Variant report

Variant	rs146391433
Chromosome Location	chrX:75540196-75540197
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 1 )
Associated
traits (count: 0)

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	esv2830377	chrX:75525310-76337197	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:75539000-75540400	Enhancers	Primary T cells fromperipheralblood	blood
2	chrX:75539000-75540400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
3	chrX:75539000-75540600	Enhancers	Primary T helper cells PMA-I stimulated	--
4	chrX:75539000-75540600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
5	chrX:75539200-75540400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
6	chrX:75539200-75540600	Enhancers	Primary T helper cells fromperipheralblood	blood
7	chrX:75539400-75540400	Enhancers	Primary T killer memory cells from peripheral blood	blood

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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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