| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:25312648-25312887 | Common:2; Rare:94 | ||||
| chr4:25914051-25914358 | Common:3; Rare:131 | ||||
| chr4:26320905-26321046 | Rare:51; Clinvar (benign):1 | ||||
| chr4:37826571-37826729 | Common:1; Rare:57 | ||||
| chr4:37977195-37977463 | Rare:66 | ||||
| chr4:38867622-38867821 | Common:2; Rare:74 | ||||
| chr4:39182202-39182554 | Common:1; Rare:79; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:39458857-39459122 | Common:3; Rare:153; Clinvar:1; Clinvar (benign):5 | ||||
| chr4:39527388-39527781 | Common:2; Rare:104 | ||||
| chr4:39638805-39639149 | Common:1; Rare:122 | ||||
| chr4:39698018-39698185 | Common:1; Rare:70 | ||||
| chr4:40629762-40630094 | Common:1; Rare:84 | ||||
| chr4:40630130-40630250 | Common:1; Rare:19 | ||||
| chr4:40630592-40630783 | Common:1; Rare:43 | ||||
| chr4:41359511-41359630 | Rare:19 |