Variant report

Variant	rs6036668
Chromosome Location	chr20:24133456-24133457
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs127801	0.85[EUR][1000 genomes]
rs1884520	0.87[ASN][1000 genomes]
rs1884521	0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2013711	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2208013	0.92[ASN][1000 genomes]
rs224153	0.86[EUR][1000 genomes]
rs2749424	0.82[EUR][1000 genomes]
rs2890401	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6036665	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6036670	0.85[ASN][1000 genomes]
rs6049429	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6049432	0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6049434	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6049435	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6049439	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6049443	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6049446	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6049453	0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6049454	0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6049455	0.92[ASN][1000 genomes]
rs6049458	0.92[ASN][1000 genomes]
rs6049460	0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6049461	0.90[ASN][1000 genomes]
rs6049467	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6083394	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6083397	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6114503	0.95[ASN][1000 genomes]
rs6114507	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6114508	0.90[ASN][1000 genomes]
rs6114509	0.90[ASN][1000 genomes]
rs761868	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs761869	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs761870	0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs910780	0.90[ASN][1000 genomes]
rs910781	0.87[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	nsv9793	chr20:23939613-24734850	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	esv3328348	chr20:24095746-24285830	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:24131400-24134000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr20:24131600-24134600	Enhancers	Fetal Muscle Leg	muscle
3	chr20:24133200-24133800	Active TSS	Fetal Muscle Trunk	muscle
4	chr20:24133400-24134200	Enhancers	iPS-18 Cell Line	embryonic stem cell

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