| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:74098113-74098350 | Rare:44 | ||||
| chr13:74118710-74118945 | Common:1; Rare:41 | ||||
| chr13:74119928-74120171 | Common:2; Rare:45 | ||||
| chr13:74121941-74122228 | Common:1; Rare:51 | ||||
| chr13:74211103-74211288 | Rare:31 | ||||
| chr13:75608086-75608302 | Common:1; Rare:29 | ||||
| chr13:75648938-75649079 | Rare:28 | ||||
| chr13:75657279-75657395 | Common:1; Rare:21 | ||||
| chr13:75814809-75814952 | Rare:20 | ||||
| chr13:75857605-75857888 | Common:3; Rare:41 | ||||
| chr13:77021750-77022026 | Common:1; Rare:64 | ||||
| chr13:79352507-79352789 | Common:2; Rare:57 | ||||
| chr13:79383959-79384075 | Rare:25 | ||||
| chr13:79404766-79404770 | Rare:2 | ||||
| chr13:93227457-93227592 | Common:1; Rare:52; Clinvar:1; Clinvar (benign):1 |