| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:110308332-110308422 | Common:2; Rare:19 | ||||
| chr13:110308510-110308622 | Common:1; Rare:22 | ||||
| chr13:110340894-110341238 | Common:3; Rare:81 | ||||
| chr13:110343307-110343381 | Rare:16 | ||||
| chr13:110388286-110388461 | Common:2; Rare:34 | ||||
| chr13:110397173-110397241 | Rare:11 | ||||
| chr13:110424724-110425009 | Common:4; Rare:80; Clinvar:3; Clinvar (benign):2 | ||||
| chr13:110503841-110504264 | Common:4; Rare:142; Clinvar:1; Clinvar (benign):4 | ||||
| chr13:111189285-111189358 | Rare:14 | ||||
| chr13:112996927-112997081 | Common:1; Rare:43 | ||||
| chr13:113139177-113139469 | Rare:74; Clinvar:2 | ||||
| chr13:113480703-113480896 | Rare:49 | ||||
| chr13:113493468-113493629 | Common:4; Rare:22 | ||||
| chr13:113650409-113650579 | Rare:52 | ||||
| chr13:113651602-113651770 | Rare:68 |