Variant report

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs16869976	0.87[ASN][1000 genomes]
rs16869978	0.87[ASN][1000 genomes]
rs2513873	0.87[ASN][1000 genomes]
rs2513874	0.85[ASN][1000 genomes]
rs2646307	0.85[ASN][1000 genomes]
rs28372883	0.87[ASN][1000 genomes]
rs3824225	0.87[ASN][1000 genomes]
rs3824228	0.87[ASN][1000 genomes]
rs473142	0.82[ASN][1000 genomes]
rs473152	0.82[ASN][1000 genomes]
rs486506	0.91[ASN][1000 genomes]
rs488420	0.91[ASN][1000 genomes]
rs492701	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs556059	0.81[AMR][1000 genomes]
rs613121	0.88[ASN][1000 genomes]
rs615348	0.88[ASN][1000 genomes]
rs62525309	0.87[ASN][1000 genomes]
rs628793	0.91[ASN][1000 genomes]
rs630236	0.91[ASN][1000 genomes]
rs631019	0.91[ASN][1000 genomes]
rs642994	0.90[ASN][1000 genomes]
rs644305	0.91[ASN][1000 genomes]
rs677398	0.87[ASN][1000 genomes]
rs677415	0.87[ASN][1000 genomes]
rs681859	0.86[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv33118	chr8:103358567-104068172	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	145 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:104013400-104017400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell

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