Variant report

Variant	rs12176238
Chromosome Location	chr6:82408565-82408566
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 1 )
Associated
traits (count: 0)

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	nsv1027683	chr6:82408186-82426855	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:82407400-82408600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr6:82407400-82410200	Weak transcription	Fetal Heart	heart
3	chr6:82407800-82410200	Weak transcription	HSMM	muscle
4	chr6:82407800-82411000	Weak transcription	Osteobl	bone
5	chr6:82408400-82409800	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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