Variant report
Variant | rs57018855 |
---|---|
Chromosome Location | chr11:59668485-59668486 |
allele | C/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr11:59660000-59668800 | Weak transcription | iPS-15b Cell Line | embryonic stem cell |
2 | chr11:59666200-59669800 | Weak transcription | Spleen | Spleen |
3 | chr11:59666400-59668800 | Weak transcription | K562 | blood |
4 | chr11:59667000-59669400 | Enhancers | Fetal Brain Female | brain |
5 | chr11:59667400-59669000 | Weak transcription | Fetal Brain Male | brain |
6 | chr11:59667600-59669000 | Enhancers | Foreskin Melanocyte Primary Cells skin03 | Skin |
7 | chr11:59668000-59669000 | Enhancers | HUVEC | blood vessel |
8 | chr11:59668200-59669000 | Enhancers | NH-A | brain |
9 | chr11:59668200-59669400 | Enhancers | NHEK | skin |
10 | chr11:59668400-59669200 | Enhancers | hESC Derived CD56+ Mesoderm Cultured Cells | ES cell derived |
11 | chr11:59668400-59669400 | Enhancers | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
12 | chr11:59668400-59669400 | Enhancers | Foreskin Keratinocyte Primary Cells skin03 | Skin |
13 | chr11:59668400-59669600 | Enhancers | Hela-S3 | cervix |