Variant report

Variant	nsv470720
Chromosome Location	chr1:79411764-79491206
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	BACH1	chr1:79472315-79472519	H1-hESC	embryonic stem cell:	n/a	n/a
2	BRCA1	chr1:79415111-79415262	Hela-S3	cervix:	n/a	n/a
3	BRCA1	chr1:79459804-79459831	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr1:79490003-79490203	A549	lung:	n/a	chr1:79490066-79490077
5	CEBPB	chr1:79451150-79451399	K562	blood:	n/a	chr1:79451261-79451272 chr1:79451259-79451270 chr1:79451259-79451272 chr1:79451201-79451214
6	CEBPB	chr1:79451090-79451446	IMR90	lung:	n/a	chr1:79451261-79451272 chr1:79451259-79451270 chr1:79451259-79451272 chr1:79451201-79451214
7	CEBPB	chr1:79470712-79470946	A549	lung:	n/a	chr1:79470789-79470800
8	CEBPB	chr1:79451113-79451392	HepG2	liver:	n/a	chr1:79451261-79451272 chr1:79451259-79451270 chr1:79451259-79451272 chr1:79451201-79451214
9	CEBPB	chr1:79453639-79453775	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr1:79470706-79470922	Hela-S3	cervix:	n/a	chr1:79470789-79470800
11	CEBPB	chr1:79489957-79490304	HepG2	liver:	n/a	chr1:79490066-79490077
12	CEBPB	chr1:79483498-79483817	HepG2	liver:	n/a	chr1:79483669-79483680
13	CEBPB	chr1:79414890-79415047	HepG2	liver:	n/a	chr1:79414944-79414957 chr1:79414973-79414990
14	CEBPB	chr1:79414781-79415272	Hela-S3	cervix:	n/a	chr1:79414944-79414957 chr1:79414973-79414990
15	CEBPB	chr1:79482686-79482859	HepG2	liver:	n/a	chr1:79482727-79482740 chr1:79482727-79482738 chr1:79482727-79482740
16	CEBPB	chr1:79451152-79451394	A549	lung:	n/a	chr1:79451261-79451272 chr1:79451259-79451270 chr1:79451259-79451272 chr1:79451201-79451214
17	CEBPB	chr1:79490048-79490150	H1-hESC	embryonic stem cell:	n/a	chr1:79490066-79490077
18	CEBPB	chr1:79470648-79470928	HepG2	liver:	n/a	chr1:79470789-79470800
19	CTBP2	chr1:79472140-79472635	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr1:79465180-79465330	GM06990	blood:	n/a	n/a
21	CTCF	chr1:79489620-79489770	NHLF	lung:	n/a	n/a
22	CTCF	chr1:79438660-79438692	Lung_OC	lung:	n/a	n/a
23	CTCF	chr1:79429600-79429750	GM06990	blood:	n/a	n/a
24	CTCF	chr1:79472560-79472710	HCM	heart:	n/a	n/a
25	CTCF	chr1:79433023-79433073	GM13976	blood:	n/a	n/a
26	CTCF	chr1:79424140-79424290	NHLF	lung:	n/a	n/a
27	EP300	chr1:79414914-79415277	Hela-S3	cervix:	n/a	n/a
28	FOS	chr1:79472161-79473325	HUVEC	blood vessel:	n/a	chr1:79472502-79472513
29	FOS	chr1:79462522-79462737	MCF10A-Er-Src	breast:	n/a	chr1:79462637-79462646
30	FOS	chr1:79418474-79418595	MCF10A-Er-Src	breast:	n/a	chr1:79418556-79418567 chr1:79418558-79418569 chr1:79418558-79418570 chr1:79418560-79418568
31	FOS	chr1:79462544-79462663	MCF10A-Er-Src	breast:	n/a	chr1:79462637-79462646
32	FOS	chr1:79418400-79418657	HUVEC	blood vessel:	n/a	chr1:79418556-79418567 chr1:79418558-79418569 chr1:79418558-79418570 chr1:79418560-79418568
33	FOS	chr1:79462513-79462750	MCF10A-Er-Src	breast:	n/a	chr1:79462637-79462646
34	FOXA1	chr1:79433972-79434376	HepG2	liver:	n/a	n/a
35	GATA2	chr1:79476344-79476570	HUVEC	blood vessel:	n/a	chr1:79476435-79476442 chr1:79476427-79476441
36	GATA2	chr1:79415034-79415289	HUVEC	blood vessel:	n/a	chr1:79415105-79415114 chr1:79415070-79415086 chr1:79415117-79415125 chr1:79415102-79415112 chr1:79415098-79415119 chr1:79415192-79415204 chr1:79415105-79415112
37	GATA2	chr1:79471774-79472669	HUVEC	blood vessel:	n/a	chr1:79472502-79472511 chr1:79471827-79471837 chr1:79471828-79471840 chr1:79471826-79471842
38	GATA3	chr1:79482818-79482964	SH-SY5Y	brain:	n/a	chr1:79482933-79482949
39	GATA3	chr1:79488643-79489167	SK-N-SH	brain:	n/a	n/a
40	GATA3	chr1:79470027-79470161	SH-SY5Y	brain:	n/a	chr1:79470111-79470118
41	GATA3	chr1:79428630-79428828	SH-SY5Y	brain:	n/a	n/a
42	GATA3	chr1:79416972-79417460	SK-N-SH	brain:	n/a	n/a
43	GATA3	chr1:79457757-79457977	SH-SY5Y	brain:	n/a	chr1:79457818-79457831
44	GATA3	chr1:79456602-79457241	SH-SY5Y	brain:	n/a	chr1:79456989-79457006
45	GATA3	chr1:79476344-79476544	SH-SY5Y	brain:	n/a	chr1:79476435-79476442
46	GATA3	chr1:79416880-79417437	SK-N-SH	brain:	n/a	n/a
47	GTF2F1	chr1:79472324-79472486	H1-hESC	embryonic stem cell:	n/a	n/a
48	IRF1	chr1:79443191-79443269	K562	blood:	n/a	n/a
49	JUN	chr1:79472406-79472596	H1-hESC	embryonic stem cell:	n/a	chr1:79472502-79472513
50	JUN	chr1:79471610-79471967	HUVEC	blood vessel:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:79472532-79472582	CMK	blood:	n/a
2	chr1:79472532-79472582	CMK	blood:	n/a
3	chr1:79472917-79472967	HRCEpiC	kidney:	n/a
4	chr1:79472917-79472967	Caco-2	colon:	n/a
5	chr1:79472558-79472608	HL-60	blood:	n/a
6	chr1:79472536-79472586	GM12892	blood:	n/a
7	chr1:79474718-79474768	ovcar-3	ovarian:	n/a
8	chr1:79472532-79472582	GM19239	blood:	n/a
9	chr1:79472536-79472586	GM12891	blood:	n/a
10	chr1:79473783-79473833	GM06990	blood:	n/a
11	chr1:79472917-79472967	PANC-1	pancreas:	n/a
12	chr1:79472558-79472608	AoSMC	blood vessel:	n/a
13	chr1:79471984-79472034	BJ	skin:	n/a
14	chr1:79472452-79472502	SK-N-MC	brain:	n/a
15	chr1:79472408-79472458	HCPEpiC	choroid plexus:	n/a
16	chr1:79472558-79472608	GM12878	blood:	n/a
17	chr1:79474718-79474768	HCT-116	colon:	n/a
18	chr1:79472643-79472693	AoSMC	blood vessel:	n/a
19	chr1:79473783-79473833	AoSMC	blood vessel:	n/a
20	chr1:79472643-79472693	HepG2	liver:	n/a
21	chr1:79472532-79472582	GM06990	blood:	n/a
22	chr1:79474718-79474768	BE2_C	brain:	n/a
23	chr1:79472282-79472332	SAEC	small airway:	n/a
24	chr1:79472408-79472458	HepG2	liver:	n/a
25	chr1:79474718-79474768	HNPCEpiC	eye:	n/a
26	chr1:79472361-79472411	GM19239	blood:	n/a
27	chr1:79472917-79472967	HRE	kidney:	n/a
28	chr1:79472643-79472693	Hela-S3	cervix:	n/a
29	chr1:79471984-79472034	Jurkat	blood:	n/a
30	chr1:79472558-79472608	NB4	blood:	n/a
31	chr1:79472536-79472586	Hepatocyte	liver:	n/a
32	chr1:79471984-79472034	ProgFib	skin:	n/a
33	chr1:79472643-79472693	GM12891	blood:	n/a
34	chr1:79474718-79474768	GM12892	blood:	n/a
35	chr1:79472536-79472586	GM06990	blood:	n/a
36	chr1:79472532-79472582	HCT-116	colon:	n/a
37	chr1:79472558-79472608	SAEC	small airway:	n/a
38	chr1:79472282-79472332	CMK	blood:	n/a
39	chr1:79472343-79472393	GM12892	blood:	n/a
40	chr1:79472917-79472967	SAEC	small airway:	n/a
41	chr1:79472361-79472411	PANC-1	pancreas:	n/a
42	chr1:79473783-79473833	K562	blood:	n/a
43	chr1:79472536-79472586	AG09309	skin:	n/a
44	chr1:79473783-79473833	PFSK-1	brain:	n/a
45	chr1:79472361-79472411	AG10803	skin:	n/a
46	chr1:79472408-79472458	MCF10A-Er-Src	breast:	n/a
47	chr1:79472643-79472693	HCM	heart:	n/a
48	chr1:79472452-79472502	HNPCEpiC	eye:	n/a
49	chr1:79473783-79473833	HRPEpiC	eye:	n/a
50	chr1:79472361-79472411	AG04450	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr1:79411840..79414575-chr1:79858123..79860401,2	K562	blood:
2	chr1:79484446..79486654-chr1:79486860..79488839,2	MCF-7	breast:
3	chr1:79410821..79413576-chr1:79414533..79416679,2	K562	blood:
4	chr1:79484446..79486654-chr1:79486860..79488839,2	MCF-7	breast:
5	chr1:79410821..79413576-chr1:79414533..79416679,2	K562	blood:
6	chr1:79370114..79372345-chr1:79443530..79445892,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ELTD1-2	chr1:79490858-79491009	XLOC_000877

Variant related genes	Relation type
ELTD1	TF binding region
ELTD1	CpG island
IGSF1	miRNA target sites

Extended variants
information (count: 2770 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:2770 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2035725	chr1:79411764-79411765	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs80233432	chr1:79411820-79411821	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs2035724	chr1:79411828-79411829	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs554387628	chr1:79411857-79411858	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs572715866	chr1:79411858-79411859	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs372474121	chr1:79411866-79411867	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs546525515	chr1:79411868-79411869	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs723898	chr1:79411888-79411889	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs369215955	chr1:79411894-79411895	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs576655507	chr1:79411910-79411911	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs6675156	chr1:79411918-79411919	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs373493278	chr1:79411928-79411929	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs200539312	chr1:79411950-79411951	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs11162579	chr1:79411951-79411952	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs541091913	chr1:79411961-79411962	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs41313381	chr1:79411968-79411969	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs532915062	chr1:79412020-79412021	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs117741748	chr1:79412041-79412042	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs200973848	chr1:79412068-79412069	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs185392778	chr1:79412096-79412097	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs199976603	chr1:79412099-79412100	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs528123910	chr1:79412104-79412105	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs376613673	chr1:79412111-79412112	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs370778799	chr1:79412114-79412115	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs569313723	chr1:79412159-79412160	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs76695428	chr1:79412163-79412164	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs530698298	chr1:79412175-79412176	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs12752044	chr1:79412207-79412208	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs567120141	chr1:79412213-79412214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs534720862	chr1:79412227-79412228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs553060670	chr1:79412250-79412251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs11162580	chr1:79412289-79412290	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs372405517	chr1:79412303-79412304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs12405700	chr1:79412322-79412323	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs75721048	chr1:79412349-79412350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs182246476	chr1:79412357-79412358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs187296244	chr1:79412360-79412361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs34556678	chr1:79412398-79412399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs12409126	chr1:79412408-79412409	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs17102491	chr1:79412442-79412443	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs541130355	chr1:79412485-79412486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs189651260	chr1:79412497-79412498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs533240805	chr1:79412506-79412507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs180906295	chr1:79412552-79412553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs563314263	chr1:79412606-79412607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs17102494	chr1:79412612-79412613	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs185660120	chr1:79412650-79412651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs190365706	chr1:79412774-79412775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs76411649	chr1:79412776-79412777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs546611559	chr1:79412810-79412811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

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
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:231 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:79409800-79412200	Strong transcription	HUVEC	blood vessel
2	chr1:79410200-79414800	Weak transcription	Hela-S3	cervix
3	chr1:79412200-79418400	Weak transcription	HUVEC	blood vessel
4	chr1:79413000-79418400	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr1:79414800-79415000	Enhancers	Pancreatic Islets	Pancreatic Islet
6	chr1:79414800-79419400	Enhancers	Hela-S3	cervix
7	chr1:79416200-79417000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr1:79416600-79417000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr1:79417000-79431400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr1:79418400-79418800	Enhancers	Muscle Satellite Cultured Cells	--
11	chr1:79418400-79419600	Enhancers	HUVEC	blood vessel
12	chr1:79419600-79429200	Weak transcription	HUVEC	blood vessel
13	chr1:79424200-79424600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr1:79426400-79426600	Active TSS	Gastric	stomach
15	chr1:79426600-79432000	Weak transcription	Gastric	stomach
16	chr1:79429200-79429800	Strong transcription	HUVEC	blood vessel
17	chr1:79429800-79431800	Weak transcription	HUVEC	blood vessel
18	chr1:79431400-79431800	Weak transcription	Muscle Satellite Cultured Cells	--
19	chr1:79431400-79434000	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr1:79431400-79436000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr1:79431800-79432200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
22	chr1:79431800-79432400	ZNF genes & repeats	Muscle Satellite Cultured Cells	--
23	chr1:79431800-79432400	ZNF genes & repeats	Left Ventricle	heart
24	chr1:79431800-79432600	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr1:79431800-79433000	ZNF genes & repeats	HUVEC	blood vessel
26	chr1:79431800-79433200	ZNF genes & repeats	Adipose Nuclei	Adipose
27	chr1:79432000-79432400	ZNF genes & repeats	Gastric	stomach
28	chr1:79432000-79432400	ZNF genes & repeats	Osteobl	bone
29	chr1:79432200-79432400	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr1:79432200-79432400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
31	chr1:79432400-79433400	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
32	chr1:79432400-79436000	Weak transcription	Osteobl	bone
33	chr1:79433000-79433800	Strong transcription	HUVEC	blood vessel
34	chr1:79433800-79443800	Weak transcription	HUVEC	blood vessel
35	chr1:79434000-79447800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr1:79436000-79437200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr1:79436200-79437400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr1:79437200-79445600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr1:79437400-79438200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr1:79438400-79438600	Enhancers	H1 Cell Line	embryonic stem cell
41	chr1:79438400-79439000	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr1:79438600-79438800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
43	chr1:79443800-79446000	Strong transcription	HUVEC	blood vessel
44	chr1:79445600-79445800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr1:79445800-79446400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr1:79445800-79446800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr1:79445800-79446800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
48	chr1:79445800-79446800	Enhancers	Osteobl	bone
49	chr1:79446000-79448600	Weak transcription	HUVEC	blood vessel
50	chr1:79446400-79446600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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