Variant report

Variant rs370885520
Chromosome Location chr12:31220499-31220500
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:6 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:31189800-31225400 Weak transcription Fetal Stomach stomach
2 chr12:31210800-31225200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
3 chr12:31219600-31225600 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
4 chr12:31220400-31221000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr12:31220400-31221200 Enhancers HMEC breast
6 chr12:31220400-31221200 Enhancers NHEK skin

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