| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:197749656-197749938 | Common:1; Rare:86 | ||||
| chr3:197949893-197950264 | Common:4; Rare:114; Clinvar (benign):2 | ||||
| chr4:474127-474351 | Common:2; Rare:72 | ||||
| chr4:499128-499257 | Common:3; Rare:45 | ||||
| chr4:674252-674566 | Common:2; Rare:146 | ||||
| chr4:932259-932492 | Common:2; Rare:90 | ||||
| chr4:1289670-1289906 | Common:1; Rare:75 | ||||
| chr4:2468939-2469159 | Common:1; Rare:69 | ||||
| chr4:2812066-2812295 | Rare:35 | ||||
| chr4:2843658-2843979 | Common:3; Rare:116 | ||||
| chr4:2934813-2934910 | Common:1; Rare:50 | ||||
| chr4:2963338-2963603 | Common:2; Rare:92 | ||||
| chr4:4248209-4248254 | Common:1; Rare:16 | ||||
| chr4:4290110-4290277 | Common:3; Rare:69 | ||||
| chr4:4541978-4542143 | Common:1; Rare:65 |