Variant report
Variant | rs13032601 |
---|---|
Chromosome Location | chr2:145955175-145955176 |
allele | A/G |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:145949200-145956800 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |
2 | chr2:145952400-145956400 | Weak transcription | Fetal Kidney | kidney |
3 | chr2:145952600-145956400 | Weak transcription | Stomach Mucosa | stomach |
4 | chr2:145952600-145957800 | Weak transcription | H9 Cell Line | embryonic stem cell |
5 | chr2:145953600-145956600 | Weak transcription | ES-I3 Cell Line | embryonic stem cell |
6 | chr2:145954400-145956800 | Weak transcription | Left Ventricle | heart |
7 | chr2:145955000-145956400 | Weak transcription | Fetal Heart | heart |
8 | chr2:145955000-145956600 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |