Variant report

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs1158586	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1364407	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1364409	0.99[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1378645	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1378646	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1378647	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1455857	0.90[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1455858	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1469179	0.89[AFR][1000 genomes]
rs1824024	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2350783	0.85[AMR][1000 genomes]
rs6467695	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6467696	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6942627	0.81[AMR][1000 genomes]
rs6943950	0.81[AMR][1000 genomes]
rs6945230	0.81[ASN][1000 genomes]
rs6952264	0.81[AMR][1000 genomes]
rs6960707	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7782965	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs978437	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[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	nsv1029192	chr7:136433278-137147566	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv831147	chr7:136583444-136755741	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:136607800-136638000	Weak transcription	NHLF	lung
2	chr7:136610800-136623400	Weak transcription	Colon Smooth Muscle	Colon
3	chr7:136611000-136623200	Weak transcription	Left Ventricle	heart
4	chr7:136616600-136622600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr7:136617000-136620600	Weak transcription	Fetal Heart	heart

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