Variant report

Variant	rs1360738
Chromosome Location	chr6:143310827-143310828
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs199249	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs199251	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs199252	0.82[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs199253	0.91[ASN][1000 genomes]
rs57083985	0.96[EUR][1000 genomes]
rs6570540	0.99[ASN][1000 genomes]
rs6570541	0.99[ASN][1000 genomes]
rs6570542	0.99[ASN][1000 genomes]
rs6570543	0.99[ASN][1000 genomes]
rs6570544	0.99[ASN][1000 genomes]
rs6901140	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7742621	0.99[ASN][1000 genomes]
rs7767231	0.98[ASN][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	nsv538459	chr6:143165802-143360098	Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Bivalent Enhancer Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	17 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	chr6:143309600-143312400	Weak transcription	Psoas Muscle	Psoas

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

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