Variant report
Variant | rs78678612 |
---|---|
Chromosome Location | chr5:150942392-150942393 |
allele | G/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr5:150908200-150948000 | Strong transcription | HMEC | breast |
2 | chr5:150908400-150944000 | Strong transcription | NHEK | skin |
3 | chr5:150909200-150942400 | Strong transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
4 | chr5:150911600-150942800 | Strong transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
5 | chr5:150918200-150945400 | Strong transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
6 | chr5:150931000-150942800 | Weak transcription | Brain Angular Gyrus | brain |
7 | chr5:150934200-150949600 | Weak transcription | Skeletal Muscle Male | skeletal muscle |
8 | chr5:150937000-150948600 | Weak transcription | Right Atrium | heart |
9 | chr5:150937600-150948600 | Weak transcription | Adipose Nuclei | Adipose |
10 | chr5:150940800-150942600 | Enhancers | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
11 | chr5:150940800-150943200 | Genic enhancers | Breast Myoepithelial Primary Cells | Breast |
12 | chr5:150941400-150942600 | Enhancers | iPS-20b Cell Line | embryonic stem cell |
13 | chr5:150942200-150942800 | Strong transcription | Esophagus | oesophagus |