| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:103529081-103529233 | Common:1; Rare:47 | ||||
| chr14:103562624-103563059 | Common:8; Rare:173; Clinvar (benign):5 | ||||
| chr14:104752859-104753220 | Common:3; Rare:123 | ||||
| chr14:104970476-104970781 | Common:4; Rare:60 | ||||
| chr14:105419733-105420032 | Rare:95 | ||||
| chr15:23686801-23687037 | Rare:92 | ||||
| chr15:25439035-25439209 | Common:1; Rare:63 | ||||
| chr15:30903793-30903943 | Rare:36 | ||||
| chr15:32615111-32615150 | Common:1; Rare:13 | ||||
| chr15:32615163-32615603 | Common:6; Rare:107 | ||||
| chr15:33310638-33311020 | Common:1; Rare:110 | ||||
| chr15:34101810-34102105 | Common:1; Rare:68 | ||||
| chr15:34318765-34318909 | Common:1; Rare:33 | ||||
| chr15:34588444-34588584 | Rare:38 | ||||
| chr15:35546137-35546269 | Common:1; Rare:47 |