| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:3248347-3248469 | Common:1; Rare:28 | ||||
| chr18:3261792-3262249 | Common:6; Rare:145 | ||||
| chr18:3411588-3412062 | Common:4; Rare:111 | ||||
| chr18:3448433-3448496 | Rare:15 | ||||
| chr18:3449108-3449345 | Common:5; Rare:56 | ||||
| chr18:3450026-3450354 | Common:1; Rare:91 | ||||
| chr18:3454891-3455089 | Rare:36 | ||||
| chr18:7754852-7754988 | Common:1; Rare:24 | ||||
| chr18:7946865-7946931 | Rare:16 | ||||
| chr18:8705455-8705576 | Rare:32 | ||||
| chr18:8707439-8707845 | Common:3; Rare:73 | ||||
| chr18:9102501-9102795 | Common:2; Rare:121; Clinvar:6; Clinvar (benign):2 | ||||
| chr18:9136542-9137059 | Common:1; Rare:196 | ||||
| chr18:9334437-9334907 | Common:1; Rare:113 | ||||
| chr18:9474883-9475078 | Common:1; Rare:47 |