Variant report

Variant	rs7767298
Chromosome Location	chr6:82408186-82408187
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:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:82406600-82408400	Enhancers	Hela-S3	cervix
2	chr6:82407400-82408200	Weak transcription	Psoas Muscle	Psoas
3	chr6:82407400-82408600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr6:82407400-82410200	Weak transcription	Fetal Heart	heart
5	chr6:82407800-82410200	Weak transcription	HSMM	muscle
6	chr6:82407800-82411000	Weak transcription	Osteobl	bone

Quick Search:

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

what's new

Quick links