| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:118278608-118278779 | Common:4; Rare:65 | ||||
| chr4:118591553-118591839 | Common:4; Rare:94 | ||||
| chr4:119026405-119026630 | Rare:31 | ||||
| chr4:119217394-119217671 | Common:2; Rare:35 | ||||
| chr4:119268089-119268407 | Common:5; Rare:76; Clinvar:1 | ||||
| chr4:119454556-119454969 | Common:18; Rare:132 | ||||
| chr4:147733582-147733940 | Common:1; Rare:63 | ||||
| chr4:151176556-151176890 | Common:1; Rare:37 | ||||
| chr4:151185224-151185277 | Common:1; Rare:12 | ||||
| chr4:153684143-153684293 | Common:1; Rare:50 | ||||
| chr4:158059500-158059574 | Rare:11 | ||||
| chr4:168890791-168891007 | Common:1; Rare:57; Clinvar:3; Clinvar (benign):1 | ||||
| chr4:168924017-168924418 | Rare:97; Clinvar:4; Clinvar (benign):1 | ||||
| chr4:184824417-184824692 | Common:2; Rare:56 | ||||
| chr4:186693552-186693840 | Rare:49 |