Variant report

Variant	rs71537498
Chromosome Location	chrX:93131983-93131984
allele	AC/GA
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs484267	0.82[AFR][1000 genomes]

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	nsv916355	chrX:92984966-93234497	Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:93130000-93132200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
2	chrX:93130200-93132400	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
3	chrX:93130800-93133200	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
4	chrX:93131000-93132200	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
5	chrX:93131400-93134600	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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