| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:52787751-52787950 | Common:1; Rare:40 | ||||
| chr5:52989210-52989365 | Common:4; Rare:43; Clinvar (benign):1 | ||||
| chr5:53109725-53109903 | Common:1; Rare:90; Clinvar:2 | ||||
| chr5:54310507-54310712 | Rare:66 | ||||
| chr5:55307631-55308016 | Common:4; Rare:130 | ||||
| chr5:55534638-55534764 | Common:2; Rare:46 | ||||
| chr5:55534960-55535179 | Common:1; Rare:75 | ||||
| chr5:55994797-55995152 | Rare:117 | ||||
| chr5:56952098-56952315 | Rare:79 | ||||
| chr5:57173548-57173863 | Common:2; Rare:111 | ||||
| chr5:58460072-58460182 | Common:3; Rare:45 | ||||
| chr5:59768497-59768723 | Rare:57 | ||||
| chr5:59768819-59768860 | Rare:6 | ||||
| chr5:60487990-60488291 | Common:1; Rare:51 | ||||
| chr5:60700118-60700258 | Common:2; Rare:48 |