| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:74038683-74038712 | Rare:4 | ||||
| chr4:74038745-74038835 | Rare:22 | ||||
| chr4:74099165-74099406 | Common:2; Rare:55 | ||||
| chr4:74158020-74158179 | Rare:74 | ||||
| chr4:74444923-74445162 | Common:1; Rare:49 | ||||
| chr4:75514273-75514514 | Common:1; Rare:83 | ||||
| chr4:75514646-75514768 | Rare:33 | ||||
| chr4:75673067-75673222 | Rare:37 | ||||
| chr4:75673307-75673648 | Common:1; Rare:137 | ||||
| chr4:75724375-75724723 | Common:1; Rare:97 | ||||
| chr4:75940045-75940354 | Common:2; Rare:93 | ||||
| chr4:76036008-76036230 | Common:2; Rare:50 | ||||
| chr4:76148364-76148594 | Common:4; Rare:70 | ||||
| chr4:76213449-76214025 | Common:5; Rare:196; Clinvar:3; Clinvar (benign):9 | ||||
| chr4:76949596-76949859 | Rare:74 |