Variant report

Variant rs373478272
Chromosome Location chr14:44840607-44840608
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:5 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:44838400-44842600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
2 chr14:44839400-44841200 Weak transcription Fetal Intestine Large intestine
3 chr14:44839600-44841400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr14:44839800-44841200 Weak transcription HMEC breast
5 chr14:44840200-44841200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin

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