| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:31042739-31042940 | Common:1; Rare:31 | ||||
| chr18:31101734-31102006 | Common:2; Rare:60; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr18:31102379-31102523 | Rare:37; Clinvar:1 | ||||
| chr18:31497793-31497889 | Rare:23 | ||||
| chr18:31497927-31498090 | Rare:36 | ||||
| chr18:31498095-31498254 | Common:1; Rare:51; Clinvar:3; Clinvar (benign):4 | ||||
| chr18:31498281-31498332 | Rare:21; Clinvar:3; Clinvar (benign):1 | ||||
| chr18:31591727-31591886 | Rare:32; Clinvar:1; Clinvar (benign):1 | ||||
| chr18:31684576-31684689 | Rare:33 | ||||
| chr18:31684703-31684864 | Rare:49 | ||||
| chr18:31685160-31685381 | Common:5; Rare:64 | ||||
| chr18:31685424-31685694 | Common:1; Rare:87 | ||||
| chr18:31685827-31686022 | Rare:58 | ||||
| chr18:31943007-31943430 | Common:7; Rare:134 | ||||
| chr18:32018805-32018978 | Common:2; Rare:58; Clinvar:3 |