| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:119702399-119702799 | Common:10; Rare:101 | ||||
| chr3:119702826-119703142 | Common:6; Rare:100 | ||||
| chr3:120093874-120093979 | Common:2; Rare:49 | ||||
| chr3:120094294-120094407 | Common:1; Rare:35 | ||||
| chr3:120349266-120349513 | Common:2; Rare:89 | ||||
| chr3:120450504-120450745 | Common:1; Rare:69 | ||||
| chr3:120450966-120451114 | Rare:58 | ||||
| chr3:120596050-120596440 | Common:3; Rare:140 | ||||
| chr3:120742475-120742794 | Common:2; Rare:97 | ||||
| chr3:120907873-120908217 | Rare:76 | ||||
| chr3:120908534-120909109 | Common:2; Rare:186 | ||||
| chr3:121545915-121546124 | Common:1; Rare:60 | ||||
| chr3:121749050-121749290 | Rare:36 | ||||
| chr3:121749718-121750153 | Common:3; Rare:109 | ||||
| chr3:121834966-121835269 | Common:3; Rare:102; Clinvar:6; Clinvar (benign):2 |