| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:89912903-89913072 | Common:2; Rare:46 | ||||
| chr15:90001333-90001477 | Rare:36 | ||||
| chr15:90184652-90184982 | Common:2; Rare:76 | ||||
| chr15:90190521-90190713 | Common:2; Rare:28 | ||||
| chr15:90201071-90201577 | Common:4; Rare:178 | ||||
| chr15:90233864-90234265 | Common:6; Rare:114 | ||||
| chr15:90265634-90265727 | Rare:41 | ||||
| chr15:90352116-90352324 | Common:4; Rare:54 | ||||
| chr15:90387962-90388393 | Common:5; Rare:173 | ||||
| chr15:90717095-90717428 | Common:1; Rare:84; Clinvar:3 | ||||
| chr15:90884369-90884509 | Common:3; Rare:35 | ||||
| chr15:90954729-90954940 | Common:3; Rare:59 | ||||
| chr15:90955262-90955395 | Rare:33 | ||||
| chr15:90994410-90994881 | Common:1; Rare:173 | ||||
| chr15:91022446-91022723 | Common:1; Rare:72; Clinvar:3; Clinvar (benign):1 |