Variant report

Variant	rs5916866
Chromosome Location	chrX:104352535-104352536
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11092531	0.93[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs12854780	0.88[CEU][hapmap]
rs1590197	1.00[YRI][hapmap]
rs1894447	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2009995	0.93[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap]
rs2392686	0.87[CEU][hapmap]
rs2858229	1.00[YRI][hapmap]
rs4826890	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap]
rs4826914	0.93[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs4826915	0.93[CEU][hapmap];0.84[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs4826916	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs5916723	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs5916724	1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap]
rs5916729	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs5916730	1.00[YRI][hapmap]
rs5916731	1.00[YRI][hapmap]
rs5916865	0.81[JPT][hapmap]
rs5916870	1.00[CEU][hapmap];0.84[CHB][hapmap];1.00[JPT][hapmap]
rs5916873	0.93[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs5916874	0.93[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap]
rs5916875	1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap]
rs5916876	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap]
rs5962466	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs5962469	0.93[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap]
rs6616564	0.80[JPT][hapmap];1.00[YRI][hapmap]
rs6616565	1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap]
rs6616567	0.93[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs6616570	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap]
rs6616576	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs6621920	1.00[YRI][hapmap]
rs6621926	0.81[JPT][hapmap]
rs6621930	1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap]
rs6621931	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6621938	0.93[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs6621941	1.00[CEU][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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