| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:24512739-24512843 | Common:3; Rare:31 | ||||
| chr13:24922795-24923067 | Common:2; Rare:86; Clinvar:1 | ||||
| chr13:25301478-25301686 | Common:1; Rare:82 | ||||
| chr13:27251251-27251617 | Common:5; Rare:109 | ||||
| chr13:27450136-27450210 | Common:2; Rare:20 | ||||
| chr13:28658978-28659180 | Rare:96; Clinvar (pathogenic):1 | ||||
| chr13:30307001-30307224 | Common:4; Rare:59 | ||||
| chr13:30465795-30466140 | Common:1; Rare:111 | ||||
| chr13:30617520-30618040 | Common:1; Rare:169 | ||||
| chr13:32315397-32315552 | Common:1; Rare:46; Clinvar:2; Clinvar (benign):2 | ||||
| chr13:40789347-40789621 | Common:2; Rare:93; Clinvar:5; Clinvar (benign):2 | ||||
| chr13:41061387-41061594 | Common:2; Rare:57 | ||||
| chr13:43879466-43879624 | Rare:43 | ||||
| chr13:43879743-43879854 | Common:15; Rare:43 | ||||
| chr13:44436808-44437017 | Common:2; Rare:65 |