| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:30307407-30307463 | Common:1; Rare:22 | ||||
| chr13:30617577-30618040 | Common:1; Rare:141 | ||||
| chr13:30735387-30735597 | Common:2; Rare:43 | ||||
| chr13:32031570-32031777 | Common:1; Rare:57 | ||||
| chr13:32315445-32315538 | Rare:31; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:32428096-32428224 | Rare:28 | ||||
| chr13:33205966-33206213 | Rare:50 | ||||
| chr13:33285677-33285836 | Rare:32 | ||||
| chr13:36346301-36346457 | Common:2; Rare:41; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:37000736-37000805 | Rare:27 | ||||
| chr13:38349803-38349906 | Common:1; Rare:54 | ||||
| chr13:38350208-38350341 | Rare:48 | ||||
| chr13:39038079-39038429 | Common:1; Rare:88 | ||||
| chr13:39655460-39655802 | Common:4; Rare:148; Clinvar:3; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr13:40771129-40771264 | Common:1; Rare:48 |