| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:3292721-3293065 | Common:3; Rare:137 | ||||
| chr4:4290049-4290220 | Common:3; Rare:65 | ||||
| chr4:4541974-4542115 | Common:1; Rare:63 | ||||
| chr4:6640545-6640716 | Common:2; Rare:69 | ||||
| chr4:6987034-6987219 | Common:1; Rare:49 | ||||
| chr4:15681532-15681854 | Common:3; Rare:115 | ||||
| chr4:17810677-17811003 | Common:2; Rare:100 | ||||
| chr4:26860433-26860845 | Common:5; Rare:136 | ||||
| chr4:39458844-39459075 | Common:3; Rare:127; Clinvar (benign):1 | ||||
| chr4:39527400-39527744 | Common:2; Rare:83 | ||||
| chr4:39638960-39639125 | Rare:75 | ||||
| chr4:39697969-39698195 | Common:1; Rare:91 | ||||
| chr4:52659219-52659407 | Common:1; Rare:68 | ||||
| chr4:56435516-56435801 | Common:4; Rare:89 | ||||
| chr4:56467573-56467660 | Common:2; Rare:37; Clinvar (benign):4 |