| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:112817930-112818242 | Rare:48 | ||||
| chr4:113293212-113293475 | Common:1; Rare:60; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:113761135-113761283 | Common:1; Rare:34 | ||||
| chr4:113979569-113979740 | Common:1; Rare:41 | ||||
| chr4:118685339-118685463 | Common:2; Rare:40 | ||||
| chr4:118836043-118836227 | Common:1; Rare:42 | ||||
| chr4:118888733-118888981 | Common:1; Rare:64 | ||||
| chr4:119212355-119212812 | Common:5; Rare:136 | ||||
| chr4:119213010-119213112 | Rare:23 | ||||
| chr4:119300724-119300922 | Common:1; Rare:64 | ||||
| chr4:120066784-120066973 | Common:4; Rare:52 | ||||
| chr4:120922637-120922994 | Common:1; Rare:104; Clinvar:5; Clinvar (benign):1 | ||||
| chr4:121072201-121072447 | Rare:61 | ||||
| chr4:121696850-121697139 | Common:5; Rare:78 | ||||
| chr4:121801245-121801411 | Common:2; Rare:54 |