Variant report

Variant	nsv870769
Chromosome Location	chr1:79420491-79491206
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	chr1:79459804-79459831	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr1:79489957-79490304	HepG2	liver:	n/a	chr1:79490066-79490077
4	CEBPB	chr1:79451150-79451399	K562	blood:	n/a	chr1:79451261-79451272 chr1:79451259-79451270 chr1:79451259-79451272 chr1:79451201-79451214
5	CEBPB	chr1:79483498-79483817	HepG2	liver:	n/a	chr1:79483669-79483680
6	CEBPB	chr1:79490048-79490150	H1-hESC	embryonic stem cell:	n/a	chr1:79490066-79490077
7	CEBPB	chr1:79470648-79470928	HepG2	liver:	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	chr1:79451090-79451446	IMR90	lung:	n/a	chr1:79451261-79451272 chr1:79451259-79451270 chr1:79451259-79451272 chr1:79451201-79451214
10	CEBPB	chr1:79490003-79490203	A549	lung:	n/a	chr1:79490066-79490077
11	CEBPB	chr1:79451152-79451394	A549	lung:	n/a	chr1:79451261-79451272 chr1:79451259-79451270 chr1:79451259-79451272 chr1:79451201-79451214
12	CEBPB	chr1:79482686-79482859	HepG2	liver:	n/a	chr1:79482727-79482740 chr1:79482727-79482738 chr1:79482727-79482740
13	CEBPB	chr1:79470712-79470946	A549	lung:	n/a	chr1:79470789-79470800
14	CEBPB	chr1:79470706-79470922	Hela-S3	cervix:	n/a	chr1:79470789-79470800
15	CEBPB	chr1:79453639-79453775	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTBP2	chr1:79472140-79472635	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr1:79472560-79472710	HCM	heart:	n/a	n/a
18	CTCF	chr1:79424140-79424290	NHLF	lung:	n/a	n/a
19	CTCF	chr1:79429600-79429750	GM06990	blood:	n/a	n/a
20	CTCF	chr1:79438660-79438692	Lung_OC	lung:	n/a	n/a
21	CTCF	chr1:79465180-79465330	GM06990	blood:	n/a	n/a
22	CTCF	chr1:79433023-79433073	GM13976	blood:	n/a	n/a
23	CTCF	chr1:79489620-79489770	NHLF	lung:	n/a	n/a
24	FOS	chr1:79462513-79462750	MCF10A-Er-Src	breast:	n/a	chr1:79462637-79462646
25	FOS	chr1:79462544-79462663	MCF10A-Er-Src	breast:	n/a	chr1:79462637-79462646
26	FOS	chr1:79462522-79462737	MCF10A-Er-Src	breast:	n/a	chr1:79462637-79462646
27	FOS	chr1:79472161-79473325	HUVEC	blood vessel:	n/a	chr1:79472502-79472513
28	FOXA1	chr1:79433972-79434376	HepG2	liver:	n/a	n/a
29	GATA2	chr1:79476344-79476570	HUVEC	blood vessel:	n/a	chr1:79476435-79476442 chr1:79476427-79476441
30	GATA2	chr1:79471774-79472669	HUVEC	blood vessel:	n/a	chr1:79472502-79472511 chr1:79471827-79471837 chr1:79471828-79471840 chr1:79471826-79471842
31	GATA3	chr1:79488643-79489167	SK-N-SH	brain:	n/a	n/a
32	GATA3	chr1:79428630-79428828	SH-SY5Y	brain:	n/a	n/a
33	GATA3	chr1:79456602-79457241	SH-SY5Y	brain:	n/a	chr1:79456989-79457006
34	GATA3	chr1:79470027-79470161	SH-SY5Y	brain:	n/a	chr1:79470111-79470118
35	GATA3	chr1:79476344-79476544	SH-SY5Y	brain:	n/a	chr1:79476435-79476442
36	GATA3	chr1:79457757-79457977	SH-SY5Y	brain:	n/a	chr1:79457818-79457831
37	GATA3	chr1:79482818-79482964	SH-SY5Y	brain:	n/a	chr1:79482933-79482949
38	GTF2F1	chr1:79472324-79472486	H1-hESC	embryonic stem cell:	n/a	n/a
39	IRF1	chr1:79443191-79443269	K562	blood:	n/a	n/a
40	JUN	chr1:79471610-79471967	HUVEC	blood vessel:	n/a	n/a
41	JUN	chr1:79472406-79472596	H1-hESC	embryonic stem cell:	n/a	chr1:79472502-79472513
42	JUND	chr1:79471648-79471969	HepG2	liver:	n/a	n/a
43	KAP1	chr1:79431995-79432315	HEK293	kidney:	n/a	n/a
44	MAFF	chr1:79452876-79453031	HepG2	liver:	n/a	chr1:79452921-79452939
45	MAFF	chr1:79428143-79428425	HepG2	liver:	n/a	chr1:79428303-79428321
46	MAFF	chr1:79490564-79490764	HepG2	liver:	n/a	chr1:79490700-79490718
47	MAFK	chr1:79452798-79453064	IMR90	lung:	n/a	chr1:79452924-79452933 chr1:79452922-79452937 chr1:79452923-79452933
48	MAFK	chr1:79490655-79490700	IMR90	lung:	n/a	n/a
49	MAFK	chr1:79452836-79453048	HepG2	liver:	n/a	chr1:79452924-79452933 chr1:79452922-79452937 chr1:79452923-79452933
50	MAFK	chr1:79490633-79490830	HepG2	liver:	n/a	chr1:79490701-79490717 chr1:79490706-79490717 chr1:79490705-79490716 chr1:79490704-79490718 chr1:79490706-79490717 chr1:79490705-79490716

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:79473783-79473833	HepG2	liver:	n/a
2	chr1:79473783-79473833	HepG2	liver:	n/a
3	chr1:79472408-79472458	NB4	blood:	n/a
4	chr1:79472343-79472393	HAEpiC	amniotic membrane:	n/a
5	chr1:79473783-79473833	HNPCEpiC	eye:	n/a
6	chr1:79472643-79472693	AG04449	skin:	fetal
7	chr1:79472408-79472458	IMR90	lung:	fetal
8	chr1:79472558-79472608	HCM	heart:	n/a
9	chr1:79472361-79472411	HCF	heart:	n/a
10	chr1:79472643-79472693	A549	lung:	n/a
11	chr1:79474718-79474768	GM12891	blood:	n/a
12	chr1:79472532-79472582	Jurkat	blood:	n/a
13	chr1:79474718-79474768	Hepatocyte	liver:	n/a
14	chr1:79472282-79472332	GM12891	blood:	n/a
15	chr1:79472532-79472582	AG10803	skin:	n/a
16	chr1:79473783-79473833	PANC-1	pancreas:	n/a
17	chr1:79471984-79472034	HIPEpiC	eye:	n/a
18	chr1:79473783-79473833	K562	blood:	n/a
19	chr1:79472343-79472393	HCPEpiC	choroid plexus:	n/a
20	chr1:79472643-79472693	ProgFib	skin:	n/a
21	chr1:79472532-79472582	HNPCEpiC	eye:	n/a
22	chr1:79472361-79472411	NB4	blood:	n/a
23	chr1:79472282-79472332	BE2_C	brain:	n/a
24	chr1:79472536-79472586	GM12891	blood:	n/a
25	chr1:79472452-79472502	K562	blood:	n/a
26	chr1:79472917-79472967	SKMC	muscle:	n/a
27	chr1:79472408-79472458	SKMC	muscle:	n/a
28	chr1:79474718-79474768	MCF10A-Er-Src	breast:	n/a
29	chr1:79471984-79472034	HCPEpiC	choroid plexus:	n/a
30	chr1:79474718-79474768	NHDF-neo	bronchial:	n/a
31	chr1:79472361-79472411	HAEpiC	amniotic membrane:	n/a
32	chr1:79472361-79472411	BJ	skin:	n/a
33	chr1:79472536-79472586	RPTEC	kidney:	n/a
34	chr1:79472558-79472608	AG04450	lung:	fetal
35	chr1:79473783-79473833	AoSMC	blood vessel:	n/a
36	chr1:79472917-79472967	HCM	heart:	n/a
37	chr1:79472361-79472411	SKMC	muscle:	n/a
38	chr1:79472343-79472393	ECC-1	luminal epithelium:	n/a
39	chr1:79472917-79472967	HL-60	blood:	n/a
40	chr1:79473783-79473833	A549	lung:	n/a
41	chr1:79472643-79472693	GM12891	blood:	n/a
42	chr1:79472343-79472393	HRPEpiC	eye:	n/a
43	chr1:79472343-79472393	HCT-116	colon:	n/a
44	chr1:79471984-79472034	GM19239	blood:	n/a
45	chr1:79472361-79472411	HRPEpiC	eye:	n/a
46	chr1:79473783-79473833	T-47D	breast:	n/a
47	chr1:79473783-79473833	HUVEC	blood vessel:	n/a
48	chr1:79472343-79472393	HIPEpiC	eye:	n/a
49	chr1:79472532-79472582	ovcar-3	ovarian:	n/a
50	chr1:79472282-79472332	HEK293	kidney:	embryo

No.	Distal block	Cell Line	Cell type
1	chr1:79370114..79372345-chr1:79443530..79445892,2	K562	blood:
2	chr1:79484446..79486654-chr1:79486860..79488839,2	MCF-7	breast:
3	chr1:79484446..79486654-chr1:79486860..79488839,2	MCF-7	breast:

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: 2406 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:2406 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11162581	chr1:79420491-79420492	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs536807197	chr1:79420556-79420557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs548421846	chr1:79420559-79420560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs76553817	chr1:79420584-79420585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs566631030	chr1:79420596-79420597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs112313178	chr1:79420615-79420616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs141267168	chr1:79420626-79420627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs558857740	chr1:79420698-79420699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs1387422	chr1:79420704-79420705	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs78228814	chr1:79420724-79420725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs182739020	chr1:79420858-79420859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs187430161	chr1:79420913-79420914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs541488346	chr1:79420942-79420943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs192179268	chr1:79420982-79420983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs573432555	chr1:79420999-79421000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs184756718	chr1:79421049-79421050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs559866160	chr1:79421058-79421059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs374118742	chr1:79421062-79421063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs528610510	chr1:79421077-79421078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs565608699	chr1:79421113-79421114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs375897814	chr1:79421115-79421116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs542026252	chr1:79421118-79421119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs532673042	chr1:79421173-79421174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs1489390	chr1:79421176-79421177	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs562837842	chr1:79421195-79421196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs188941146	chr1:79421255-79421256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs147081945	chr1:79421275-79421276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs568887810	chr1:79421334-79421335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs192710373	chr1:79421336-79421337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs138089986	chr1:79421342-79421343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs4650621	chr1:79421356-79421357	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs557727245	chr1:79421357-79421358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs552071045	chr1:79421373-79421374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs75122692	chr1:79421400-79421401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs537716310	chr1:79421413-79421414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs184469913	chr1:79421456-79421457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs574053070	chr1:79421470-79421471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs535081178	chr1:79421480-79421481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs375170388	chr1:79421495-79421496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs370968413	chr1:79421521-79421522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs58435051	chr1:79421583-79421584	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs548976662	chr1:79421594-79421595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs189779350	chr1:79421604-79421605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs181147035	chr1:79421696-79421697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs558856539	chr1:79421727-79421728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs367595217	chr1:79421735-79421736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs577482503	chr1:79421793-79421794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs142550471	chr1:79421811-79421812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs562874366	chr1:79421820-79421821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs12568976	chr1:79421840-79421841	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	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:221 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:79417000-79431400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr1:79419600-79429200	Weak transcription	HUVEC	blood vessel
3	chr1:79424200-79424600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr1:79426400-79426600	Active TSS	Gastric	stomach
5	chr1:79426600-79432000	Weak transcription	Gastric	stomach
6	chr1:79429200-79429800	Strong transcription	HUVEC	blood vessel
7	chr1:79429800-79431800	Weak transcription	HUVEC	blood vessel
8	chr1:79431400-79431800	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr1:79431400-79434000	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr1:79431400-79436000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr1:79431800-79432200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
12	chr1:79431800-79432400	ZNF genes & repeats	Muscle Satellite Cultured Cells	--
13	chr1:79431800-79432400	ZNF genes & repeats	Left Ventricle	heart
14	chr1:79431800-79432600	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr1:79431800-79433000	ZNF genes & repeats	HUVEC	blood vessel
16	chr1:79431800-79433200	ZNF genes & repeats	Adipose Nuclei	Adipose
17	chr1:79432000-79432400	ZNF genes & repeats	Gastric	stomach
18	chr1:79432000-79432400	ZNF genes & repeats	Osteobl	bone
19	chr1:79432200-79432400	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr1:79432200-79432400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
21	chr1:79432400-79433400	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
22	chr1:79432400-79436000	Weak transcription	Osteobl	bone
23	chr1:79433000-79433800	Strong transcription	HUVEC	blood vessel
24	chr1:79433800-79443800	Weak transcription	HUVEC	blood vessel
25	chr1:79434000-79447800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr1:79436000-79437200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr1:79436200-79437400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr1:79437200-79445600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr1:79437400-79438200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr1:79438400-79438600	Enhancers	H1 Cell Line	embryonic stem cell
31	chr1:79438400-79439000	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr1:79438600-79438800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
33	chr1:79443800-79446000	Strong transcription	HUVEC	blood vessel
34	chr1:79445600-79445800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr1:79445800-79446400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr1:79445800-79446800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr1:79445800-79446800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
38	chr1:79445800-79446800	Enhancers	Osteobl	bone
39	chr1:79446000-79448600	Weak transcription	HUVEC	blood vessel
40	chr1:79446400-79446600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr1:79446400-79446800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr1:79446800-79447800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
43	chr1:79447800-79448800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
44	chr1:79448600-79448800	Enhancers	HUVEC	blood vessel
45	chr1:79448800-79449000	Genic enhancers	HUVEC	blood vessel
46	chr1:79449000-79451400	Weak transcription	HUVEC	blood vessel
47	chr1:79451400-79452200	Strong transcription	HUVEC	blood vessel
48	chr1:79452200-79455200	Weak transcription	HUVEC	blood vessel
49	chr1:79455200-79466000	Strong transcription	HUVEC	blood vessel
50	chr1:79455400-79460800	Weak transcription	Muscle Satellite Cultured Cells	--

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