Variant report

Variant	rs12131464
Chromosome Location	chr1:168899457-168899458
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs10489363	0.94[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10489366	0.94[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12133503	0.94[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12134708	0.91[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12562255	0.94[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs16861737	0.94[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2419395	0.94[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs41271661	0.82[AMR][1000 genomes]
rs7518480	0.94[AMR][1000 genomes];0.84[EUR][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	nsv869415	chr1:168467284-169153863	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	44 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:168896400-168901600	Weak transcription	Fetal Heart	heart

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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