| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:48001253-48001410 | Common:1; Rare:72; Clinvar:3; Clinvar (benign):3 | ||||
| chr13:48037405-48037767 | Common:2; Rare:136 | ||||
| chr13:48233066-48233475 | Common:3; Rare:143 | ||||
| chr13:48492772-48492907 | Common:1; Rare:23 | ||||
| chr13:48533038-48533071 | Common:1; Rare:12 | ||||
| chr13:49247823-49247976 | Rare:48 | ||||
| chr13:49444005-49444476 | Common:1; Rare:152 | ||||
| chr13:49495894-49496047 | Rare:32 | ||||
| chr13:49936248-49936592 | Common:1; Rare:105 | ||||
| chr13:49996785-49997092 | Common:1; Rare:57 | ||||
| chr13:50081952-50082264 | Common:1; Rare:87 | ||||
| chr13:51453013-51453346 | Rare:117 | ||||
| chr13:51804094-51804208 | Common:2; Rare:40 | ||||
| chr13:52012106-52012428 | Common:2; Rare:104; Clinvar:1 | ||||
| chr13:52455344-52455507 | Common:3; Rare:53 |