| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:105489811-105489921 | Rare:17 | ||||
| chr14:105490622-105490781 | Rare:38 | ||||
| chr14:105490783-105491408 | Common:1; Rare:186 | ||||
| chr14:105491646-105491738 | Common:1; Rare:44 | ||||
| chr14:105528494-105528570 | Rare:17 | ||||
| chr15:22786106-22786401 | Common:3; Rare:78 | ||||
| chr15:22786410-22786735 | Common:1; Rare:118; Clinvar:2; Clinvar (benign):2 | ||||
| chr15:22787005-22787146 | Common:1; Rare:36 | ||||
| chr15:22787254-22787357 | Common:2; Rare:31 | ||||
| chr15:22838139-22838187 | Rare:9 | ||||
| chr15:22838189-22838268 | Rare:14 | ||||
| chr15:22838370-22838825 | Common:3; Rare:155 | ||||
| chr15:22838944-22839000 | Rare:16 | ||||
| chr15:22980285-22980559 | Common:1; Rare:99 | ||||
| chr15:22980659-22980786 | Common:4; Rare:47 |