Variant report

Variant	rs10225438
Chromosome Location	chr7:116267129-116267130
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Variant related genes	Relation type
ENSG00000135269	Chromatin interaction
ENSG00000001626	Chromatin interaction
ENSG00000077063	Chromatin interaction
ENSG00000198898	Chromatin interaction

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:116267000-116267600	Active TSS	K562	blood

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

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