| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:104826558-104826768 | Common:5; Rare:47 | ||||
| chr15:22494640-22494916 | Common:1; Rare:35 | ||||
| chr15:22664577-22665007 | Common:7; Rare:131 | ||||
| chr15:22715440-22715795 | Common:3; Rare:88 | ||||
| chr15:23303469-23303765 | Rare:19 | ||||
| chr15:24859006-24859188 | Common:1; Rare:34 | ||||
| chr15:25056561-25056860 | Common:3; Rare:94 | ||||
| chr15:25088052-25088588 | Common:4; Rare:155 | ||||
| chr15:25093892-25094037 | Common:3; Rare:36 | ||||
| chr15:26082309-26082472 | Common:4; Rare:78 | ||||
| chr15:28589201-28589534 | Common:1; Rare:10 | ||||
| chr15:29730329-29730611 | Common:1; Rare:51 | ||||
| chr15:29925006-29925202 | Rare:24 | ||||
| chr15:32536450-32536773 | Common:2; Rare:38 | ||||
| chr15:34791051-34791420 | Common:11; Rare:86; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):2 |