| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:43330539-43330694 | Rare:58 | ||||
| chr15:43371039-43371233 | Common:1; Rare:39 | ||||
| chr15:43510833-43510954 | Rare:35 | ||||
| chr15:43648839-43649021 | Common:2; Rare:73 | ||||
| chr15:43746275-43746575 | Common:1; Rare:128 | ||||
| chr15:43776964-43777393 | Rare:109 | ||||
| chr15:43824632-43824860 | Common:2; Rare:61 | ||||
| chr15:44288374-44288991 | Common:39; Rare:290 | ||||
| chr15:44536663-44537203 | Common:1; Rare:164 | ||||
| chr15:44663556-44663717 | Rare:96; Clinvar:11; Clinvar (benign):6 | ||||
| chr15:44711341-44711611 | Rare:83; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:44711849-44711990 | Rare:27 | ||||
| chr15:45378482-45378718 | Common:3; Rare:63; Clinvar:1; Clinvar (benign):3 | ||||
| chr15:45522557-45522682 | Rare:30 | ||||
| chr15:45587115-45587273 | Rare:28 |