Variant report
Variant | rs6745453 |
---|---|
Chromosome Location | chr2:38623850-38623851 |
allele | A/G/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:38605200-38624400 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
2 | chr2:38612200-38633200 | Weak transcription | Stomach Smooth Muscle | stomach |
3 | chr2:38620200-38625800 | Enhancers | Foreskin Keratinocyte Primary Cells skin02 | Skin |
4 | chr2:38620600-38624200 | Enhancers | HMEC | breast |
5 | chr2:38621200-38624600 | Enhancers | Foreskin Melanocyte Primary Cells skin03 | Skin |
6 | chr2:38622200-38626600 | Enhancers | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
7 | chr2:38622600-38624000 | Enhancers | Fetal Adrenal Gland | Adrenal Gland |
8 | chr2:38622800-38624000 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
9 | chr2:38623000-38624800 | Weak transcription | Breast Myoepithelial Primary Cells | Breast |
10 | chr2:38623800-38625200 | Weak transcription | NHEK | skin |