Variant report

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10215129	1.00[ASN][1000 genomes]
rs10216139	1.00[ASN][1000 genomes]
rs10235715	1.00[ASN][1000 genomes]
rs10237943	0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10244209	1.00[ASN][1000 genomes]
rs10249076	1.00[ASN][1000 genomes]
rs10254377	0.82[EUR][1000 genomes]
rs10254450	1.00[ASN][1000 genomes]
rs10258085	0.83[EUR][1000 genomes]
rs10268557	1.00[ASN][1000 genomes]
rs10269811	1.00[ASN][1000 genomes]
rs10275579	1.00[ASN][1000 genomes]
rs10279562	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10488626	1.00[ASN][1000 genomes]
rs1425157	1.00[ASN][1000 genomes]
rs17168743	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28445653	1.00[ASN][1000 genomes]
rs28687373	1.00[ASN][1000 genomes]
rs56349320	1.00[ASN][1000 genomes]
rs7778136	1.00[ASN][1000 genomes]
rs7809833	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv518439	chr7:136134265-136452082	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv508484	chr7:136333249-136384790	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:136377400-136381600	Weak transcription	Fetal Heart	heart

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