| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:155667259-155667415 | Rare:38 | ||||
| chr4:156971123-156971211 | Rare:11 | ||||
| chr4:157219873-157220180 | Rare:71 | ||||
| chr4:157220260-157220335 | Rare:13 | ||||
| chr4:157220446-157221089 | Common:7; Rare:173 | ||||
| chr4:157221139-157221438 | Common:1; Rare:53 | ||||
| chr4:158671711-158672425 | Common:7; Rare:199; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:158723150-158723465 | Common:2; Rare:136 | ||||
| chr4:158768854-158769215 | Common:1; Rare:121 | ||||
| chr4:159103805-159104165 | Common:4; Rare:128 | ||||
| chr4:159267072-159267185 | Rare:17 | ||||
| chr4:159267413-159267535 | Rare:18 | ||||
| chr4:162163927-162164133 | Common:1; Rare:49 | ||||
| chr4:163166832-163166994 | Common:2; Rare:58 | ||||
| chr4:163494343-163494771 | Common:3; Rare:168 |