| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:124474190-124474263 | Common:1; Rare:18 | ||||
| chr8:124474512-124474797 | Common:1; Rare:105 | ||||
| chr8:124474966-124475137 | Rare:62 | ||||
| chr8:124538975-124539284 | Common:2; Rare:160; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr8:124998243-124998527 | Common:1; Rare:117 | ||||
| chr8:125091699-125091931 | Common:2; Rare:82; Clinvar:1; Clinvar (benign):3 | ||||
| chr8:125430030-125430421 | Common:2; Rare:87 | ||||
| chr8:127735911-127736623 | Common:4; Rare:186 | ||||
| chr8:130443464-130443777 | Common:5; Rare:85 | ||||
| chr8:132675523-132675665 | Rare:44 | ||||
| chr8:133297177-133297525 | Common:3; Rare:141; Clinvar:4; Clinvar (benign):1 | ||||
| chr8:133571855-133572352 | Common:1; Rare:127 | ||||
| chr8:140511228-140511558 | Common:3; Rare:126 | ||||
| chr8:140511612-140511643 | Rare:7 | ||||
| chr8:140511940-140511997 | Common:1; Rare:27 |