| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:144444367-144444606 | Common:1; Rare:131 | ||||
| chr8:144465303-144465516 | Common:8; Rare:145 | ||||
| chr8:144465650-144466090 | Common:1; Rare:62 | ||||
| chr8:144477773-144478120 | Common:13; Rare:240 | ||||
| chr8:144500809-144501200 | Rare:296 | ||||
| chr8:144501200-144501510 | Rare:200 | ||||
| chr8:144503210-144503720 | Common:4; Rare:199 | ||||
| chr8:144508509-144508909 | Common:4; Rare:151 | ||||
| chr8:144508940-144509151 | Rare:125 | ||||
| chr8:144517732-144518050 | Common:2; Rare:204; Clinvar:10; Clinvar (benign):1 | ||||
| chr8:144528904-144529202 | Common:4; Rare:245 | ||||
| chr8:144755244-144755692 | Common:2; Rare:244 | ||||
| chr8:144792275-144792612 | Common:6; Rare:220 | ||||
| chr8:144798789-144799042 | Common:4; Rare:149 | ||||
| chr8:144827153-144827620 | Common:8; Rare:260 |