| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:112646338-112646658 | Common:2; Rare:121; Clinvar:2 | ||||
| chr4:113761002-113761276 | Common:1; Rare:78 | ||||
| chr4:113979589-113979817 | Common:6; Rare:54 | ||||
| chr4:117085505-117085611 | Common:1; Rare:29 | ||||
| chr4:118352700-118352842 | Common:2; Rare:52; Clinvar:1; Clinvar (benign):1 | ||||
| chr4:118352941-118353237 | Rare:90 | ||||
| chr4:118685326-118685534 | Common:2; Rare:57 | ||||
| chr4:118836021-118836228 | Common:1; Rare:45 | ||||
| chr4:119212355-119212777 | Common:5; Rare:131 | ||||
| chr4:119627156-119627375 | Common:1; Rare:62 | ||||
| chr4:119627590-119627904 | Rare:52 | ||||
| chr4:119627955-119628179 | Common:3; Rare:48 | ||||
| chr4:119628561-119628988 | Common:4; Rare:173 | ||||
| chr4:120066754-120066964 | Common:4; Rare:62 | ||||
| chr4:121696582-121697093 | Common:6; Rare:127 |