Variant report

Variant	nsv437210
Chromosome Location	chr1:62419727-62448245
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	ATF3	chr1:62433476-62433726	K562	blood:	n/a	n/a
2	BACH1	chr1:62446381-62446560	K562	blood:	n/a	n/a
3	BACH1	chr1:62446282-62446790	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr1:62437864-62437982	K562	blood:	n/a	n/a
5	CEBPB	chr1:62440045-62440224	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr1:62446295-62446907	K562	blood:	n/a	chr1:62446734-62446745 chr1:62446733-62446746 chr1:62446733-62446746
7	CEBPB	chr1:62446583-62446870	HepG2	liver:	n/a	chr1:62446734-62446745 chr1:62446733-62446746 chr1:62446733-62446746
8	CEBPB	chr1:62440023-62440267	HepG2	liver:	n/a	n/a
9	CEBPB	chr1:62440045-62440218	K562	blood:	n/a	n/a
10	CEBPB	chr1:62446313-62446586	K562	blood:	n/a	n/a
11	CEBPB	chr1:62446324-62446874	H1-hESC	embryonic stem cell:	n/a	chr1:62446734-62446745 chr1:62446733-62446746 chr1:62446733-62446746
12	CEBPB	chr1:62446355-62446912	IMR90	lung:	n/a	chr1:62446734-62446745 chr1:62446733-62446746 chr1:62446733-62446746
13	CEBPB	chr1:62432189-62432433	H1-hESC	embryonic stem cell:	n/a	n/a
14	CHD2	chr1:62446418-62446581	H1-hESC	embryonic stem cell:	n/a	n/a
15	CHD2	chr1:62448125-62448179	GM12878	blood:	n/a	n/a
16	CTCF	chr1:62440228-62440270	Kidney_OC	kidney:	n/a	n/a
17	CTCF	chr1:62426894-62426915	Kidney_OC	kidney:	n/a	n/a
18	CTCF	chr1:62446374-62446425	Fibrobl	skin:	n/a	n/a
19	CUX1	chr1:62433241-62433259	K562	blood:	n/a	n/a
20	E2F4	chr1:62440236-62440368	MCF10A-Er-Src	breast:	n/a	n/a
21	E2F4	chr1:62438634-62439009	MCF10A-Er-Src	breast:	n/a	n/a
22	E2F4	chr1:62446465-62446664	MCF10A-Er-Src	breast:	n/a	chr1:62446509-62446518
23	EP300	chr1:62433418-62433730	SK-N-SH_RA	brain:	n/a	chr1:62433649-62433657 chr1:62433655-62433664 chr1:62433702-62433716 chr1:62433479-62433493
24	EP300	chr1:62432611-62432792	K562	blood:	n/a	n/a
25	EP300	chr1:62433430-62433743	SK-N-SH_RA	brain:	n/a	chr1:62433649-62433657 chr1:62433655-62433664 chr1:62433702-62433716 chr1:62433479-62433493
26	ESR1	chr1:62432481-62432805	T-47D	breast:	n/a	n/a
27	ESR1	chr1:62432573-62432749	T-47D	breast:	n/a	n/a
28	FOS	chr1:62446306-62446560	MCF10A-Er-Src	breast:	n/a	chr1:62446463-62446475 chr1:62446464-62446474
29	FOS	chr1:62446306-62446593	MCF10A-Er-Src	breast:	n/a	chr1:62446463-62446475 chr1:62446464-62446474
30	FOS	chr1:62440032-62440239	MCF10A-Er-Src	breast:	n/a	n/a
31	FOS	chr1:62438816-62439128	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr1:62421968-62422017	MCF10A-Er-Src	breast:	n/a	chr1:62421972-62421982 chr1:62422005-62422017 chr1:62421972-62421982
33	FOS	chr1:62446297-62446593	MCF10A-Er-Src	breast:	n/a	chr1:62446463-62446475 chr1:62446464-62446474
34	FOS	chr1:62440039-62440275	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr1:62438769-62439219	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr1:62440074-62440275	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr1:62440055-62440275	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr1:62446342-62446638	MCF10A-Er-Src	breast:	n/a	chr1:62446463-62446475 chr1:62446464-62446474
39	FOS	chr1:62438813-62439128	MCF10A-Er-Src	breast:	n/a	n/a
40	FOXA1	chr1:62441344-62441639	T-47D	breast:	n/a	n/a
41	FOXA1	chr1:62426877-62427059	ECC-1	luminal epithelium:	n/a	n/a
42	FOXA1	chr1:62441400-62441592	T-47D	breast:	n/a	n/a
43	FOXP2	chr1:62446307-62446517	SK-N-MC	brain:	n/a	n/a
44	GATA2	chr1:62445408-62445710	K562	blood:	n/a	n/a
45	GATA2	chr1:62433432-62433718	SH-SY5Y	brain:	n/a	n/a
46	GATA3	chr1:62433139-62433695	SH-SY5Y	brain:	n/a	chr1:62433143-62433150 chr1:62433141-62433150 chr1:62433143-62433150 chr1:62433141-62433151 chr1:62433143-62433150
47	GATA3	chr1:62448112-62448183	SH-SY5Y	brain:	n/a	n/a
48	GATA3	chr1:62433236-62433904	SK-N-SH	brain:	n/a	n/a
49	GATA3	chr1:62441311-62441758	T-47D	breast:	n/a	n/a
50	GATA3	chr1:62432959-62433967	SK-N-SH	brain:	n/a	chr1:62433143-62433150 chr1:62433141-62433150 chr1:62433143-62433150 chr1:62433136-62433157 chr1:62433138-62433154 chr1:62433141-62433151 chr1:62433143-62433150

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:62445916-62445966	NHDF-neo	bronchial:	n/a
2	chr1:62445916-62445966	MCF-7	breast:	n/a
3	chr1:62445916-62445966	BJ	skin:	n/a
4	chr1:62445916-62445966	H1-hESC	embryonic stem cell:	embryo
5	chr1:62445916-62445966	NT2-D1	testis:	n/a
6	chr1:62445916-62445966	GM12891	blood:	n/a
7	chr1:62445916-62445966	HNPCEpiC	eye:	n/a
8	chr1:62445916-62445966	ECC-1	luminal epithelium:	n/a
9	chr1:62445916-62445966	HRE	kidney:	n/a
10	chr1:62445916-62445966	LNCaP	prostate:	n/a
11	chr1:62445916-62445966	AG09319	gingival:	n/a
12	chr1:62445916-62445966	MCF10A-Er-Src	breast:	n/a
13	chr1:62445916-62445966	HepG2	liver:	n/a
14	chr1:62445916-62445966	HL-60	blood:	n/a
15	chr1:62445916-62445966	HEEpiC	esophagus:	n/a
16	chr1:62445916-62445966	PANC-1	pancreas:	n/a
17	chr1:62445916-62445966	HPAEpiC	pulmonary alveolar:	n/a
18	chr1:62445916-62445966	BE2_C	brain:	n/a
19	chr1:62445916-62445966	AG09309	skin:	n/a
20	chr1:62445916-62445966	AG10803	skin:	n/a
21	chr1:62445916-62445966	NB4	blood:	n/a
22	chr1:62445916-62445966	NH-A	brain:	n/a
23	chr1:62445916-62445966	HEK293	kidney:	embryo
24	chr1:62445916-62445966	SK-N-SH	brain:	n/a
25	chr1:62445916-62445966	SK-N-MC	brain:	n/a
26	chr1:62445916-62445966	NHBE	bronchial:	n/a
27	chr1:62445916-62445966	HCT-116	colon:	n/a
28	chr1:62445916-62445966	K562	blood:	n/a
29	chr1:62445916-62445966	AG04449	skin:	fetal
30	chr1:62445916-62445966	PFSK-1	brain:	n/a
31	chr1:62445916-62445966	A549	lung:	n/a
32	chr1:62445916-62445966	Hepatocyte	liver:	n/a
33	chr1:62445916-62445966	HAEpiC	amniotic membrane:	n/a
34	chr1:62445916-62445966	AoSMC	blood vessel:	n/a
35	chr1:62445916-62445966	HIPEpiC	eye:	n/a
36	chr1:62445916-62445966	T-47D	breast:	n/a
37	chr1:62445916-62445966	SKMC	muscle:	n/a
38	chr1:62445916-62445966	CMK	blood:	n/a
39	chr1:62445916-62445966	GM12892	blood:	n/a
40	chr1:62445916-62445966	Hela-S3	cervix:	n/a
41	chr1:62445916-62445966	Caco-2	colon:	n/a
42	chr1:62445916-62445966	Jurkat	blood:	n/a
43	chr1:62445916-62445966	GM12878	blood:	n/a
44	chr1:62445916-62445966	HCF	heart:	n/a
45	chr1:62445916-62445966	GM06990	blood:	n/a
46	chr1:62445916-62445966	HRCEpiC	kidney:	n/a
47	chr1:62445916-62445966	SK-N-SH_RA	brain:	n/a
48	chr1:62445916-62445966	RPTEC	kidney:	n/a
49	chr1:62445916-62445966	HMEC	breast:	n/a
50	chr1:62445916-62445966	HRPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:62420887..62422924-chr1:62423218..62424749,2	MCF-7	breast:
2	chr1:62420887..62422924-chr1:62423218..62424749,2	MCF-7	breast:
3	chr1:62444307..62446951-chr1:62447722..62450460,2	K562	blood:
4	chr1:62417324..62419162-chr1:62419469..62421904,2	MCF-7	breast:
5	chr1:62444307..62446951-chr1:62447722..62450460,2	K562	blood:

Variant related genes	Relation type
INADL	TF binding region
INADL	CpG island
ENSG00000132849	chromatin interactions

Extended variants
information (count: 1008 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:1008 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3737108	chr1:62419727-62419728	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs565083170	chr1:62419760-62419761	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs575790807	chr1:62419788-62419789	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs564689642	chr1:62419806-62419807	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs56304307	chr1:62419881-62419882	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs79889387	chr1:62419888-62419889	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs547682715	chr1:62419889-62419890	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs190925207	chr1:62419906-62419907	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs566328633	chr1:62419907-62419908	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs138555913	chr1:62419917-62419918	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs548359815	chr1:62419942-62419943	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs570260609	chr1:62419947-62419948	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs149233230	chr1:62419998-62419999	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs559026698	chr1:62420030-62420031	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs116058605	chr1:62420289-62420290	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs2151124	chr1:62420303-62420304	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs180880989	chr1:62420341-62420342	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs572354551	chr1:62420373-62420374	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs542970227	chr1:62420379-62420380	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs560890751	chr1:62420384-62420385	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs373997284	chr1:62420424-62420425	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs202123341	chr1:62420426-62420427	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs147592633	chr1:62420427-62420428	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs576198665	chr1:62420456-62420457	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs546101214	chr1:62420460-62420461	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs543108414	chr1:62420503-62420504	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs564993536	chr1:62420536-62420537	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs2498961	chr1:62420550-62420551	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs11809259	chr1:62420586-62420587	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs558960707	chr1:62420606-62420607	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs530309957	chr1:62420664-62420665	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs143340410	chr1:62420666-62420667	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs147543666	chr1:62420671-62420672	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs570117003	chr1:62420674-62420675	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs537661426	chr1:62420677-62420678	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs11587923	chr1:62420723-62420724	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs187231687	chr1:62420808-62420809	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs7418394	chr1:62420972-62420973	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs7418404	chr1:62421010-62421011	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs140067286	chr1:62421019-62421020	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs535156535	chr1:62421022-62421023	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs145600340	chr1:62421024-62421025	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs576871219	chr1:62421033-62421034	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs534779136	chr1:62421145-62421146	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs7538041	chr1:62421171-62421172	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs116774615	chr1:62421229-62421230	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs139784772	chr1:62421305-62421306	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs561781486	chr1:62421395-62421396	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs558514339	chr1:62421397-62421398	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs576516988	chr1:62421423-62421424	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:95)

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
Breast cancer	16620391	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Breast cancer	17133270	CNVD
Myelofibrosis	22110671	CNVD
CNS Malformation Syndrome	17530927	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Colorectal cancer	20459617	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:241 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:62350600-62428200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
2	chr1:62385000-62494200	Weak transcription	Aorta	Aorta
3	chr1:62393800-62422400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr1:62406600-62430200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr1:62409000-62436800	Weak transcription	Primary T helper cells PMA-I stimulated	--
6	chr1:62409200-62456000	Weak transcription	Rectal Mucosa Donor 31	rectum
7	chr1:62409200-62456800	Weak transcription	Rectal Mucosa Donor 29	rectum
8	chr1:62409200-62457000	Weak transcription	Fetal Intestine Large	intestine
9	chr1:62409200-62518600	Weak transcription	Pancreas	Pancrea
10	chr1:62409400-62429600	Weak transcription	Gastric	stomach
11	chr1:62409400-62458400	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr1:62410200-62425200	Weak transcription	Fetal Intestine Small	intestine
13	chr1:62416600-62420000	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr1:62416800-62426800	Weak transcription	HepG2	liver
15	chr1:62417400-62419800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr1:62417600-62421800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr1:62417800-62419800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr1:62417800-62431600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr1:62418000-62428800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr1:62418200-62419800	Enhancers	H1 Cell Line	embryonic stem cell
21	chr1:62418200-62420800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr1:62418200-62421000	Weak transcription	Psoas Muscle	Psoas
23	chr1:62418200-62421800	Weak transcription	H9 Cell Line	embryonic stem cell
24	chr1:62418200-62446400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr1:62418400-62419800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr1:62418400-62420000	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr1:62418400-62421600	Weak transcription	Skeletal Muscle Female	skeletal muscle
28	chr1:62418400-62441400	Weak transcription	Fetal Kidney	kidney
29	chr1:62418600-62420000	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr1:62418600-62420200	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr1:62418600-62432400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr1:62418600-62432400	Weak transcription	NHEK	skin
33	chr1:62418800-62421800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr1:62418800-62422800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr1:62418800-62432800	Weak transcription	HMEC	breast
36	chr1:62419200-62420400	Enhancers	iPS-20b Cell Line	embryonic stem cell
37	chr1:62419200-62424400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
38	chr1:62419400-62421800	Weak transcription	HUES6 Cell Line	embryonic stem cell
39	chr1:62419600-62419800	Enhancers	Skeletal Muscle Male	skeletal muscle
40	chr1:62419600-62421400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
41	chr1:62419600-62421800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
42	chr1:62419600-62426800	Weak transcription	Right Atrium	heart
43	chr1:62419600-62445800	Weak transcription	Left Ventricle	heart
44	chr1:62419800-62421800	Weak transcription	H1 Cell Line	embryonic stem cell
45	chr1:62419800-62422200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr1:62420000-62421600	Weak transcription	HUES64 Cell Line	embryonic stem cell
47	chr1:62420000-62422000	Weak transcription	HUES48 Cell Line	embryonic stem cell
48	chr1:62420000-62422200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
49	chr1:62420200-62422000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
50	chr1:62420400-62421400	Weak transcription	iPS-20b Cell Line	embryonic stem cell

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