| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:26320612-26320832 | Common:1; Rare:90 | ||||
| chr4:26320905-26321057 | Rare:55; Clinvar (benign):1 | ||||
| chr4:26860563-26860667 | Rare:35 | ||||
| chr4:30720237-30720432 | Common:1; Rare:50 | ||||
| chr4:37826544-37826735 | Common:6; Rare:70 | ||||
| chr4:37977208-37977482 | Rare:65 | ||||
| chr4:39182328-39182554 | Common:1; Rare:52; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:39366324-39366417 | Rare:29 | ||||
| chr4:39458857-39459112 | Common:3; Rare:147; Clinvar (benign):5 | ||||
| chr4:39527354-39527789 | Common:3; Rare:115 | ||||
| chr4:39527929-39527992 | Rare:12 | ||||
| chr4:39638823-39639181 | Common:1; Rare:132 | ||||
| chr4:39697986-39698203 | Common:1; Rare:89 | ||||
| chr4:40056645-40057010 | Common:4; Rare:108 | ||||
| chr4:40629769-40629917 | Common:1; Rare:43 |