Variant report

Variant	nsv1012555
Chromosome Location	chr1:57950355-58103389
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	ATF1	chr1:57980434-57980525	K562	blood:	n/a	n/a
2	ATF1	chr1:58088796-58088953	K562	blood:	n/a	n/a
3	ATF1	chr1:58063178-58063197	K562	blood:	n/a	n/a
4	BACH1	chr1:58088731-58088857	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr1:58086631-58086962	HepG2	liver:	n/a	n/a
6	BHLHE40	chr1:58088727-58088844	HepG2	liver:	n/a	n/a
7	BRCA1	chr1:57983395-57984654	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr1:58102731-58103183	Hela-S3	cervix:	n/a	chr1:58102869-58102880
9	CEBPB	chr1:57964156-57964481	A549	lung:	n/a	chr1:57964306-57964317
10	CEBPB	chr1:58057433-58057791	IMR90	lung:	n/a	n/a
11	CEBPB	chr1:58058579-58058899	HepG2	liver:	n/a	chr1:58058738-58058749
12	CEBPB	chr1:57954742-57955820	Hela-S3	cervix:	n/a	chr1:57955366-57955377 chr1:57955368-57955377 chr1:57954911-57954924 chr1:57955368-57955377 chr1:57955368-57955377 chr1:57954913-57954924 chr1:57955368-57955377 chr1:57954913-57954924 chr1:57955366-57955379
13	CEBPB	chr1:57976548-57976826	HepG2	liver:	n/a	chr1:57976662-57976673
14	CEBPB	chr1:58058628-58058865	K562	blood:	n/a	chr1:58058738-58058749
15	CEBPB	chr1:57964204-57964368	H1-hESC	embryonic stem cell:	n/a	chr1:57964306-57964317
16	CEBPB	chr1:58057454-58057785	HepG2	liver:	n/a	n/a
17	CEBPB	chr1:57954905-57955722	IMR90	lung:	n/a	chr1:57955366-57955377 chr1:57955368-57955377 chr1:57954911-57954924 chr1:57955368-57955377 chr1:57955368-57955377 chr1:57954913-57954924 chr1:57955368-57955377 chr1:57954913-57954924 chr1:57955366-57955379
18	CEBPB	chr1:58012370-58012559	HepG2	liver:	n/a	chr1:58012453-58012464 chr1:58012499-58012510
19	CEBPB	chr1:58012315-58012513	A549	lung:	n/a	chr1:58012453-58012464 chr1:58012499-58012510
20	CEBPB	chr1:57958734-57959091	IMR90	lung:	n/a	chr1:57958898-57958909
21	CEBPB	chr1:58102752-58103114	IMR90	lung:	n/a	chr1:58102869-58102880
22	CEBPB	chr1:58015040-58015473	HepG2	liver:	n/a	chr1:58015360-58015373 chr1:58015442-58015454 chr1:58015362-58015371 chr1:58015361-58015372
23	CEBPB	chr1:58057416-58057954	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr1:58082341-58082590	HepG2	liver:	n/a	chr1:58082424-58082435 chr1:58082394-58082407
25	CEBPB	chr1:57964159-57964487	IMR90	lung:	n/a	chr1:57964306-57964317
26	CEBPB	chr1:58087547-58087831	HepG2	liver:	n/a	chr1:58087680-58087691 chr1:58087679-58087692 chr1:58087678-58087695
27	CEBPB	chr1:57991186-57991261	HepG2	liver:	n/a	n/a
28	CEBPB	chr1:57969096-57969182	HepG2	liver:	n/a	chr1:57969122-57969133
29	CEBPB	chr1:58058603-58058831	A549	lung:	n/a	chr1:58058738-58058749
30	CEBPB	chr1:57976555-57976776	IMR90	lung:	n/a	chr1:57976662-57976673
31	CEBPB	chr1:57958748-57959054	HepG2	liver:	n/a	chr1:57958898-57958909
32	CEBPB	chr1:57958843-57958944	K562	blood:	n/a	chr1:57958898-57958909
33	CEBPB	chr1:58082349-58082548	A549	lung:	n/a	chr1:58082424-58082435 chr1:58082394-58082407
34	CEBPB	chr1:58058567-58058891	IMR90	lung:	n/a	chr1:58058738-58058749
35	CEBPB	chr1:57983289-57984755	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr1:57964148-57964425	HepG2	liver:	n/a	chr1:57964306-57964317
37	CEBPB	chr1:58017302-58017439	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD2	chr1:57983714-57984672	Hela-S3	cervix:	n/a	n/a
39	CHD2	chr1:58012774-58012833	GM12878	blood:	n/a	n/a
40	CTBP2	chr1:58065752-58066522	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr1:58103204-58103267	Fibrobl	skin:	n/a	n/a
42	CTCF	chr1:58095315-58095551	GM12878	blood:	n/a	n/a
43	CTCF	chr1:57985240-57985390	GM06990	blood:	n/a	n/a
44	CTCF	chr1:58102920-58103070	HPAF	blood vessel:	n/a	n/a
45	CTCF	chr1:57985140-57985290	GM12878	blood:	n/a	n/a
46	CTCF	chr1:58089280-58089430	HepG2	liver:	n/a	n/a
47	CTCF	chr1:57985180-57985330	GM12865	blood:	n/a	n/a
48	CTCF	chr1:58088810-58088852	Fibrobl	skin:	n/a	n/a
49	CTCF	chr1:57955140-57955290	HBMEC	blood vessel:	n/a	n/a
50	CTCF	chr1:57985140-57985290	GM12867	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:58089001-58089051	GM06990	blood:	n/a
2	chr1:58089001-58089051	GM06990	blood:	n/a
3	chr1:57955106-57955156	NT2-D1	testis:	n/a
4	chr1:57998740-57998790	AG04450	lung:	fetal
5	chr1:58089001-58089051	MCF10A-Er-Src	breast:	n/a
6	chr1:58089357-58089407	AG04449	skin:	fetal
7	chr1:57955106-57955156	NHDF-neo	bronchial:	n/a
8	chr1:58063953-58064003	GM19239	blood:	n/a
9	chr1:57955106-57955156	Hepatocyte	liver:	n/a
10	chr1:57983368-57983418	AoSMC	blood vessel:	n/a
11	chr1:57955106-57955156	ovcar-3	ovarian:	n/a
12	chr1:58063953-58064003	SK-N-SH	brain:	n/a
13	chr1:58018699-58018749	Jurkat	blood:	n/a
14	chr1:58089357-58089407	NHDF-neo	bronchial:	n/a
15	chr1:58098908-58098958	GM12878	blood:	n/a
16	chr1:58018699-58018749	GM12891	blood:	n/a
17	chr1:58063953-58064003	SK-N-SH_RA	brain:	n/a
18	chr1:58018699-58018749	PANC-1	pancreas:	n/a
19	chr1:58089357-58089407	SAEC	small airway:	n/a
20	chr1:58089001-58089051	NB4	blood:	n/a
21	chr1:57998740-57998790	HCF	heart:	n/a
22	chr1:58089357-58089407	A549	lung:	n/a
23	chr1:58098908-58098958	SK-N-SH_RA	brain:	n/a
24	chr1:57998740-57998790	AoSMC	blood vessel:	n/a
25	chr1:58018699-58018749	Hepatocyte	liver:	n/a
26	chr1:57955106-57955156	PANC-1	pancreas:	n/a
27	chr1:57983368-57983418	T-47D	breast:	n/a
28	chr1:58098908-58098958	ECC-1	luminal epithelium:	n/a
29	chr1:58098908-58098958	NH-A	brain:	n/a
30	chr1:57983368-57983418	AG09319	gingival:	n/a
31	chr1:58089357-58089407	HIPEpiC	eye:	n/a
32	chr1:58018699-58018749	LNCaP	prostate:	n/a
33	chr1:58089357-58089407	RPTEC	kidney:	n/a
34	chr1:58098908-58098958	PFSK-1	brain:	n/a
35	chr1:58089357-58089407	H1-hESC	embryonic stem cell:	embryo
36	chr1:57998740-57998790	HRCEpiC	kidney:	n/a
37	chr1:58018699-58018749	HPAEpiC	pulmonary alveolar:	n/a
38	chr1:58098908-58098958	HEK293	kidney:	embryo
39	chr1:58098908-58098958	HepG2	liver:	n/a
40	chr1:57983368-57983418	AG04450	lung:	fetal
41	chr1:57998740-57998790	Hepatocyte	liver:	n/a
42	chr1:57998740-57998790	HEEpiC	esophagus:	n/a
43	chr1:57983368-57983418	H1-hESC	embryonic stem cell:	embryo
44	chr1:58089001-58089051	ProgFib	skin:	n/a
45	chr1:58089001-58089051	GM12892	blood:	n/a
46	chr1:57998740-57998790	PFSK-1	brain:	n/a
47	chr1:57983368-57983418	K562	blood:	n/a
48	chr1:57955106-57955156	HepG2	liver:	n/a
49	chr1:58063953-58064003	AG10803	skin:	n/a
50	chr1:57998740-57998790	NB4	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:57957161..57959249-chr1:57964483..57967237,2	K562	blood:
2	chr1:57972252..57973978-chr1:58083473..58085053,2	K562	blood:
3	chr1:57957161..57959249-chr1:57964483..57967237,2	K562	blood:
4	chr1:57972252..57973978-chr1:58083473..58085053,2	K562	blood:
5	chr1:58083604..58085124-chr19:54704799..54707163,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C8A-7	chr1:58098854-58099132	ucscGeneNc_uc001cyv_1
2	lnc-C8A-7	chr1:58100716-58101374	ucscGeneNc_uc001cyv_1
3	lnc-C8B-3	chr1:58071519-58071878	NONHSAT003477

Variant related genes	Relation type
RPS20P5	TF binding region
RPS20P5	CpG island
ENSG00000170889	chromatin interactions

Extended variants
information (count: 5196 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:5196 , 50 per page) page: 1 2 3 4 5 6 7 ... 104

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs570613058	chr1:57950381-57950382	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs115366391	chr1:57950391-57950392	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs77921522	chr1:57950405-57950406	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs553564664	chr1:57950492-57950493	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs6679102	chr1:57950556-57950557	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs560734397	chr1:57950558-57950559	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs573836808	chr1:57950570-57950571	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs139147406	chr1:57950577-57950578	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs145273865	chr1:57950596-57950597	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs183912635	chr1:57950601-57950602	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs114844207	chr1:57950658-57950659	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs115684833	chr1:57950661-57950662	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs565603860	chr1:57950664-57950665	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs188697972	chr1:57950697-57950698	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs531213925	chr1:57950718-57950719	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs144139164	chr1:57950842-57950843	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs200943248	chr1:57950850-57950851	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs147356513	chr1:57950851-57950852	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs146528809	chr1:57950852-57950853	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs60375797	chr1:57950859-57950860	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs192076719	chr1:57950948-57950949	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs567853888	chr1:57950954-57950955	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs115838839	chr1:57950968-57950969	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs546636862	chr1:57951023-57951024	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs184340686	chr1:57951031-57951032	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs375957308	chr1:57951045-57951046	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs538602446	chr1:57951046-57951047	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs111789181	chr1:57951087-57951088	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs558247122	chr1:57951146-57951147	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs575189564	chr1:57951148-57951149	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs1524710	chr1:57951149-57951150	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs554563761	chr1:57951178-57951179	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs373214793	chr1:57951206-57951207	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs554345576	chr1:57951208-57951209	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs574252831	chr1:57951209-57951210	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs541747759	chr1:57951235-57951236	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs542769244	chr1:57951273-57951274	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs559769235	chr1:57951313-57951314	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs190469712	chr1:57951325-57951326	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs545417442	chr1:57951334-57951335	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs182181370	chr1:57951395-57951396	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs531276301	chr1:57951396-57951397	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs79427710	chr1:57951442-57951443	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs2805878	chr1:57951580-57951581	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs59727725	chr1:57951588-57951589	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs57951998	chr1:57951592-57951593	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs111483251	chr1:57951631-57951632	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs566590693	chr1:57951691-57951692	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs532094911	chr1:57951778-57951779	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs375580002	chr1:57951807-57951808	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Papillary thyroid carcinoma	21436994	CNVD
Adenoid cystic carcinoma	18698036	CNVD
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
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
Meckel-Gruber syndrome	21572526	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	16616336	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Breast cancer	21509527	CNVD
Myelofibrosis	22110671	CNVD
Developmental delay	19490664	CNVD
Glioblastoma multiforme	22286061	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	22522925	CNVD
small cell lung cancer	20016488	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Developmental delay	21147756	CNVD

Chromatin state (count:775 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:57940800-57954800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr1:57943200-57955200	Weak transcription	Stomach Mucosa	stomach
3	chr1:57949600-57950800	Weak transcription	Hela-S3	cervix
4	chr1:57949600-57952200	Enhancers	NHDF-Ad	bronchial
5	chr1:57949800-57951000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr1:57949800-57951200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr1:57949800-57951200	Weak transcription	NH-A	brain
8	chr1:57949800-57954600	Weak transcription	NHEK	skin
9	chr1:57950000-57950400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr1:57950000-57951200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr1:57950000-57951200	Weak transcription	NHLF	lung
12	chr1:57950400-57951800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr1:57950800-57952400	Enhancers	Hela-S3	cervix
14	chr1:57951000-57952200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr1:57951200-57951600	Enhancers	Muscle Satellite Cultured Cells	--
16	chr1:57951200-57951800	Enhancers	Osteobl	bone
17	chr1:57951200-57952000	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr1:57951200-57952000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr1:57951200-57952200	Enhancers	NH-A	brain
20	chr1:57951200-57952200	Enhancers	NHLF	lung
21	chr1:57951200-57953200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr1:57951600-57952200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr1:57951600-57954800	Weak transcription	Muscle Satellite Cultured Cells	--
24	chr1:57951800-57954600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr1:57951800-57954800	Weak transcription	Osteobl	bone
26	chr1:57952000-57954800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr1:57952000-57955200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr1:57952200-57954600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr1:57952200-57954600	Weak transcription	NHDF-Ad	bronchial
30	chr1:57952200-57954600	Weak transcription	NHLF	lung
31	chr1:57952200-57954800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr1:57952200-57954800	Weak transcription	NH-A	brain
33	chr1:57952400-57954600	Weak transcription	Hela-S3	cervix
34	chr1:57952800-57953200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr1:57953200-57954600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr1:57953200-57955200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr1:57954600-57955800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr1:57954600-57955800	Enhancers	HSMM	muscle
39	chr1:57954600-57955800	Enhancers	NHEK	skin
40	chr1:57954600-57956000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr1:57954600-57956000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr1:57954600-57956000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr1:57954600-57956000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr1:57954600-57956000	Enhancers	Hela-S3	cervix
45	chr1:57954600-57956000	Enhancers	NHLF	lung
46	chr1:57954600-57956200	Enhancers	NHDF-Ad	bronchial
47	chr1:57954800-57955200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr1:57954800-57955200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr1:57954800-57955400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr1:57954800-57955800	Enhancers	ES-WA7 Cell Line	embryonic stem cell

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