| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:50081980-50082262 | Common:1; Rare:78 | ||||
| chr13:50715485-50715690 | Rare:47 | ||||
| chr13:50909959-50910074 | Rare:27; Clinvar:1 | ||||
| chr13:51453013-51453388 | Rare:146 | ||||
| chr13:51804099-51804305 | Common:2; Rare:59 | ||||
| chr13:52012105-52012435 | Common:2; Rare:110; Clinvar:1 | ||||
| chr13:52406125-52406291 | Common:2; Rare:40 | ||||
| chr13:52455344-52455490 | Common:3; Rare:46 | ||||
| chr13:52652404-52652817 | Common:1; Rare:104 | ||||
| chr13:60397110-60397354 | Common:4; Rare:94 | ||||
| chr13:72727598-72727950 | Common:4; Rare:129 | ||||
| chr13:72781853-72782188 | Common:1; Rare:130 | ||||
| chr13:75635769-75635890 | Common:1; Rare:31 | ||||
| chr13:75636033-75636347 | Common:2; Rare:70 | ||||
| chr13:76992043-76992207 | Common:1; Rare:76; Clinvar:10; Clinvar (benign):8; Clinvar (pathogenic):3 |