Variant report

Variant rs17114922
Chromosome Location chr14:44839028-44839029
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:6 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:44837400-44839200 Weak transcription Fetal Heart heart
2 chr14:44838200-44839400 Enhancers Fetal Intestine Large intestine
3 chr14:44838200-44839600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr14:44838400-44842600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
5 chr14:44838600-44839400 Enhancers NHEK skin
6 chr14:44838800-44839200 Enhancers HMEC breast

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