| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:117520527-117520753 | Common:5; Rare:50 | ||||
| chr8:119832821-119832914 | Common:1; Rare:33 | ||||
| chr8:120445103-120445419 | Common:1; Rare:71 | ||||
| chr8:122781589-122781689 | Rare:15 | ||||
| chr8:124474156-124474274 | Common:1; Rare:21 | ||||
| chr8:124474549-124474734 | Rare:66 | ||||
| chr8:124474990-124475121 | Rare:46 | ||||
| chr8:124539048-124539206 | Common:2; Rare:83; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr8:124998221-124998512 | Common:1; Rare:116 | ||||
| chr8:125091712-125091907 | Common:2; Rare:68; Clinvar (benign):3 | ||||
| chr8:132760531-132760789 | Common:1; Rare:41 | ||||
| chr8:133075319-133075524 | Common:1; Rare:47 | ||||
| chr8:133076245-133076635 | Common:1; Rare:75 | ||||
| chr8:133297153-133297761 | Common:4; Rare:212; Clinvar:4; Clinvar (benign):1 | ||||
| chr8:133570483-133570796 | Common:1; Rare:72 |