Variant report
Variant | rs58108137 |
---|---|
Chromosome Location | chr13:98049501-98049502 |
allele | A/G |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr13:97995400-98050200 | Weak transcription | Small Intestine | intestine |
2 | chr13:98028000-98056400 | Weak transcription | Psoas Muscle | Psoas |
3 | chr13:98039600-98054400 | Weak transcription | Primary T cells from cord blood | blood |
4 | chr13:98040000-98049800 | Weak transcription | Lung | lung |
5 | chr13:98041400-98050200 | Weak transcription | Fetal Stomach | stomach |
6 | chr13:98041800-98050800 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |
7 | chr13:98042000-98052800 | Weak transcription | Fetal Muscle Leg | muscle |
8 | chr13:98044600-98059400 | Weak transcription | Left Ventricle | heart |
9 | chr13:98045400-98059400 | Weak transcription | Breast Myoepithelial Primary Cells | Breast |
10 | chr13:98048200-98050200 | Weak transcription | Skeletal Muscle Female | skeletal muscle |
11 | chr13:98048400-98052200 | Weak transcription | NHLF | lung |
12 | chr13:98049000-98050200 | Enhancers | Fetal Lung | lung |
13 | chr13:98049200-98049800 | Enhancers | IMR90 fetal lung fibroblasts Cell Line | lung |
14 | chr13:98049200-98049800 | Enhancers | Colon Smooth Muscle | Colon |
15 | chr13:98049400-98049600 | Enhancers | Rectal Smooth Muscle | rectum |
16 | chr13:98049400-98050000 | Enhancers | Ganglion Eminence derived primary cultured neurospheres | brain |
17 | chr13:98049400-98050000 | Active TSS | Stomach Smooth Muscle | stomach |