| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:107824769-107825035 | Common:1; Rare:73 | ||||
| chr4:107989661-107990031 | Common:6; Rare:156; Clinvar:5; Clinvar (benign):5 | ||||
| chr4:108620378-108620640 | Common:6; Rare:132 | ||||
| chr4:109433756-109433948 | Common:1; Rare:63 | ||||
| chr4:109560082-109560363 | Common:5; Rare:81 | ||||
| chr4:109815479-109815553 | Rare:23 | ||||
| chr4:112145293-112145469 | Common:1; Rare:43 | ||||
| chr4:112231586-112231852 | Common:2; Rare:82 | ||||
| chr4:112232174-112232251 | Rare:33 | ||||
| chr4:112285851-112285978 | Rare:40 | ||||
| chr4:112636886-112637204 | Common:2; Rare:87 | ||||
| chr4:112637394-112637570 | Common:3; Rare:47 | ||||
| chr4:113761102-113761248 | Common:1; Rare:40 | ||||
| chr4:118685286-118685566 | Common:3; Rare:81 | ||||
| chr4:119212312-119212807 | Common:5; Rare:151 |