| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:33285719-33285954 | Common:1; Rare:55 | ||||
| chr13:34942171-34942298 | Common:3; Rare:39 | ||||
| chr13:35476307-35476415 | Rare:22 | ||||
| chr13:35476604-35476869 | Common:1; Rare:47 | ||||
| chr13:36346271-36346454 | Common:2; Rare:48; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:36673869-36674031 | Common:1; Rare:53 | ||||
| chr13:37059596-37059751 | Common:1; Rare:52 | ||||
| chr13:37598710-37598811 | Common:2; Rare:26 | ||||
| chr13:38349536-38349869 | Common:4; Rare:96; Clinvar (pathogenic):1 | ||||
| chr13:38350242-38350353 | Rare:35 | ||||
| chr13:39038087-39038422 | Common:1; Rare:86 | ||||
| chr13:41061203-41061580 | Common:3; Rare:130 | ||||
| chr13:44435159-44435454 | Common:3; Rare:85 | ||||
| chr13:44436823-44436997 | Common:2; Rare:55 | ||||
| chr13:44989456-44989597 | Rare:49 |