| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:151080984-151081170 | Common:1; Rare:60 | ||||
| chr5:151157694-151157898 | Common:1; Rare:50 | ||||
| chr5:153490489-153490738 | Rare:55 | ||||
| chr5:153490951-153491200 | Common:1; Rare:62 | ||||
| chr5:154038887-154039026 | Rare:47 | ||||
| chr5:154858467-154858722 | Common:1; Rare:82 | ||||
| chr5:154938186-154938252 | Rare:20 | ||||
| chr5:154941038-154941107 | Rare:31 | ||||
| chr5:157266050-157266177 | Rare:39 | ||||
| chr5:157858959-157859240 | Common:2; Rare:91 | ||||
| chr5:159263201-159263330 | Common:1; Rare:43 | ||||
| chr5:160008979-160009190 | Common:1; Rare:49 | ||||
| chr5:160419037-160419181 | Common:2; Rare:53 | ||||
| chr5:161547533-161547578 | Rare:9 | ||||
| chr5:161847914-161848272 | Rare:61; Clinvar:2; Clinvar (benign):5 |