Variant report

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10493320	0.95[ASN][1000 genomes]
rs11207957	0.87[ASN][1000 genomes]
rs12058486	0.95[ASN][1000 genomes]
rs12063531	0.95[ASN][1000 genomes]
rs12065844	0.93[ASN][1000 genomes]
rs12078087	0.98[ASN][1000 genomes]
rs12079207	0.95[ASN][1000 genomes]
rs12082238	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12718429	0.95[ASN][1000 genomes]
rs12724349	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12760226	0.93[ASN][1000 genomes]
rs12760895	0.95[ASN][1000 genomes]
rs2296518	0.95[ASN][1000 genomes]
rs2477872	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2666487	0.98[ASN][1000 genomes]
rs2666488	0.98[ASN][1000 genomes]
rs2765258	0.98[ASN][1000 genomes]
rs2765261	0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2765263	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34752481	0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7520614	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs765691	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs765692	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs912894	0.95[ASN][1000 genomes]
rs912895	0.95[ASN][1000 genomes]
rs912896	0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1004446	chr1:62394631-62813533	Enhancers ZNF genes & repeats Weak transcription Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	12 gene(s)	inside rSNPs	diseases
2	nsv534984	chr1:62394631-62813533	Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	12 gene(s)	inside rSNPs	diseases
3	nsv1009398	chr1:62656660-62780644	Flanking Active TSS Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv1013582	chr1:62723703-62910632	Flanking Active TSS Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	31 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:62753200-62760000	Weak transcription	Fetal Stomach	stomach
2	chr1:62753200-62761600	Weak transcription	Pancreas	Pancrea
3	chr1:62753200-62761600	Weak transcription	Right Atrium	heart
4	chr1:62754200-62760200	Weak transcription	Placenta	Placenta
5	chr1:62754400-62773400	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr1:62754800-62765200	Weak transcription	Fetal Heart	heart
7	chr1:62755000-62759800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr1:62755200-62759800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
9	chr1:62755600-62761000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
10	chr1:62756200-62765000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr1:62756400-62764800	Weak transcription	HepG2	liver
12	chr1:62757800-62760000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr1:62758400-62760000	Weak transcription	H1 Cell Line	embryonic stem cell

Quick Search: