Variant report
Variant | rs57982245 |
---|---|
Chromosome Location | chr16:70639102-70639103 |
allele | C/G |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr16:70626200-70644200 | Weak transcription | Right Atrium | heart |
2 | chr16:70626400-70642200 | Weak transcription | Esophagus | oesophagus |
3 | chr16:70626400-70644200 | Weak transcription | Lung | lung |
4 | chr16:70626400-70644200 | Weak transcription | Stomach Smooth Muscle | stomach |
5 | chr16:70629600-70644000 | Weak transcription | Fetal Muscle Leg | muscle |
6 | chr16:70633200-70640600 | Weak transcription | Fetal Stomach | stomach |
7 | chr16:70636000-70640600 | Strong transcription | Fetal Intestine Small | intestine |
8 | chr16:70636400-70644200 | Weak transcription | Duodenum Mucosa | Duodenum |
9 | chr16:70637400-70639200 | Enhancers | Breast Myoepithelial Primary Cells | Breast |
10 | chr16:70637800-70639200 | Enhancers | Brain Hippocampus Middle | brain |
11 | chr16:70637800-70639400 | Enhancers | Brain Substantia Nigra | brain |
12 | chr16:70638600-70639200 | Bivalent Enhancer | Foreskin Fibroblast Primary Cells skin01 | Skin |
13 | chr16:70638600-70639200 | Enhancers | Fetal Muscle Trunk | muscle |
14 | chr16:70638600-70639400 | Bivalent Enhancer | Foreskin Fibroblast Primary Cells skin02 | Skin |
15 | chr16:70638800-70639200 | ZNF genes & repeats | iPS DF 19.11 Cell Line | embryonic stem cell |
16 | chr16:70638800-70639200 | Enhancers | Skeletal Muscle Male | skeletal muscle |
17 | chr16:70639000-70639200 | Enhancers | Spleen | Spleen |
18 | chr16:70639000-70639800 | Enhancers | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |
19 | chr16:70639000-70642000 | Weak transcription | Fetal Intestine Large | intestine |