:	n/a	chr1:62790867-62790878
7	CEBPB	chr1:62784944-62785359	HepG2	liver:	n/a	n/a
8	CEBPB	chr1:62773707-62774105	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr1:62787251-62787472	A549	lung:	n/a	n/a
10	CEBPB	chr1:62777297-62777609	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr1:62785032-62785313	K562	blood:	n/a	n/a
12	CEBPB	chr1:62790755-62791032	A549	lung:	n/a	chr1:62790867-62790878
13	CEBPB	chr1:62784973-62785355	HepG2	liver:	n/a	n/a
14	CEBPB	chr1:62784929-62785402	ECC-1	luminal epithelium:	n/a	n/a
15	CEBPB	chr1:62790754-62791105	A549	lung:	n/a	chr1:62790867-62790878
16	CEBPB	chr1:62784999-62785311	A549	lung:	n/a	n/a
17	CEBPB	chr1:62790704-62791126	Hela-S3	cervix:	n/a	chr1:62790867-62790878
18	CEBPB	chr1:62784888-62785352	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr1:62787244-62787473	A549	lung:	n/a	n/a
20	CEBPB	chr1:62784980-62785385	A549	lung:	n/a	n/a
21	CEBPB	chr1:62785040-62785323	ECC-1	luminal epithelium:	n/a	n/a
22	CEBPB	chr1:62785014-62785300	HepG2	liver:	n/a	n/a
23	CEBPB	chr1:62784848-62785378	A549	lung:	n/a	n/a
24	CEBPB	chr1:62787066-62787565	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr1:62784975-62785350	MCF-7	breast:	n/a	n/a
26	CEBPD	chr1:62784989-62785316	HepG2	liver:	n/a	n/a
27	CEBPD	chr1:62784803-62785236	HepG2	liver:	n/a	n/a
28	CHD1	chr1:62777455-62777457	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD2	chr1:62787044-62787515	Hela-S3	cervix:	n/a	n/a
30	CHD2	chr1:62784179-62784330	HepG2	liver:	n/a	n/a
31	CHD2	chr1:62773755-62774089	Hela-S3	cervix:	n/a	n/a
32	CHD2	chr1:62790895-62791114	Hela-S3	cervix:	n/a	n/a
33	CREB1	chr1:62784647-62785436	HepG2	liver:	n/a	n/a
34	CREB1	chr1:62784915-62785415	HepG2	liver:	n/a	n/a
35	CTBP2	chr1:62783909-62785025	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr1:62784896-62785001	Fibrobl	skin:	n/a	chr1:62784915-62784925
37	CTCF	chr1:62791040-62791190	SK-N-SH_RA	brain:	n/a	n/a
38	CTCF	chr1:62777340-62777490	HRE	kidney:	n/a	n/a
39	CTCF	chr1:62791420-62791570	HMEC	breast:	n/a	n/a
40	CTCF	chr1:62784860-62785010	SK-N-SH_RA	brain:	n/a	chr1:62784915-62784925
41	CTCF	chr1:62777280-62777430	GM12873	blood:	n/a	n/a
42	CTCF	chr1:62784860-62785010	WERI-Rb-1	eye:	n/a	chr1:62784915-62784925
43	CTCF	chr1:62790396-62790441	Kidney_OC	kidney:	n/a	n/a
44	CTCF	chr1:62784972-62784982	MCF-7	breast:	n/a	n/a
45	CTCF	chr1:62784860-62785010	HepG2	liver:	n/a	chr1:62784915-62784925
46	CTCF	chr1:62784903-62785022	MCF-7	breast:	n/a	chr1:62784915-62784925
47	CTCF	chr1:62777360-62777510	WERI-Rb-1	eye:	n/a	n/a
48	CTCF	chr1:62791460-62791610	HBMEC	blood vessel:	n/a	n/a
49	CTCF	chr1:62784800-62784950	Caco-2	colon:	n/a	chr1:62784915-62784925
50	CTCF	chr1:62784919-62785006	A549	lung:	n/a	n/a

(count:856 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:62784762-62784812	PANC-1	pancreas:	n/a
2	chr1:62784332-62784382	SAEC	small airway:	n/a
3	chr1:62784762-62784812	PANC-1	pancreas:	n/a
4	chr1:62784332-62784382	SAEC	small airway:	n/a
5	chr1:62783533-62783583	HCPEpiC	choroid plexus:	n/a
6	chr1:62785901-62785951	HAEpiC	amniotic membrane:	n/a
7	chr1:62783533-62783583	SKMC	muscle:	n/a
8	chr1:62785079-62785129	SKMC	muscle:	n/a
9	chr1:62785454-62785504	K562	blood:	n/a
10	chr1:62785454-62785504	SKMC	muscle:	n/a
11	chr1:62785698-62785748	GM12892	blood:	n/a
12	chr1:62784802-62784852	GM19239	blood:	n/a
13	chr1:62786082-62786132	NT2-D1	testis:	n/a
14	chr1:62784762-62784812	Caco-2	colon:	n/a
15	chr1:62785512-62785562	ProgFib	skin:	n/a
16	chr1:62785901-62785951	NHDF-neo	bronchial:	n/a
17	chr1:62784269-62784319	ovcar-3	ovarian:	n/a
18	chr1:62784651-62784701	GM12892	blood:	n/a
19	chr1:62784802-62784852	HCT-116	colon:	n/a
20	chr1:62781737-62781787	NHBE	bronchial:	n/a
21	chr1:62784802-62784852	ECC-1	luminal epithelium:	n/a
22	chr1:62786082-62786132	T-47D	breast:	n/a
23	chr1:62781737-62781787	Hela-S3	cervix:	n/a
24	chr1:62785512-62785562	HAEpiC	amniotic membrane:	n/a
25	chr1:62787266-62787316	SK-N-SH	brain:	n/a
26	chr1:62785698-62785748	PANC-1	pancreas:	n/a
27	chr1:62784762-62784812	AG09319	gingival:	n/a
28	chr1:62784651-62784701	HUVEC	blood vessel:	n/a
29	chr1:62786082-62786132	Caco-2	colon:	n/a
30	chr1:62784651-62784701	NT2-D1	testis:	n/a
31	chr1:62781737-62781787	HCT-116	colon:	n/a
32	chr1:62784269-62784319	HCT-116	colon:	n/a
33	chr1:62784762-62784812	MCF-7	breast:	n/a
34	chr1:62785901-62785951	NHBE	bronchial:	n/a
35	chr1:62784762-62784812	HCM	heart:	n/a
36	chr1:62784269-62784319	HMEC	breast:	n/a
37	chr1:62784269-62784319	AG04450	lung:	fetal
38	chr1:62781737-62781787	A549	lung:	n/a
39	chr1:62786082-62786132	MCF10A-Er-Src	breast:	n/a
40	chr1:62785901-62785951	LNCaP	prostate:	n/a
41	chr1:62784802-62784852	Jurkat	blood:	n/a
42	chr1:62787266-62787316	HNPCEpiC	eye:	n/a
43	chr1:62784651-62784701	HAEpiC	amniotic membrane:	n/a
44	chr1:62787266-62787316	MCF-7	breast:	n/a
45	chr1:62784269-62784319	AG10803	skin:	n/a
46	chr1:62785512-62785562	HRCEpiC	kidney:	n/a
47	chr1:62787266-62787316	HUVEC	blood vessel:	n/a
48	chr1:62785079-62785129	PFSK-1	brain:	n/a
49	chr1:62784802-62784852	MCF10A-Er-Src	breast:	n/a
50	chr1:62784762-62784812	IMR90	lung:	fetal

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:62796227..62800204-chr1:62803015..62806082,4	K562	blood:
2	chr1:62786251..62788988-chr1:62790093..62792721,3	MCF-7	breast:
3	chr1:62786251..62788988-chr1:62790093..62792721,3	MCF-7	breast:
4	chr1:62782472..62785250-chr1:62785761..62788536,3	MCF-7	breast:

No data

Variant related genes	Relation type
KANK4	TF binding region
KANK4	CpG island
ENSG00000132854	chromatin interactions

Extended variants
information (count: 1150 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:1150 , 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	rs17123422	chr1:62769887-62769888	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs6587966	chr1:62769931-62769932	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs367626379	chr1:62769935-62769936	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs576043919	chr1:62770007-62770008	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs35985239	chr1:62770113-62770114	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs555074643	chr1:62770180-62770181	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs114173840	chr1:62770212-62770213	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs149770792	chr1:62770225-62770226	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs528684152	chr1:62770236-62770237	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs540684983	chr1:62770285-62770286	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs189911024	chr1:62770308-62770309	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs17123425	chr1:62770334-62770335	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs140386862	chr1:62770380-62770381	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs182191498	chr1:62770381-62770382	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs5774597	chr1:62770399-62770400	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs397706769	chr1:62770402-62770403	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs186326362	chr1:62770453-62770454	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs552083198	chr1:62770454-62770455	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs115021846	chr1:62770459-62770460	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs534527383	chr1:62770551-62770552	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs553004374	chr1:62770583-62770584	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs11809218	chr1:62770624-62770625	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs145591316	chr1:62770629-62770630	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs557038316	chr1:62770715-62770716	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs191467999	chr1:62770716-62770717	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs559155350	chr1:62770748-62770749	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs546432588	chr1:62770801-62770802	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs555716356	chr1:62770841-62770842	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs558179540	chr1:62770851-62770852	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs115167531	chr1:62770858-62770859	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs540490071	chr1:62770923-62770924	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs561823333	chr1:62770930-62770931	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs386631760	chr1:62770963-62770964	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs4915812	chr1:62770965-62770966	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs10710729	chr1:62770981-62770982	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs7368100	chr1:62770990-62770991	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs7367003	chr1:62770991-62770992	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs77463810	chr1:62770997-62770998	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs180732177	chr1:62771010-62771011	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs146523763	chr1:62771011-62771012	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs185128728	chr1:62771012-62771013	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs4915813	chr1:62771019-62771020	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs143137261	chr1:62771040-62771041	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs546512132	chr1:62771045-62771046	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs35669743	chr1:62771050-62771051	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs189842893	chr1:62771062-62771063	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs79314526	chr1:62771065-62771066	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs59712922	chr1:62771088-62771089	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs568833659	chr1:62771110-62771111	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs374042713	chr1:62771114-62771115	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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Chronic lymphocytic leukemia	21546498	CNVD

Chromatin state (count:618 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:62754400-62773400	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr1:62759800-62770800	Enhancers	Fetal Muscle Leg	muscle
3	chr1:62762200-62773200	Weak transcription	Fetal Lung	lung
4	chr1:62766000-62770000	Weak transcription	Fetal Muscle Trunk	muscle
5	chr1:62766000-62770200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr1:62766800-62770200	Weak transcription	Gastric	stomach
7	chr1:62767600-62780600	Weak transcription	HepG2	liver
8	chr1:62768000-62770000	Weak transcription	Pancreas	Pancrea
9	chr1:62768000-62772600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr1:62768000-62773600	Weak transcription	Fetal Stomach	stomach
11	chr1:62768000-62776800	Weak transcription	Fetal Kidney	kidney
12	chr1:62769000-62770000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr1:62769000-62772800	Weak transcription	Adipose Nuclei	Adipose
14	chr1:62770000-62770800	Enhancers	Breast Myoepithelial Primary Cells	Breast
15	chr1:62770000-62771000	Enhancers	Fetal Muscle Trunk	muscle
16	chr1:62770000-62772000	Enhancers	Pancreas	Pancrea
17	chr1:62770200-62770600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr1:62770200-62770800	Enhancers	Gastric	stomach
19	chr1:62770800-62773200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
20	chr1:62770800-62773200	Weak transcription	Fetal Muscle Leg	muscle
21	chr1:62770800-62775600	Weak transcription	Gastric	stomach
22	chr1:62771000-62773200	Weak transcription	Fetal Muscle Trunk	muscle
23	chr1:62772000-62772400	Weak transcription	Pancreas	Pancrea
24	chr1:62772400-62776000	Enhancers	Pancreas	Pancrea
25	chr1:62772600-62774400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr1:62772600-62776400	Enhancers	HMEC	breast
27	chr1:62772600-62776600	Enhancers	Placenta	Placenta
28	chr1:62772800-62776200	Enhancers	Adipose Nuclei	Adipose
29	chr1:62773200-62773400	Enhancers	Fetal Lung	lung
30	chr1:62773200-62773400	Bivalent Enhancer	Stomach Smooth Muscle	stomach
31	chr1:62773200-62773600	Enhancers	Hela-S3	cervix
32	chr1:62773200-62774200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr1:62773200-62774400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
34	chr1:62773200-62774600	Enhancers	Fetal Muscle Leg	muscle
35	chr1:62773200-62774800	Enhancers	Fetal Muscle Trunk	muscle
36	chr1:62773200-62776000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr1:62773200-62776200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr1:62773200-62776200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr1:62773200-62776200	Enhancers	NHEK	skin
40	chr1:62773200-62778600	Enhancers	Breast Myoepithelial Primary Cells	Breast
41	chr1:62773400-62776600	Enhancers	Placenta Amnion	Placenta Amnion
42	chr1:62773400-62780800	Weak transcription	Fetal Lung	lung
43	chr1:62773600-62773800	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr1:62773600-62773800	Enhancers	Fetal Stomach	stomach
45	chr1:62773600-62774200	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chr1:62773600-62774200	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr1:62773600-62774400	Enhancers	Esophagus	oesophagus
48	chr1:62773600-62774400	Flanking Active TSS	Hela-S3	cervix
49	chr1:62773800-62774800	Bivalent Enhancer	Fetal Stomach	stomach
50	chr1:62774000-62774400	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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