| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:165112815-165113022 | Common:1; Rare:60 | ||||
| chr4:165207461-165207692 | Common:4; Rare:169 | ||||
| chr4:165327318-165327759 | Common:6; Rare:254 | ||||
| chr4:165328160-165328450 | Common:4; Rare:54 | ||||
| chr4:165874640-165875040 | Common:2; Rare:179 | ||||
| chr4:168318230-168318630 | Common:12; Rare:141 | ||||
| chr4:168318685-168318810 | Rare:29 | ||||
| chr4:168480365-168480542 | Common:1; Rare:34 | ||||
| chr4:168480650-168480980 | Common:2; Rare:111 | ||||
| chr4:168631332-168631857 | Common:2; Rare:221 | ||||
| chr4:168831850-168832126 | Common:5; Rare:129 | ||||
| chr4:169010132-169010468 | Common:5; Rare:174 | ||||
| chr4:169270915-169271068 | Common:1; Rare:53 | ||||
| chr4:169612421-169612783 | Common:10; Rare:157; Clinvar:9; Clinvar (benign):4 | ||||
| chr4:169620267-169620737 | Common:4; Rare:295 |