Variant report

Variant	nsv546636
Chromosome Location	chr1:79964823-80079996
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	chr1:79985055-79985451	GM12878	blood:	n/a	n/a
2	ATF2	chr1:79985113-79985414	GM12878	blood:	n/a	n/a
3	CEBPB	chr1:80058424-80058771	IMR90	lung:	n/a	chr1:80058589-80058598 chr1:80058589-80058598 chr1:80058589-80058598 chr1:80058587-80058598 chr1:80058586-80058603
4	CEBPB	chr1:79966861-79967129	MCF-7	breast:	n/a	chr1:79967028-79967037 chr1:79967026-79967039 chr1:79967028-79967037 chr1:79967027-79967038 chr1:79967028-79967037
5	CEBPB	chr1:79966804-79967221	IMR90	lung:	n/a	chr1:79967028-79967037 chr1:79967026-79967039 chr1:79967028-79967037 chr1:79967027-79967038 chr1:79967028-79967037
6	CEBPB	chr1:80034129-80034419	HepG2	liver:	n/a	chr1:80034307-80034318
7	CEBPB	chr1:80069551-80069937	IMR90	lung:	n/a	n/a
8	CEBPB	chr1:80058447-80058756	Hela-S3	cervix:	n/a	chr1:80058589-80058598 chr1:80058589-80058598 chr1:80058589-80058598 chr1:80058587-80058598 chr1:80058586-80058603
9	CEBPB	chr1:80069514-80069965	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr1:79976191-79976311	A549	lung:	n/a	n/a
11	CEBPB	chr1:80079815-80080149	HepG2	liver:	n/a	n/a
12	CEBPB	chr1:80034120-80034494	IMR90	lung:	n/a	chr1:80034307-80034318
13	CEBPB	chr1:80069532-80069923	ECC-1	luminal epithelium:	n/a	n/a
14	CEBPB	chr1:79966857-79967179	H1-hESC	embryonic stem cell:	n/a	chr1:79967028-79967037 chr1:79967026-79967039 chr1:79967028-79967037 chr1:79967027-79967038 chr1:79967028-79967037
15	CEBPB	chr1:79966800-79967193	ECC-1	luminal epithelium:	n/a	chr1:79967028-79967037 chr1:79967026-79967039 chr1:79967028-79967037 chr1:79967027-79967038 chr1:79967028-79967037
16	CEBPB	chr1:80079808-80080186	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr1:80069632-80069919	A549	lung:	n/a	n/a
18	CEBPB	chr1:80034087-80034479	MCF-7	breast:	n/a	chr1:80034307-80034318
19	CEBPB	chr1:80069530-80070001	MCF-7	breast:	n/a	n/a
20	CEBPB	chr1:80058423-80058747	A549	lung:	n/a	chr1:80058589-80058598 chr1:80058589-80058598 chr1:80058589-80058598 chr1:80058587-80058598 chr1:80058586-80058603
21	CEBPB	chr1:80069572-80069986	MCF-7	breast:	n/a	n/a
22	CEBPB	chr1:80079833-80080160	ECC-1	luminal epithelium:	n/a	n/a
23	CEBPB	chr1:80069558-80069931	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr1:80079827-80080176	A549	lung:	n/a	n/a
25	CEBPB	chr1:80034012-80034595	MCF-7	breast:	n/a	chr1:80034307-80034318
26	CEBPB	chr1:80069617-80069952	ECC-1	luminal epithelium:	n/a	n/a
27	CEBPB	chr1:80058395-80058748	ECC-1	luminal epithelium:	n/a	chr1:80058589-80058598 chr1:80058589-80058598 chr1:80058589-80058598 chr1:80058587-80058598 chr1:80058586-80058603
28	CEBPB	chr1:80079851-80080113	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr1:79966863-79967171	K562	blood:	n/a	chr1:79967028-79967037 chr1:79967026-79967039 chr1:79967028-79967037 chr1:79967027-79967038 chr1:79967028-79967037
30	CEBPB	chr1:79998520-79998617	A549	lung:	n/a	chr1:79998597-79998610 chr1:79998599-79998610
31	CEBPB	chr1:79966887-79967286	A549	lung:	n/a	chr1:79967028-79967037 chr1:79967229-79967241 chr1:79967026-79967039 chr1:79967028-79967037 chr1:79967027-79967038 chr1:79967028-79967037
32	CEBPB	chr1:79966828-79967239	ECC-1	luminal epithelium:	n/a	chr1:79967028-79967037 chr1:79967026-79967039 chr1:79967028-79967037 chr1:79967027-79967038 chr1:79967028-79967037
33	CEBPB	chr1:80079811-80080169	IMR90	lung:	n/a	n/a
34	CEBPB	chr1:80058406-80058767	HepG2	liver:	n/a	chr1:80058589-80058598 chr1:80058589-80058598 chr1:80058589-80058598 chr1:80058587-80058598 chr1:80058586-80058603
35	CEBPB	chr1:79966776-79967231	Hela-S3	cervix:	n/a	chr1:79967028-79967037 chr1:79967026-79967039 chr1:79967028-79967037 chr1:79967027-79967038 chr1:79967028-79967037
36	CEBPB	chr1:80058429-80058770	H1-hESC	embryonic stem cell:	n/a	chr1:80058589-80058598 chr1:80058589-80058598 chr1:80058589-80058598 chr1:80058587-80058598 chr1:80058586-80058603
37	CEBPB	chr1:80030851-80030965	HepG2	liver:	n/a	n/a
38	CEBPB	chr1:79966859-79967219	A549	lung:	n/a	chr1:79967028-79967037 chr1:79967026-79967039 chr1:79967028-79967037 chr1:79967027-79967038 chr1:79967028-79967037
39	CEBPB	chr1:79966805-79967217	HepG2	liver:	n/a	chr1:79967028-79967037 chr1:79967026-79967039 chr1:79967028-79967037 chr1:79967027-79967038 chr1:79967028-79967037
40	CEBPB	chr1:80069577-80069934	HepG2	liver:	n/a	n/a
41	CREB1	chr1:79985043-79985496	GM12878	blood:	n/a	n/a
42	CTCF	chr1:80059645-80059671	LNCaP	prostate:	n/a	n/a
43	CTCF	chr1:80053020-80053170	AoAF	blood vessel:	n/a	chr1:80053100-80053121
44	CTCF	chr1:80060106-80060156	Lung_OC	lung:	n/a	n/a
45	CTCF	chr1:80022020-80022170	GM12872	blood:	n/a	n/a
46	CTCF	chr1:80053085-80053128	GM13977	blood:	n/a	chr1:80053100-80053121
47	CTCF	chr1:79973500-79973650	RPTEC	kidney:	n/a	n/a
48	CTCF	chr1:80021980-80022130	HPAF	blood vessel:	n/a	n/a
49	CTCF	chr1:80028508-80028546	Lung_OC	lung:	n/a	n/a
50	CTCF	chr1:79986778-79986814	ProgFib	skin:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:80069752-80069802	HAEpiC	amniotic membrane:	n/a
2	chr1:80069752-80069802	AG09309	skin:	n/a
3	chr1:80069752-80069802	ProgFib	skin:	n/a
4	chr1:80069752-80069802	HEEpiC	esophagus:	n/a
5	chr1:80069752-80069802	NHDF-neo	bronchial:	n/a
6	chr1:80069752-80069802	PrEC	prostate:	n/a
7	chr1:80069752-80069802	NT2-D1	testis:	n/a
8	chr1:80069752-80069802	GM12878	blood:	n/a
9	chr1:80069752-80069802	HCF	heart:	n/a
10	chr1:80069752-80069802	Hepatocyte	liver:	n/a
11	chr1:80069752-80069802	T-47D	breast:	n/a
12	chr1:80069752-80069802	RPTEC	kidney:	n/a
13	chr1:80069752-80069802	HRPEpiC	eye:	n/a
14	chr1:80069752-80069802	ECC-1	luminal epithelium:	n/a
15	chr1:80069752-80069802	HRE	kidney:	n/a
16	chr1:80069752-80069802	HMEC	breast:	n/a
17	chr1:80069752-80069802	BE2_C	brain:	n/a
18	chr1:80069752-80069802	HIPEpiC	eye:	n/a
19	chr1:80069752-80069802	CMK	blood:	n/a
20	chr1:80069752-80069802	A549	lung:	n/a
21	chr1:80069752-80069802	PANC-1	pancreas:	n/a
22	chr1:80069752-80069802	HepG2	liver:	n/a
23	chr1:80069752-80069802	AG10803	skin:	n/a
24	chr1:80069752-80069802	NB4	blood:	n/a
25	chr1:80069752-80069802	SK-N-MC	brain:	n/a
26	chr1:80069752-80069802	HRCEpiC	kidney:	n/a
27	chr1:80069752-80069802	SAEC	small airway:	n/a
28	chr1:80069752-80069802	SK-N-SH_RA	brain:	n/a
29	chr1:80069752-80069802	MCF10A-Er-Src	breast:	n/a
30	chr1:80069752-80069802	HCPEpiC	choroid plexus:	n/a
31	chr1:80069752-80069802	Hela-S3	cervix:	n/a
32	chr1:80069752-80069802	AG04450	lung:	fetal
33	chr1:80069752-80069802	ovcar-3	ovarian:	n/a
34	chr1:80069752-80069802	HCT-116	colon:	n/a
35	chr1:80069752-80069802	IMR90	lung:	fetal
36	chr1:80069752-80069802	HUVEC	blood vessel:	n/a
37	chr1:80069752-80069802	AG04449	skin:	fetal
38	chr1:80069752-80069802	GM06990	blood:	n/a
39	chr1:80069752-80069802	H1-hESC	embryonic stem cell:	embryo
40	chr1:80069752-80069802	HNPCEpiC	eye:	n/a
41	chr1:80069752-80069802	GM19239	blood:	n/a
42	chr1:80069752-80069802	BJ	skin:	n/a
43	chr1:80069752-80069802	K562	blood:	n/a
44	chr1:80069752-80069802	SK-N-SH	brain:	n/a
45	chr1:80069752-80069802	Jurkat	blood:	n/a
46	chr1:80069752-80069802	HL-60	blood:	n/a
47	chr1:80069752-80069802	Caco-2	colon:	n/a
48	chr1:80069752-80069802	SKMC	muscle:	n/a
49	chr1:80069752-80069802	AG09319	gingival:	n/a
50	chr1:80069752-80069802	HEK293	kidney:	embryo

No.	Distal block	Cell Line	Cell type
1	chr1:78468665..78470165-chr1:80026349..80029039,2	K562	blood:
2	chr1:79967863..79970281-chr1:79971191..79972711,2	K562	blood:
3	chr1:79967863..79970281-chr1:79971191..79972711,2	K562	blood:
4	chr1:80078496..80080442-chr1:80082313..80085209,2	K562	blood:
5	chr1:80026893..80029713-chr1:80030293..80033252,2	K562	blood:
6	chr1:79901761..79904453-chr1:79988728..79990739,2	K562	blood:
7	chr1:80048884..80051726-chr1:80174478..80177354,2	K562	blood:
8	chr1:80047758..80050486-chr1:80050910..80053801,2	MCF-7	breast:
9	chr1:80047758..80050486-chr1:80050910..80053801,2	MCF-7	breast:
10	chr1:80026893..80029713-chr1:80030293..80033252,2	K562	blood:

Variant related genes	Relation type
ADH5P2	TF binding region
ADH5P2	CpG island

Extended variants
information (count: 1663 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:1663 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1389944	chr1:79964823-79964824	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs571436880	chr1:79964864-79964865	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs531477615	chr1:79964901-79964902	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs17418579	chr1:79964919-79964920	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs145225055	chr1:79964920-79964921	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs148244921	chr1:79965036-79965037	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs536908164	chr1:79965067-79965068	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs573952237	chr1:79965075-79965076	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs372859517	chr1:79965080-79965081	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs201623732	chr1:79965085-79965086	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs566924520	chr1:79965089-79965090	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs534380996	chr1:79965110-79965111	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs558921350	chr1:79965111-79965112	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs143995329	chr1:79965114-79965115	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs79552933	chr1:79965183-79965184	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs181171159	chr1:79965200-79965201	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs12140075	chr1:79965229-79965230	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs574507126	chr1:79965244-79965245	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs528376544	chr1:79965252-79965253	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs72680398	chr1:79965262-79965263	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs554010793	chr1:79965285-79965286	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs184284644	chr1:79965310-79965311	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs545967131	chr1:79965314-79965315	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs564323173	chr1:79965315-79965316	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs531390152	chr1:79965393-79965394	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs1494856	chr1:79965429-79965430	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs561634377	chr1:79965455-79965456	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs1494855	chr1:79965499-79965500	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs547104906	chr1:79965500-79965501	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs74095894	chr1:79965569-79965570	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs142203584	chr1:79965579-79965580	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs552691551	chr1:79965604-79965605	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs537092621	chr1:79965666-79965667	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs77992011	chr1:79965676-79965677	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs537913872	chr1:79965695-79965696	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs1494854	chr1:79965760-79965761	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs201429652	chr1:79965769-79965770	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs568239839	chr1:79965771-79965772	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs545275190	chr1:79965807-79965808	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs535824683	chr1:79965816-79965817	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs553917208	chr1:79966081-79966082	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs572304092	chr1:79966084-79966085	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs545784207	chr1:79966101-79966102	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs368379162	chr1:79966121-79966122	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs565158958	chr1:79966142-79966143	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs189016584	chr1:79966186-79966187	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs576322262	chr1:79966209-79966210	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs543515925	chr1:79966211-79966212	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs527707336	chr1:79966229-79966230	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs12044896	chr1:79966232-79966233	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:102)

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
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16774939	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:79961800-79968000	Weak transcription	HUES6 Cell Line	embryonic stem cell
2	chr1:79962800-79965000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr1:79963200-79967600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr1:79964400-79965600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr1:79964400-79966600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr1:79964400-79966800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr1:79964800-79965000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr1:79965000-79965400	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr1:79965200-79966200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr1:79965400-79966600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr1:79966200-79966600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr1:79966600-79967000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr1:79966600-79968600	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr1:79966800-79968000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr1:79967000-79967200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr1:79967200-79970000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr1:79968000-79968200	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr1:79968000-79968200	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr1:79968000-79968400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr1:79968400-79968600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr1:79968400-79969800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr1:79970000-79970200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr1:79970200-79970400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr1:79970200-79973200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr1:79973200-79974000	Enhancers	Primary T cells from cord blood	blood
26	chr1:79973200-79974400	Enhancers	Liver	Liver
27	chr1:79973600-79973800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr1:79981800-79982000	Enhancers	Fetal Thymus	thymus
29	chr1:79983000-79985200	Enhancers	Primary T cells from cord blood	blood
30	chr1:79983200-79984600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr1:79983400-79983800	Enhancers	Liver	Liver
32	chr1:79983600-79984000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr1:79984400-79985400	Enhancers	GM12878-XiMat	blood
34	chr1:79995400-79996400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr1:80011800-80012200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr1:80014400-80015400	Enhancers	Fetal Muscle Leg	muscle
37	chr1:80015400-80016600	Weak transcription	Fetal Muscle Leg	muscle
38	chr1:80016800-80017000	Enhancers	Fetal Muscle Leg	muscle
39	chr1:80020400-80021000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr1:80027000-80027800	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
41	chr1:80038400-80041600	Enhancers	HUVEC	blood vessel
42	chr1:80050200-80051000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
43	chr1:80050400-80050600	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
44	chr1:80050800-80051800	Weak transcription	HUES6 Cell Line	embryonic stem cell
45	chr1:80051400-80054200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
46	chr1:80051600-80052400	Enhancers	Psoas Muscle	Psoas
47	chr1:80051800-80052400	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr1:80052000-80052400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr1:80052000-80052400	Enhancers	HUES6 Cell Line	embryonic stem cell
50	chr1:80052000-80052800	Enhancers	HUES48 Cell Line	embryonic stem cell

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