| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:63752837-63753057 | Rare:39 | ||||
| chr18:63949140-63949421 | Common:1; Rare:90 | ||||
| chr18:63969965-63970330 | Common:7; Rare:71 | ||||
| chr18:63970371-63970730 | Common:4; Rare:82 | ||||
| chr18:63970814-63971118 | Common:2; Rare:73 | ||||
| chr18:65750882-65751015 | Rare:46 | ||||
| chr18:67516625-67517274 | Common:7; Rare:160 | ||||
| chr18:68714527-68714726 | Common:1; Rare:58 | ||||
| chr18:68714916-68715291 | Common:7; Rare:158 | ||||
| chr18:68798053-68798132 | Rare:14 | ||||
| chr18:69400734-69401029 | Common:4; Rare:94 | ||||
| chr18:70205623-70205879 | Common:3; Rare:103; Clinvar (benign):2 | ||||
| chr18:70205957-70206089 | Rare:47 | ||||
| chr18:70288436-70288548 | Common:1; Rare:28 | ||||
| chr18:70288633-70288697 | Common:1; Rare:13 |