| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:14932474-14932612 | Rare:12 | ||||
| chr16:14983021-14983153 | Common:1; Rare:11 | ||||
| chr16:14995239-14995299 | Rare:6 | ||||
| chr16:15007452-15007516 | Rare:8 | ||||
| chr16:15021945-15021995 | Rare:6 | ||||
| chr16:15026258-15026456 | Rare:20 | ||||
| chr16:15028335-15028428 | Rare:4 | ||||
| chr16:15127460-15127533 | Common:1; Rare:30 | ||||
| chr16:15142691-15142803 | Common:1; Rare:38 | ||||
| chr16:15704149-15704353 | Rare:54 | ||||
| chr16:15705932-15706061 | Common:3; Rare:24 | ||||
| chr16:15708779-15708845 | Rare:33; Clinvar:7; Clinvar (benign):3 | ||||
| chr16:15708871-15708949 | Rare:22 | ||||
| chr16:15715135-15715317 | Common:1; Rare:54; Clinvar:4; Clinvar (benign):8 | ||||
| chr16:15720121-15720565 | Common:1; Rare:128; Clinvar:12; Clinvar (benign):11; Clinvar (pathogenic):2 |