Variant report

Variant	rs12549932
Chromosome Location	chr8:49654515-49654516
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:49648600-49655400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr8:49648600-49661000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr8:49649800-49660200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr8:49651400-49656000	Weak transcription	Fetal Lung	lung
5	chr8:49653600-49654600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr8:49653600-49654800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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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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