Variant report

Variant rs57990032
Chromosome Location chr14:68498924-68498925
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:68494800-68506200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
2 chr14:68495600-68500200 Weak transcription Pancreas Pancrea
3 chr14:68497400-68506200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr14:68498000-68499200 Weak transcription Fetal Kidney kidney
5 chr14:68498400-68499600 Weak transcription Primary hematopoietic stem cells blood
6 chr14:68498600-68500000 Enhancers Ovary ovary
7 chr14:68498800-68499800 Enhancers Fetal Intestine Small intestine
8 chr14:68498800-68500000 Enhancers Fetal Adrenal Gland Adrenal Gland
9 chr14:68498800-68503600 Enhancers Fetal Lung lung

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