| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:23579130-23579432 | Common:16; Rare:266 | ||||
| chr13:23888571-23888932 | Common:1; Rare:81 | ||||
| chr13:23889190-23889586 | Common:3; Rare:336 | ||||
| chr13:23979640-23979824 | Common:4; Rare:62 | ||||
| chr13:24160054-24160940 | Common:9; Rare:389 | ||||
| chr13:24512290-24512650 | Common:6; Rare:147 | ||||
| chr13:24512660-24512950 | Common:10; Rare:174 | ||||
| chr13:24680210-24680680 | Common:3; Rare:114 | ||||
| chr13:24922715-24923187 | Common:7; Rare:388; Clinvar:3; Clinvar (benign):1 | ||||
| chr13:25287248-25287637 | Common:5; Rare:197 | ||||
| chr13:25301438-25301760 | Common:5; Rare:295 | ||||
| chr13:26221420-26221710 | Common:3; Rare:84 | ||||
| chr13:26221685-26222067 | Common:2; Rare:253 | ||||
| chr13:26222106-26222638 | Common:14; Rare:240 | ||||
| chr13:26254061-26254358 | Common:3; Rare:188 |