| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:82860238-82860380 | Common:2; Rare:30 | ||||
| chr17:82926241-82926477 | Common:3; Rare:66 | ||||
| chr17:83048546-83048719 | Rare:64 | ||||
| chr17:83051764-83052027 | Common:8; Rare:90 | ||||
| chr18:268015-268113 | Common:1; Rare:33 | ||||
| chr18:812209-812431 | Common:2; Rare:78 | ||||
| chr18:812517-812628 | Common:1; Rare:29 | ||||
| chr18:812741-812930 | Rare:50 | ||||
| chr18:2571237-2571597 | Common:5; Rare:96 | ||||
| chr18:2655533-2655737 | Common:4; Rare:99 | ||||
| chr18:2655834-2656145 | Common:4; Rare:109; Clinvar:5; Clinvar (benign):1 | ||||
| chr18:2982808-2983169 | Common:3; Rare:61 | ||||
| chr18:3247256-3247734 | Common:4; Rare:131 | ||||
| chr18:3247747-3247925 | Rare:65 | ||||
| chr18:3261815-3262236 | Common:6; Rare:133 |