| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:119211988-119212763 | Common:32; Rare:954 | ||||
| chr4:119213000-119213450 | Rare:149 | ||||
| chr4:119300423-119301051 | Common:11; Rare:1214 | ||||
| chr4:120065978-120067099 | Common:32; Rare:851 | ||||
| chr4:120067040-120067777 | Common:22; Rare:401 | ||||
| chr4:121696081-121696522 | Common:12; Rare:147 | ||||
| chr4:121696868-121697268 | Common:22; Rare:346 | ||||
| chr4:121800880-121801460 | Common:20; Rare:662 | ||||
| chr4:121823158-121823807 | Common:1; Rare:259 | ||||
| chr4:121823749-121824212 | Common:15; Rare:475 | ||||
| chr4:121870356-121870756 | Common:5; Rare:362; Clinvar (benign):5 | ||||
| chr4:121951459-121952323 | Common:5; Rare:307 | ||||
| chr4:122152000-122152610 | Common:14; Rare:714 | ||||
| chr4:122732339-122732822 | Common:17; Rare:752; Clinvar:14; Clinvar (benign):10 | ||||
| chr4:122732836-122733236 | Common:1; Rare:70 |