| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:119212987-119213108 | Common:1; Rare:24 | ||||
| chr4:119213120-119213336 | Rare:30 | ||||
| chr4:119300490-119300928 | Common:2; Rare:194 | ||||
| chr4:119628043-119628102 | Rare:16 | ||||
| chr4:120066833-120066973 | Common:4; Rare:32 | ||||
| chr4:121696862-121697139 | Common:5; Rare:76 | ||||
| chr4:121801246-121801405 | Common:2; Rare:51 | ||||
| chr4:122152214-122152527 | Common:2; Rare:115 | ||||
| chr4:122732425-122732768 | Common:1; Rare:106; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:122827259-122827332 | Rare:26 | ||||
| chr4:122922933-122923147 | Common:2; Rare:69; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr4:123396681-123396843 | Rare:42 | ||||
| chr4:124712649-124712968 | Common:1; Rare:101 | ||||
| chr4:127880764-127880934 | Rare:61 | ||||
| chr4:128060979-128061357 | Common:1; Rare:137 |