Variant report

Variant	rs2031572
Chromosome Location	chr10:23433536-23433537
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:23432800-23433600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr10:23433000-23437200	Weak transcription	Pancreas	Pancrea

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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