Variant report

Variant	rs16986152
Chromosome Location	chrX:110005836-110005837
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]
rs16986117	1.00[YRI][hapmap]
rs16986125	1.00[YRI][hapmap]
rs16986129	1.00[YRI][hapmap]
rs16986138	1.00[YRI][hapmap]
rs16986139	1.00[YRI][hapmap]
rs16986149	1.00[YRI][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	nsv817233	chrX:109693720-110244649	Weak transcription Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:109942600-110008200	Weak transcription	Primary hematopoietic stem cells	blood
2	chrX:109991800-110011600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chrX:110000800-110013200	Weak transcription	Fetal Brain Female	brain
4	chrX:110001800-110007600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chrX:110003200-110006800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chrX:110003400-110007600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chrX:110005600-110008800	Weak transcription	Rectal Smooth Muscle	rectum
8	chrX:110005800-110006000	ZNF genes & repeats	Adipose Nuclei	Adipose

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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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