Variant report

Variant	rs13440863
Chromosome Location	chrX:104659162-104659163
allele	C/T
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]
rs12392726	1.00[ASW][hapmap];0.90[MKK][hapmap]
rs16984759	1.00[ASW][hapmap]
rs16984763	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[YRI][hapmap]
rs5962281	0.93[LWK][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap]
rs5962285	1.00[ASW][hapmap];0.90[MKK][hapmap]
rs5962517	1.00[ASW][hapmap]
rs5962520	1.00[ASW][hapmap];0.90[MKK][hapmap]
rs5962521	1.00[ASW][hapmap]
rs6652922	0.92[LWK][hapmap];0.83[YRI][hapmap]

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	nsv432352	chrX:104346855-104831855	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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