| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:89756888-89757288 | Common:4; Rare:181 | ||||
| chr15:89782085-89782816 | Common:3; Rare:261 | ||||
| chr15:89785480-89785790 | Common:5; Rare:153 | ||||
| chr15:89828540-89828940 | Common:4; Rare:96 | ||||
| chr15:89858746-89859390 | Common:16; Rare:229 | ||||
| chr15:89957920-89958450 | Common:11; Rare:185 | ||||
| chr15:90034451-90034876 | Common:6; Rare:154 | ||||
| chr15:90034890-90035370 | Common:4; Rare:113 | ||||
| chr15:90035540-90036118 | Common:5; Rare:240 | ||||
| chr15:90046905-90047230 | Common:6; Rare:92 | ||||
| chr15:90047262-90047499 | Common:1; Rare:40 | ||||
| chr15:90088159-90088930 | Common:5; Rare:591; Clinvar:4; Clinvar (benign):9; Clinvar (pathogenic):8 | ||||
| chr15:90104734-90104900 | Common:4; Rare:35 | ||||
| chr15:90106440-90107130 | Rare:261 | ||||
| chr15:90149425-90149611 | Common:3; Rare:36 |