Variant report

Variant	nsv1005022
Chromosome Location	chr1:79950774-80106902
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	CCNT2	chr1:80083401-80083601	K562	blood:	n/a	n/a
4	CEBPB	chr1:80058424-80058771	IMR90	lung:	n/a	chr1:80058589-80058598 chr1:80058589-80058598 chr1:80058589-80058598 chr1:80058587-80058598 chr1:80058586-80058603
5	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
6	CEBPB	chr1:80069577-80069934	HepG2	liver:	n/a	n/a
7	CEBPB	chr1:80034087-80034479	MCF-7	breast:	n/a	chr1:80034307-80034318
8	CEBPB	chr1:79952498-79952690	A549	lung:	n/a	n/a
9	CEBPB	chr1:80069558-80069931	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr1:80058423-80058747	A549	lung:	n/a	chr1:80058589-80058598 chr1:80058589-80058598 chr1:80058589-80058598 chr1:80058587-80058598 chr1:80058586-80058603
11	CEBPB	chr1:80058406-80058767	HepG2	liver:	n/a	chr1:80058589-80058598 chr1:80058589-80058598 chr1:80058589-80058598 chr1:80058587-80058598 chr1:80058586-80058603
12	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
13	CEBPB	chr1:80079851-80080113	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr1:80099132-80099470	IMR90	lung:	n/a	n/a
15	CEBPB	chr1:79966804-79967221	IMR90	lung:	n/a	chr1:79967028-79967037 chr1:79967026-79967039 chr1:79967028-79967037 chr1:79967027-79967038 chr1:79967028-79967037
16	CEBPB	chr1:80030851-80030965	HepG2	liver:	n/a	n/a
17	CEBPB	chr1:80069514-80069965	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr1:80079833-80080160	ECC-1	luminal epithelium:	n/a	n/a
19	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
20	CEBPB	chr1:80094504-80094783	IMR90	lung:	n/a	n/a
21	CEBPB	chr1:79966776-79967231	Hela-S3	cervix:	n/a	chr1:79967028-79967037 chr1:79967026-79967039 chr1:79967028-79967037 chr1:79967027-79967038 chr1:79967028-79967037
22	CEBPB	chr1:80034012-80034595	MCF-7	breast:	n/a	chr1:80034307-80034318
23	CEBPB	chr1:79966861-79967129	MCF-7	breast:	n/a	chr1:79967028-79967037 chr1:79967026-79967039 chr1:79967028-79967037 chr1:79967027-79967038 chr1:79967028-79967037
24	CEBPB	chr1:80069551-80069937	IMR90	lung:	n/a	n/a
25	CEBPB	chr1:80034129-80034419	HepG2	liver:	n/a	chr1:80034307-80034318
26	CEBPB	chr1:80058447-80058756	Hela-S3	cervix:	n/a	chr1:80058589-80058598 chr1:80058589-80058598 chr1:80058589-80058598 chr1:80058587-80058598 chr1:80058586-80058603
27	CEBPB	chr1:80069532-80069923	ECC-1	luminal epithelium:	n/a	n/a
28	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
29	CEBPB	chr1:80079811-80080169	IMR90	lung:	n/a	n/a
30	CEBPB	chr1:79966863-79967171	K562	blood:	n/a	chr1:79967028-79967037 chr1:79967026-79967039 chr1:79967028-79967037 chr1:79967027-79967038 chr1:79967028-79967037
31	CEBPB	chr1:80069530-80070001	MCF-7	breast:	n/a	n/a
32	CEBPB	chr1:80069632-80069919	A549	lung:	n/a	n/a
33	CEBPB	chr1:80069572-80069986	MCF-7	breast:	n/a	n/a
34	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
35	CEBPB	chr1:80079815-80080149	HepG2	liver:	n/a	n/a
36	CEBPB	chr1:79998520-79998617	A549	lung:	n/a	chr1:79998597-79998610 chr1:79998599-79998610
37	CEBPB	chr1:79966805-79967217	HepG2	liver:	n/a	chr1:79967028-79967037 chr1:79967026-79967039 chr1:79967028-79967037 chr1:79967027-79967038 chr1:79967028-79967037
38	CEBPB	chr1:80069617-80069952	ECC-1	luminal epithelium:	n/a	n/a
39	CEBPB	chr1:79976191-79976311	A549	lung:	n/a	n/a
40	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
41	CEBPB	chr1:80079827-80080176	A549	lung:	n/a	n/a
42	CEBPB	chr1:80079808-80080186	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr1:80034120-80034494	IMR90	lung:	n/a	chr1:80034307-80034318
44	CEBPB	chr1:79966859-79967219	A549	lung:	n/a	chr1:79967028-79967037 chr1:79967026-79967039 chr1:79967028-79967037 chr1:79967027-79967038 chr1:79967028-79967037
45	CREB1	chr1:79985043-79985496	GM12878	blood:	n/a	n/a
46	CTCF	chr1:80083580-80083730	HCM	heart:	n/a	n/a
47	CTCF	chr1:80083540-80083690	SK-N-SH_RA	brain:	n/a	n/a
48	CTCF	chr1:79962980-79963130	NB4	blood:	n/a	n/a
49	CTCF	chr1:79963000-79963150	GM12878	blood:	n/a	n/a
50	CTCF	chr1:80083520-80083670	Hela-S3	cervix:	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	H1-hESC	embryonic stem cell:	embryo
3	chr1:80069752-80069802	PANC-1	pancreas:	n/a
4	chr1:80069752-80069802	NT2-D1	testis:	n/a
5	chr1:79961576-79961626	PFSK-1	brain:	n/a
6	chr1:79961576-79961626	HRE	kidney:	n/a
7	chr1:80069752-80069802	SK-N-SH	brain:	n/a
8	chr1:79961576-79961626	HRPEpiC	eye:	n/a
9	chr1:79961576-79961626	HCF	heart:	n/a
10	chr1:80069752-80069802	RPTEC	kidney:	n/a
11	chr1:79961576-79961626	SK-N-SH	brain:	n/a
12	chr1:79961576-79961626	NHDF-neo	bronchial:	n/a
13	chr1:79961576-79961626	HEK293	kidney:	embryo
14	chr1:79961576-79961626	HUVEC	blood vessel:	n/a
15	chr1:79961576-79961626	GM12892	blood:	n/a
16	chr1:80069752-80069802	AG09319	gingival:	n/a
17	chr1:80069752-80069802	HCF	heart:	n/a
18	chr1:79961576-79961626	SK-N-MC	brain:	n/a
19	chr1:80069752-80069802	PFSK-1	brain:	n/a
20	chr1:79961576-79961626	AG04450	lung:	fetal
21	chr1:80069752-80069802	K562	blood:	n/a
22	chr1:79961576-79961626	GM12878	blood:	n/a
23	chr1:80069752-80069802	LNCaP	prostate:	n/a
24	chr1:80069752-80069802	HNPCEpiC	eye:	n/a
25	chr1:79961576-79961626	HCM	heart:	n/a
26	chr1:80069752-80069802	AG10803	skin:	n/a
27	chr1:79961576-79961626	HEEpiC	esophagus:	n/a
28	chr1:79961576-79961626	HCPEpiC	choroid plexus:	n/a
29	chr1:79961576-79961626	AG10803	skin:	n/a
30	chr1:79961576-79961626	HL-60	blood:	n/a
31	chr1:80069752-80069802	GM12892	blood:	n/a
32	chr1:79961576-79961626	Caco-2	colon:	n/a
33	chr1:80069752-80069802	GM19239	blood:	n/a
34	chr1:80069752-80069802	Caco-2	colon:	n/a
35	chr1:80069752-80069802	ProgFib	skin:	n/a
36	chr1:80069752-80069802	HMEC	breast:	n/a
37	chr1:80069752-80069802	AG09309	skin:	n/a
38	chr1:79961576-79961626	GM19239	blood:	n/a
39	chr1:80069752-80069802	HepG2	liver:	n/a
40	chr1:80069752-80069802	NHBE	bronchial:	n/a
41	chr1:79961576-79961626	MCF10A-Er-Src	breast:	n/a
42	chr1:79961576-79961626	K562	blood:	n/a
43	chr1:80069752-80069802	PrEC	prostate:	n/a
44	chr1:79961576-79961626	HMEC	breast:	n/a
45	chr1:79961576-79961626	A549	lung:	n/a
46	chr1:79961576-79961626	NH-A	brain:	n/a
47	chr1:80069752-80069802	HCT-116	colon:	n/a
48	chr1:80069752-80069802	Hepatocyte	liver:	n/a
49	chr1:80069752-80069802	NHDF-neo	bronchial:	n/a
50	chr1:79961576-79961626	SKMC	muscle:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:79967863..79970281-chr1:79971191..79972711,2	K562	blood:
2	chr1:80078496..80080442-chr1:80082313..80085209,2	K562	blood:
3	chr1:80047758..80050486-chr1:80050910..80053801,2	MCF-7	breast:
4	chr1:80078496..80080442-chr1:80082313..80085209,2	K562	blood:
5	chr1:79967863..79970281-chr1:79971191..79972711,2	K562	blood:
6	chr1:80026893..80029713-chr1:80030293..80033252,2	K562	blood:
7	chr1:80091538..80094295-chr1:80099191..80102045,2	K562	blood:
8	chr1:79901761..79904453-chr1:79988728..79990739,2	K562	blood:
9	chr1:78468665..78470165-chr1:80026349..80029039,2	K562	blood:
10	chr1:80098711..80101528-chr1:80111688..80113709,2	K562	blood:
11	chr1:80047758..80050486-chr1:80050910..80053801,2	MCF-7	breast:
12	chr1:80026893..80029713-chr1:80030293..80033252,2	K562	blood:
13	chr1:79962962..79963539-chr1:80683583..80684326,2	MCF-7	breast:
14	chr1:80091538..80094295-chr1:80099191..80102045,2	K562	blood:
15	chr1:80048884..80051726-chr1:80174478..80177354,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ELTD1-10	chr1:79959246-79959486	NONHSAT004101

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

Extended variants
information (count: 2832 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:2832 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs151236020	chr1:79950794-79950795	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs574937328	chr1:79950812-79950813	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs17418410	chr1:79950828-79950829	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs560399304	chr1:79950877-79950878	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs527652401	chr1:79950911-79950912	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs17103256	chr1:79950913-79950914	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs564173905	chr1:79950928-79950929	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs541312798	chr1:79950983-79950984	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs561165975	chr1:79950987-79950988	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs531491773	chr1:79950998-79950999	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs368174276	chr1:79951025-79951026	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs538030343	chr1:79951029-79951030	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs140532858	chr1:79951037-79951038	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs530195388	chr1:79951048-79951049	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs12045663	chr1:79951049-79951050	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs368722625	chr1:79951052-79951053	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs145672994	chr1:79951085-79951086	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs4604653	chr1:79951103-79951104	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs61767601	chr1:79951136-79951137	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs185933037	chr1:79951247-79951248	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs531303556	chr1:79951269-79951270	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs555232880	chr1:79951277-79951278	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs199891962	chr1:79951280-79951281	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs10874038	chr1:79951289-79951290	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs576156428	chr1:79951293-79951294	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs138353740	chr1:79951296-79951297	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs1494843	chr1:79951308-79951309	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs574943695	chr1:79951314-79951315	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs191642396	chr1:79951330-79951331	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs74866094	chr1:79951336-79951337	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs547687387	chr1:79951379-79951380	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs572191458	chr1:79951393-79951394	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs545932595	chr1:79951401-79951402	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs567486215	chr1:79951404-79951405	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs564137078	chr1:79951445-79951446	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs536406802	chr1:79951454-79951455	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs183936749	chr1:79951496-79951497	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs187316002	chr1:79951534-79951535	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs529055679	chr1:79951564-79951565	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs190961381	chr1:79951609-79951610	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs570181156	chr1:79951614-79951615	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs538750321	chr1:79951725-79951726	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs182720323	chr1:79951727-79951728	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs533058550	chr1:79951835-79951836	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs541470935	chr1:79951859-79951860	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs551504090	chr1:79951882-79951883	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs2934868	chr1:79951886-79951887	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs537061656	chr1:79951921-79951922	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs572087962	chr1:79951937-79951938	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs556790982	chr1:79952008-79952009	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	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:232 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:79943600-79951200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr1:79943800-79951400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr1:79944200-79951400	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr1:79946800-79951400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr1:79949200-79951600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr1:79949400-79950800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr1:79949400-79951800	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr1:79949400-79952000	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr1:79950000-79952000	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr1:79950200-79950800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
11	chr1:79950600-79951000	Enhancers	H1 Cell Line	embryonic stem cell
12	chr1:79950600-79951800	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr1:79950800-79951800	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr1:79951000-79951400	Weak transcription	H1 Cell Line	embryonic stem cell
15	chr1:79951200-79951400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
16	chr1:79951400-79951600	Enhancers	H1 Cell Line	embryonic stem cell
17	chr1:79951400-79951800	Enhancers	H9 Cell Line	embryonic stem cell
18	chr1:79951400-79951800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr1:79951400-79952200	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr1:79951600-79960400	Weak transcription	H1 Cell Line	embryonic stem cell
21	chr1:79951800-79953600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
22	chr1:79951800-79953800	Weak transcription	HUES48 Cell Line	embryonic stem cell
23	chr1:79951800-79954000	Weak transcription	HUES6 Cell Line	embryonic stem cell
24	chr1:79952000-79953200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
25	chr1:79952000-79954200	Weak transcription	HUES64 Cell Line	embryonic stem cell
26	chr1:79952200-79953000	Genic enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr1:79953000-79953800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr1:79953200-79953800	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr1:79953600-79954200	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr1:79953800-79954000	Genic enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr1:79953800-79954000	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
32	chr1:79953800-79955000	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr1:79953800-79955000	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr1:79954000-79954400	Transcr. at gene 5' and 3'	ES-I3 Cell Line	embryonic stem cell
35	chr1:79954000-79954400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr1:79954000-79954400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
37	chr1:79954000-79955000	Active TSS	iPS-15b Cell Line	embryonic stem cell
38	chr1:79954200-79954400	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr1:79954400-79954800	Weak transcription	HUES64 Cell Line	embryonic stem cell
40	chr1:79954400-79955000	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr1:79954400-79955400	Active TSS	ES-I3 Cell Line	embryonic stem cell
42	chr1:79954400-79956400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr1:79954800-79955000	Enhancers	HUES64 Cell Line	embryonic stem cell
44	chr1:79955000-79956200	Weak transcription	HUES6 Cell Line	embryonic stem cell
45	chr1:79955000-79956200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
46	chr1:79955000-79958600	Weak transcription	HUES64 Cell Line	embryonic stem cell
47	chr1:79955000-79958800	Weak transcription	HUES48 Cell Line	embryonic stem cell
48	chr1:79955400-79956400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
49	chr1:79956200-79960000	Active TSS	HUES6 Cell Line	embryonic stem cell
50	chr1:79956200-79960000	Active TSS	iPS-15b Cell Line	embryonic stem cell

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