Variant report

Variant	rs7881764
Chromosome Location	chrX:104407005-104407006
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1155915	0.81[ASW][hapmap];0.82[YRI][hapmap]
rs16984623	1.00[ASW][hapmap];1.00[MEX][hapmap];1.00[YRI][hapmap]
rs2392685	1.00[MEX][hapmap]
rs5963017	1.00[MEX][hapmap]
rs6621922	1.00[MEX][hapmap]
rs7052838	1.00[ASW][hapmap];1.00[MEX][hapmap];1.00[YRI][hapmap]
rs7055384	0.81[ASW][hapmap]
rs7066121	1.00[ASW][hapmap];1.00[MEX][hapmap];1.00[YRI][hapmap]
rs7883092	1.00[ASW][hapmap];1.00[MEX][hapmap];1.00[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2758580	chrX:104303006-104415037	Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases
2	esv2758881	chrX:104303006-104415037	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
3	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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