| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:151089289-151089633 | Common:1; Rare:92 | ||||
| chr7:155644394-155644708 | Common:2; Rare:104 | ||||
| chr7:157336790-157337015 | Common:1; Rare:90 | ||||
| chr7:157382114-157382312 | Common:1; Rare:64; Clinvar:5 | ||||
| chr8:1755549-1755865 | Common:7; Rare:87 | ||||
| chr8:6406548-6406670 | Common:3; Rare:70; Clinvar:2; Clinvar (benign):1 | ||||
| chr8:11845732-11846031 | Common:3; Rare:175 | ||||
| chr8:11868012-11868306 | Rare:139 | ||||
| chr8:17246795-17246995 | Common:1; Rare:88 | ||||
| chr8:18084931-18085078 | Rare:29 | ||||
| chr8:20197205-20197440 | Common:1; Rare:114 | ||||
| chr8:21911908-21912232 | Common:5; Rare:99 | ||||
| chr8:22141305-22141523 | Rare:50 | ||||
| chr8:22245026-22245153 | Rare:67 | ||||
| chr8:23068979-23069172 | Common:1; Rare:77 |