| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:50081966-50082262 | Common:1; Rare:83 | ||||
| chr13:50715471-50715690 | Rare:50 | ||||
| chr13:50909833-50910074 | Common:1; Rare:53; Clinvar:4; Clinvar (benign):1 | ||||
| chr13:51452666-51452756 | Rare:23 | ||||
| chr13:51453013-51453388 | Rare:146 | ||||
| chr13:51803701-51803836 | Rare:40 | ||||
| chr13:51804082-51804244 | Common:2; Rare:49 | ||||
| chr13:52012106-52012433 | Common:2; Rare:109; Clinvar:1 | ||||
| chr13:52159558-52159649 | Common:1; Rare:18 | ||||
| chr13:52450580-52450726 | Rare:44 | ||||
| chr13:52455344-52455543 | Common:3; Rare:75 | ||||
| chr13:52652372-52652714 | Rare:91 | ||||
| chr13:60397173-60397391 | Common:4; Rare:79 | ||||
| chr13:72727587-72727943 | Common:5; Rare:132 | ||||
| chr13:72781853-72782188 | Common:1; Rare:130 |