| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30571890-30572051 | Common:1; Rare:24 | ||||
| chr16:30572300-30572650 | Rare:60 | ||||
| chr16:30585513-30586070 | Common:2; Rare:212 | ||||
| chr16:30609540-30609920 | Rare:180 | ||||
| chr16:30610234-30610570 | Common:2; Rare:165 | ||||
| chr16:30650555-30651010 | Rare:224 | ||||
| chr16:30651280-30651660 | Rare:168 | ||||
| chr16:30657931-30658502 | Common:2; Rare:223 | ||||
| chr16:30658589-30658864 | Common:1; Rare:83 | ||||
| chr16:30658887-30659149 | Rare:94 | ||||
| chr16:30697982-30698255 | Common:2; Rare:233 | ||||
| chr16:30698402-30698727 | Common:2; Rare:196 | ||||
| chr16:30698937-30699412 | Rare:246; Clinvar (benign):2 | ||||
| chr16:30748116-30748465 | Common:4; Rare:167; Clinvar:4; Clinvar (benign):2 | ||||
| chr16:30761308-30761787 | Common:3; Rare:314 |