| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:48533038-48533116 | Common:2; Rare:24 | ||||
| chr13:48975800-48975928 | Rare:48 | ||||
| chr13:48976544-48976824 | Common:1; Rare:82 | ||||
| chr13:49247807-49247990 | Rare:53 | ||||
| chr13:49444005-49444476 | Common:1; Rare:152 | ||||
| chr13:49585527-49585633 | Common:1; Rare:34 | ||||
| chr13:49792508-49792674 | Common:5; Rare:78 | ||||
| chr13:49936231-49936588 | Common:1; Rare:111 | ||||
| chr13:49996785-49997145 | Common:1; Rare:75 | ||||
| chr13:50081976-50082290 | Common:1; Rare:84 | ||||
| chr13:50909854-50910074 | Common:1; Rare:49; Clinvar:3; Clinvar (benign):1 | ||||
| chr13:51453013-51453388 | Rare:146 | ||||
| chr13:51804084-51804227 | Common:2; Rare:44 | ||||
| chr13:52012110-52012421 | Common:2; Rare:101; Clinvar:1 | ||||
| chr13:52455323-52455507 | Common:3; Rare:59 |