| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:4493155-4493483 | Common:1; Rare:117; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:4978622-4978809 | Common:2; Rare:54 | ||||
| chr3:4979147-4979547 | Common:2; Rare:92 | ||||
| chr3:4980372-4980517 | Rare:38 | ||||
| chr3:5187304-5187663 | Common:5; Rare:139 | ||||
| chr3:8501505-8501604 | Rare:24 | ||||
| chr3:8501606-8501969 | Common:3; Rare:138 | ||||
| chr3:9362971-9363117 | Common:1; Rare:54 | ||||
| chr3:9397434-9397891 | Common:1; Rare:145 | ||||
| chr3:9749773-9750337 | Common:2; Rare:182 | ||||
| chr3:9769845-9770057 | Common:1; Rare:53 | ||||
| chr3:9792382-9792596 | Rare:59 | ||||
| chr3:9792705-9793123 | Common:3; Rare:148 | ||||
| chr3:9810207-9810394 | Common:1; Rare:72 | ||||
| chr3:9843952-9844028 | Common:1; Rare:45 |