| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:45341040-45341525 | Common:4; Rare:233 | ||||
| chr13:46052557-46052819 | Common:2; Rare:67 | ||||
| chr13:46387203-46387352 | Rare:37 | ||||
| chr13:48001238-48001410 | Common:1; Rare:79; Clinvar:3; Clinvar (benign):4 | ||||
| chr13:48037683-48037789 | Common:1; Rare:57 | ||||
| chr13:48037920-48038187 | Common:5; Rare:77 | ||||
| chr13:48233085-48233406 | Rare:108 | ||||
| chr13:48233434-48233475 | Common:2; Rare:15 | ||||
| chr13:48303674-48304000 | Common:1; Rare:113; Clinvar:11; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr13:48533050-48533102 | Rare:17 | ||||
| chr13:48975780-48975923 | Common:1; Rare:51 | ||||
| chr13:48976147-48976238 | Rare:24 | ||||
| chr13:48976794-48976831 | Rare:8 | ||||
| chr13:49247807-49247994 | Rare:55 | ||||
| chr13:49444010-49444476 | Common:1; Rare:151 |