| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:103529090-103529223 | Common:1; Rare:41 | ||||
| chr14:103562282-103562394 | Rare:40 | ||||
| chr14:103562620-103563234 | Common:11; Rare:253; Clinvar:1; Clinvar (benign):9 | ||||
| chr14:103715437-103715851 | Common:1; Rare:140 | ||||
| chr14:104970469-104970815 | Common:4; Rare:66 | ||||
| chr14:105419751-105420032 | Rare:90 | ||||
| chr15:22838356-22838737 | Common:3; Rare:135 | ||||
| chr15:30903747-30903946 | Common:1; Rare:52 | ||||
| chr15:34101821-34102083 | Common:1; Rare:59 | ||||
| chr15:34988236-34988364 | Rare:55 | ||||
| chr15:35546137-35546256 | Common:1; Rare:42 | ||||
| chr15:37100500-37100809 | Common:1; Rare:101 | ||||
| chr15:39580813-39581147 | Common:2; Rare:95 | ||||
| chr15:39782820-39782899 | Rare:23 | ||||
| chr15:39933956-39934226 | Common:4; Rare:98 |