Variant report
Variant | rs73709640 |
---|---|
Chromosome Location | chr7:98916196-98916197 |
allele | A/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr7:98908000-98917800 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
2 | chr7:98908200-98922600 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |
3 | chr7:98908400-98921800 | Weak transcription | Foreskin Fibroblast Primary Cells skin01 | Skin |
4 | chr7:98908400-98923000 | Weak transcription | Aorta | Aorta |
5 | chr7:98910200-98921800 | Weak transcription | Right Ventricle | heart |
6 | chr7:98910600-98922600 | Weak transcription | Brain Inferior Temporal Lobe | brain |
7 | chr7:98911000-98922400 | Weak transcription | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
8 | chr7:98911000-98922400 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
9 | chr7:98911000-98922600 | Weak transcription | NHLF | lung |
10 | chr7:98911200-98922600 | Weak transcription | Brain Substantia Nigra | brain |
11 | chr7:98911400-98922600 | Weak transcription | A549 | lung |
12 | chr7:98912200-98921800 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
13 | chr7:98912400-98919000 | Weak transcription | Stomach Mucosa | stomach |
14 | chr7:98912600-98921800 | Weak transcription | Foreskin Fibroblast Primary Cells skin02 | Skin |
15 | chr7:98912600-98922200 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
16 | chr7:98914600-98918000 | Weak transcription | ES-I3 Cell Line | embryonic stem cell |
17 | chr7:98915000-98922600 | Weak transcription | H9 Cell Line | embryonic stem cell |
18 | chr7:98915400-98918200 | Weak transcription | Fetal Intestine Small | intestine |