| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:89243382-89243548 | Common:1; Rare:33 | ||||
| chr15:89243671-89244454 | Common:7; Rare:207; Clinvar:3 | ||||
| chr15:89334328-89334642 | Common:3; Rare:104 | ||||
| chr15:89334693-89335126 | Common:4; Rare:186; Clinvar:1; Clinvar (benign):1 | ||||
| chr15:89575107-89575564 | Common:5; Rare:138 | ||||
| chr15:89575885-89575985 | Rare:30 | ||||
| chr15:89576081-89576146 | Rare:20 | ||||
| chr15:89654887-89655056 | Common:1; Rare:33 | ||||
| chr15:89655361-89655608 | Common:1; Rare:84; Clinvar (benign):2 | ||||
| chr15:89690464-89690880 | Common:4; Rare:114 | ||||
| chr15:89750769-89751230 | Common:12; Rare:197 | ||||
| chr15:89776536-89776643 | Common:1; Rare:56; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):4 | ||||
| chr15:89814362-89814457 | Common:2; Rare:26 | ||||
| chr15:89814790-89814983 | Common:2; Rare:40 | ||||
| chr15:89815080-89815225 | Rare:23 |