| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:23953576-23953726 | Common:4; Rare:59 | ||||
| chr14:23953730-23953835 | Common:4; Rare:36 | ||||
| chr14:23953977-23954399 | Common:3; Rare:120 | ||||
| chr14:23969819-23969966 | Common:7; Rare:62 | ||||
| chr14:23988689-23988727 | Common:3; Rare:13 | ||||
| chr14:23988729-23989007 | Common:10; Rare:123 | ||||
| chr14:24051834-24052020 | Common:2; Rare:53 | ||||
| chr14:24081618-24081715 | Common:1; Rare:26 | ||||
| chr14:24093859-24094430 | Common:5; Rare:146; Clinvar (benign):1 | ||||
| chr14:24094484-24094707 | Rare:55 | ||||
| chr14:24095560-24095749 | Common:1; Rare:39 | ||||
| chr14:24114732-24115364 | Common:3; Rare:173 | ||||
| chr14:24135897-24136263 | Common:1; Rare:112 | ||||
| chr14:24136445-24136571 | Rare:27 | ||||
| chr14:24140487-24140937 | Common:1; Rare:101 |