| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:49443996-49444534 | Common:2; Rare:168 | ||||
| chr13:49445146-49445317 | Common:1; Rare:35 | ||||
| chr13:49495875-49496033 | Rare:36 | ||||
| chr13:49585491-49585658 | Common:1; Rare:61 | ||||
| chr13:49792504-49792764 | Common:5; Rare:110 | ||||
| chr13:49793048-49793131 | Common:2; Rare:23 | ||||
| chr13:49936236-49936567 | Common:1; Rare:100 | ||||
| chr13:49996719-49997124 | Common:1; Rare:94 | ||||
| chr13:50081562-50081814 | Common:1; Rare:57 | ||||
| chr13:50081933-50082317 | Common:1; Rare:108 | ||||
| chr13:50909689-50910139 | Common:1; Rare:103; Clinvar:6; Clinvar (benign):1 | ||||
| chr13:51453019-51453403 | Common:1; Rare:148 | ||||
| chr13:51584248-51584522 | Common:3; Rare:93 | ||||
| chr13:51804097-51804268 | Common:2; Rare:54 | ||||
| chr13:52012093-52012428 | Common:2; Rare:110; Clinvar:1 |