Variant report

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10106386	0.92[EUR][1000 genomes]
rs1025856	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10808406	0.87[EUR][1000 genomes]
rs11776679	0.95[AFR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12541049	0.81[ASN][1000 genomes]
rs12542643	0.92[EUR][1000 genomes]
rs12545946	0.95[ASN][1000 genomes]
rs12546300	0.84[EUR][1000 genomes]
rs12550547	0.87[ASN][1000 genomes]
rs1372621	0.94[ASN][1000 genomes]
rs1578995	0.92[EUR][1000 genomes]
rs1992471	0.92[EUR][1000 genomes]
rs2028552	0.89[ASN][1000 genomes]
rs28565020	0.99[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs3779776	0.94[ASN][1000 genomes]
rs6469013	0.90[ASN][1000 genomes]
rs6992301	0.99[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7003445	0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs73305060	0.94[ASN][1000 genomes]
rs73305067	0.95[ASN][1000 genomes]
rs73305069	0.94[ASN][1000 genomes]
rs753534	0.94[ASN][1000 genomes]
rs753535	0.94[ASN][1000 genomes]
rs753536	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7816793	0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7823563	0.85[AFR][1000 genomes];0.97[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7836133	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.92[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	nsv1021369	chr8:106493317-107243322	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
2	nsv831418	chr8:106648456-106833333	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:106647400-106735200	Weak transcription	K562	blood
2	chr8:106721000-106735400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr8:106729200-106736400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr8:106729200-106742600	Weak transcription	Right Ventricle	heart
5	chr8:106734200-106738000	Weak transcription	Ovary	ovary
6	chr8:106734200-106743200	Weak transcription	Aorta	Aorta

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