| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:113208620-113208751 | Rare:78 | ||||
| chr13:113490699-113491017 | Common:1; Rare:117 | ||||
| chr13:114234807-114235120 | Common:15; Rare:115 | ||||
| chr13:114281318-114281657 | Common:5; Rare:134 | ||||
| chr14:20343190-20343652 | Common:12; Rare:269 | ||||
| chr14:20413404-20413509 | Common:2; Rare:28 | ||||
| chr14:20455123-20455287 | Common:2; Rare:56 | ||||
| chr14:20684467-20684629 | Common:1; Rare:26; Clinvar (benign):1 | ||||
| chr14:20989685-20990011 | Common:7; Rare:73 | ||||
| chr14:21437222-21437437 | Common:4; Rare:91 | ||||
| chr14:21456051-21456359 | Common:3; Rare:79 | ||||
| chr14:21476849-21477267 | Common:2; Rare:138 | ||||
| chr14:21511300-21511429 | Rare:29 | ||||
| chr14:22589150-22589530 | Common:4; Rare:114 | ||||
| chr14:22766554-22766727 | Common:1; Rare:97 |