| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:37000775-37000800 | Rare:14 | ||||
| chr13:37059585-37059726 | Common:1; Rare:49 | ||||
| chr13:37869725-37870037 | Common:1; Rare:82 | ||||
| chr13:38349548-38349911 | Common:3; Rare:122; Clinvar (pathogenic):1 | ||||
| chr13:38350242-38350408 | Rare:51 | ||||
| chr13:39038346-39038456 | Rare:30 | ||||
| chr13:40771138-40771268 | Common:1; Rare:45 | ||||
| chr13:40982858-40983029 | Common:3; Rare:27 | ||||
| chr13:41060889-41060950 | Common:13; Rare:44 | ||||
| chr13:41061179-41061586 | Common:3; Rare:138 | ||||
| chr13:41132707-41132949 | Rare:60 | ||||
| chr13:42271760-42272046 | Common:2; Rare:81 | ||||
| chr13:43023559-43023633 | Common:1; Rare:34 | ||||
| chr13:43879476-43879558 | Rare:23 | ||||
| chr13:43879707-43879875 | Common:18; Rare:56 |