| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:21600655-21600931 | Common:2; Rare:74 | ||||
| chr18:21704718-21704984 | Rare:80 | ||||
| chr18:22168780-22169144 | Common:5; Rare:81 | ||||
| chr18:22169321-22169595 | Common:2; Rare:73 | ||||
| chr18:22933267-22933446 | Common:2; Rare:70; Clinvar:4; Clinvar (benign):2 | ||||
| chr18:22933807-22933889 | Common:1; Rare:31 | ||||
| chr18:23453176-23453340 | Rare:57 | ||||
| chr18:23503291-23503547 | Common:2; Rare:94 | ||||
| chr18:23586415-23586526 | Common:2; Rare:54; Clinvar:3; Clinvar (benign):1 | ||||
| chr18:23872950-23873031 | Rare:26 | ||||
| chr18:24397778-24398102 | Common:2; Rare:115 | ||||
| chr18:24426600-24426765 | Common:3; Rare:66 | ||||
| chr18:25352092-25352473 | Common:2; Rare:154 | ||||
| chr18:26549421-26549611 | Common:1; Rare:35 | ||||
| chr18:31498082-31498259 | Common:1; Rare:57; Clinvar:4; Clinvar (benign):5 |