Variant report

Variant	rs12014093
Chromosome Location	chrX:77631366-77631367
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 3 )
Associated
traits (count: 0)

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	nsv529299	chrX:77040316-77947157	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
2	nsv532880	chrX:77085352-77769755	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
3	nsv492122	chrX:77450503-77664330	Enhancers ZNF genes & repeats Active TSS Strong transcription Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:77630400-77631600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chrX:77630600-77632800	Enhancers	Dnd41	blood
3	chrX:77630800-77631400	Enhancers	Primary T helper naive cells from peripheral blood	blood
4	chrX:77630800-77631800	Enhancers	NHEK	skin
5	chrX:77630800-77632800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chrX:77631000-77631400	Enhancers	Placenta	Placenta
7	chrX:77631000-77631600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
8	chrX:77631000-77631600	Enhancers	Primary T helper cells PMA-I stimulated	--
9	chrX:77631000-77631600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chrX:77631200-77631600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--

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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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