| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:44989443-44989607 | Rare:62 | ||||
| chr13:45341040-45341609 | Common:4; Rare:258 | ||||
| chr13:45418340-45418516 | Rare:49 | ||||
| chr13:45464753-45465022 | Common:1; Rare:68 | ||||
| chr13:46052709-46052850 | Common:2; Rare:36 | ||||
| chr13:48001253-48001376 | Common:1; Rare:57; Clinvar:3; Clinvar (benign):3 | ||||
| chr13:48037645-48037783 | Common:1; Rare:66 | ||||
| chr13:49247830-49247964 | Rare:38 | ||||
| chr13:49444005-49444299 | Common:1; Rare:102 | ||||
| chr13:49495957-49496063 | Rare:29 | ||||
| chr13:49585516-49585612 | Common:1; Rare:29 | ||||
| chr13:49792530-49792706 | Common:4; Rare:70 | ||||
| chr13:49996735-49997053 | Common:1; Rare:57 | ||||
| chr13:50081992-50082267 | Common:1; Rare:79 | ||||
| chr13:51453013-51453346 | Rare:117 |