Variant report

Variant	rs73715928
Chromosome Location	chr7:103597707-103597708
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:103596000-103599000	Strong transcription	HepG2	liver
2	chr7:103596600-103598200	Enhancers	Fetal Heart	heart
3	chr7:103597200-103599000	Strong transcription	K562	blood

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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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