| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:82735232-82735291 | Common:1; Rare:14 | ||||
| chr17:82751976-82752176 | Common:1; Rare:85 | ||||
| chr17:83051745-83052045 | Common:9; Rare:104 | ||||
| chr18:158401-158704 | Rare:102 | ||||
| chr18:267971-268123 | Common:1; Rare:58 | ||||
| chr18:657495-657749 | Common:8; Rare:79 | ||||
| chr18:657753-657996 | Common:1; Rare:62 | ||||
| chr18:658250-658449 | Common:4; Rare:41 | ||||
| chr18:712518-712829 | Common:3; Rare:125 | ||||
| chr18:812117-812632 | Common:5; Rare:182 | ||||
| chr18:2571225-2571650 | Common:6; Rare:106 | ||||
| chr18:2655580-2655996 | Common:5; Rare:159 | ||||
| chr18:2656032-2656228 | Common:3; Rare:72; Clinvar:7; Clinvar (benign):1 | ||||
| chr18:3247204-3247614 | Common:5; Rare:111 | ||||
| chr18:3247736-3247935 | Rare:67 |