Variant report
Variant | rs141825368 |
---|---|
Chromosome Location | chr1:212079894-212079895 |
allele | C/G |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:212076200-212080000 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
2 | chr1:212076200-212080800 | Weak transcription | Esophagus | oesophagus |
3 | chr1:212076200-212083600 | Weak transcription | Pancreas | Pancrea |
4 | chr1:212077200-212082600 | Weak transcription | Colonic Mucosa | Colon |
5 | chr1:212077400-212082400 | Weak transcription | Adipose Nuclei | Adipose |
6 | chr1:212078000-212082400 | Weak transcription | Duodenum Mucosa | Duodenum |
7 | chr1:212078000-212082400 | Weak transcription | HepG2 | liver |
8 | chr1:212078400-212081800 | Weak transcription | Liver | Liver |
9 | chr1:212078800-212080400 | Weak transcription | Fetal Intestine Large | intestine |
10 | chr1:212078800-212080800 | Weak transcription | Fetal Intestine Small | intestine |
11 | chr1:212079600-212087400 | Weak transcription | iPS DF 6.9 Cell Line | embryonic stem cell |
12 | chr1:212079800-212080000 | Enhancers | Primary monocytes fromperipheralblood | blood |