Variant report

Variant	rs373922658
Chromosome Location	chr12:75009015-75009016
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 0)

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	esv3325789	chr12:75006185-75011483	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
2	esv3359036	chr12:75008085-75011183	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
3	esv2442822	chr12:75008212-75010939	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a
4	esv3322458	chr12:75008485-75010933	Weak transcription Enhancers	n/a	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:75008800-75012600	Weak transcription	Hela-S3	cervix

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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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