| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:48037914-48038100 | Common:5; Rare:62 | ||||
| chr13:48233053-48233475 | Common:3; Rare:146 | ||||
| chr13:48303674-48304048 | Common:1; Rare:122; Clinvar:15; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr13:48492536-48492777 | Common:2; Rare:60 | ||||
| chr13:48492782-48492808 | Rare:2 | ||||
| chr13:48532722-48532864 | Common:2; Rare:53 | ||||
| chr13:48533038-48533128 | Common:2; Rare:30 | ||||
| chr13:48975668-48976109 | Common:2; Rare:133 | ||||
| chr13:48976144-48976163 | Rare:7 | ||||
| chr13:48976541-48976870 | Common:1; Rare:95 | ||||
| chr13:49247540-49247999 | Common:2; Rare:99 | ||||
| chr13:49443997-49444534 | Common:2; Rare:168 | ||||
| chr13:49495875-49496076 | Rare:48 | ||||
| chr13:49521972-49522228 | Common:2; Rare:71 | ||||
| chr13:49585471-49585640 | Common:1; Rare:58 |