Variant report

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs10227883	1.00[ASN][1000 genomes]
rs10228286	1.00[ASN][1000 genomes]
rs10249504	1.00[ASN][1000 genomes]
rs10249601	1.00[ASN][1000 genomes]
rs10257029	1.00[ASN][1000 genomes]
rs10257782	1.00[ASN][1000 genomes]
rs10278693	1.00[ASN][1000 genomes]
rs10282173	1.00[ASN][1000 genomes]
rs13437692	1.00[ASN][1000 genomes]
rs17171416	1.00[ASN][1000 genomes]
rs17171420	1.00[ASN][1000 genomes]
rs17171421	1.00[ASN][1000 genomes]
rs17346292	1.00[ASN][1000 genomes]
rs17415102	0.87[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17415529	1.00[ASN][1000 genomes]
rs17500381	0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1864887	1.00[ASN][1000 genomes]
rs1864888	1.00[ASN][1000 genomes]
rs28393755	1.00[ASN][1000 genomes]
rs28479083	1.00[ASN][1000 genomes]
rs28504175	1.00[ASN][1000 genomes]
rs28510981	1.00[ASN][1000 genomes]
rs28549342	1.00[ASN][1000 genomes]
rs28578669	1.00[ASN][1000 genomes]
rs28754843	1.00[ASN][1000 genomes]
rs4723775	0.87[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4723776	0.85[AMR][1000 genomes]
rs73692926	1.00[ASN][1000 genomes]
rs73692927	1.00[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	nsv932229	chr7:38248340-38727527	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:38671400-38677600	Weak transcription	Right Atrium	heart
2	chr7:38671800-38673600	Weak transcription	Fetal Brain Female	brain

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