Variant report

Variant	rs1122799
Chromosome Location	chrX:55005850-55005851
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs11541054	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs17002406	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap]
rs2885192	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs7058892	1.00[JPT][hapmap]
rs7059574	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs7881427	1.00[JPT][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	nsv6912	chrX:54980516-55025317	Flanking Active TSS Active TSS Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:55004600-55023800	Weak transcription	Psoas Muscle	Psoas
2	chrX:55005400-55008000	Weak transcription	Skeletal Muscle Male	skeletal muscle
3	chrX:55005600-55006000	Weak transcription	Liver	Liver

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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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