Variant report

Variant	rs443810
Chromosome Location	chrX:91487513-91487514
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs118217	1.00[CHB][hapmap];1.00[YRI][hapmap]
rs118218	1.00[CHB][hapmap];1.00[YRI][hapmap]
rs2025088	1.00[CHB][hapmap]
rs2025090	1.00[CHB][hapmap]
rs2025093	0.85[YRI][hapmap]
rs373438	1.00[CHB][hapmap]
rs382841	1.00[CHB][hapmap];1.00[YRI][hapmap]
rs393785	1.00[CHB][hapmap];1.00[YRI][hapmap]
rs410882	1.00[CHB][hapmap];1.00[YRI][hapmap]
rs4141535	1.00[CHB][hapmap];1.00[YRI][hapmap]
rs4279764	1.00[CHB][hapmap];1.00[YRI][hapmap]
rs4281262	1.00[CHB][hapmap];1.00[YRI][hapmap]
rs435669	1.00[CHB][hapmap];1.00[YRI][hapmap]
rs4893173	1.00[CHB][hapmap]
rs4893309	0.89[YRI][hapmap]
rs5941044	1.00[CHB][hapmap]
rs5941045	1.00[CHB][hapmap]
rs5942137	1.00[CHB][hapmap]
rs5942141	1.00[CHB][hapmap]
rs5942153	1.00[CHB][hapmap];1.00[YRI][hapmap]
rs5942183	1.00[CHB][hapmap];1.00[YRI][hapmap]
rs5942186	1.00[CHB][hapmap];1.00[YRI][hapmap]
rs5942187	0.89[YRI][hapmap]
rs5984161	0.89[YRI][hapmap]
rs5984905	1.00[CHB][hapmap];0.94[YRI][hapmap]
rs5984909	0.89[YRI][hapmap]
rs5984912	1.00[CHB][hapmap]
rs6418101	1.00[CHB][hapmap];0.94[YRI][hapmap]
rs6522496	0.89[YRI][hapmap]
rs6652624	1.00[CHB][hapmap]
rs6652630	1.00[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv432350	chrX:91158935-91590765	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	esv3435339	chrX:91427773-91539017	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv532885	chrX:91428554-92377178	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv533436	chrX:91434301-91519622	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:91485800-91487600	Enhancers	ES-I3 Cell Line	embryonic stem cell
2	chrX:91487200-91492000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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