| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:46797098-46797364 | Common:3; Rare:87 | ||||
| chr13:48001253-48001373 | Common:1; Rare:55; Clinvar:3; Clinvar (benign):3 | ||||
| chr13:48037592-48037767 | Rare:71 | ||||
| chr13:48037904-48038116 | Common:5; Rare:68 | ||||
| chr13:48975802-48975923 | Rare:44 | ||||
| chr13:49247823-49247968 | Rare:44 | ||||
| chr13:49444005-49444328 | Common:1; Rare:107 | ||||
| chr13:49495941-49495981 | Rare:8 | ||||
| chr13:49585527-49585612 | Common:1; Rare:26 | ||||
| chr13:49792530-49792712 | Common:4; Rare:70 | ||||
| chr13:49996715-49997086 | Common:1; Rare:84 | ||||
| chr13:50081969-50082283 | Common:1; Rare:85 | ||||
| chr13:50185564-50185924 | Common:6; Rare:66 | ||||
| chr13:50909706-50910067 | Common:1; Rare:79; Clinvar:5; Clinvar (benign):1 | ||||
| chr13:51453023-51453385 | Rare:140 |