| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:49997000-49997128 | Rare:40 | ||||
| chr13:50081948-50082298 | Common:1; Rare:97 | ||||
| chr13:50909615-50910421 | Common:3; Rare:199; Clinvar:7; Clinvar (benign):1 | ||||
| chr13:51453013-51453389 | Rare:146 | ||||
| chr13:51804156-51804221 | Rare:18 | ||||
| chr13:52012123-52012448 | Common:2; Rare:119; Clinvar:1 | ||||
| chr13:52415946-52416025 | Rare:16 | ||||
| chr13:52450502-52450698 | Common:1; Rare:64 | ||||
| chr13:52455301-52455610 | Common:3; Rare:114 | ||||
| chr13:52652386-52652958 | Common:3; Rare:172 | ||||
| chr13:52653137-52653198 | Common:1; Rare:17 | ||||
| chr13:60163762-60164118 | Common:2; Rare:92 | ||||
| chr13:60397319-60397405 | Common:2; Rare:34 | ||||
| chr13:67229777-67229963 | Rare:28 | ||||
| chr13:67230240-67230666 | Common:2; Rare:130 |