| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:49996735-49997124 | Common:1; Rare:86 | ||||
| chr13:50081992-50082318 | Common:1; Rare:94 | ||||
| chr13:51453013-51453388 | Rare:146 | ||||
| chr13:51804105-51804254 | Common:2; Rare:46 | ||||
| chr13:52012128-52012424 | Common:2; Rare:95; Clinvar:1 | ||||
| chr13:52406132-52406416 | Common:2; Rare:82 | ||||
| chr13:52450596-52450684 | Rare:25 | ||||
| chr13:52455329-52455501 | Common:3; Rare:57 | ||||
| chr13:52652655-52652933 | Common:3; Rare:92 | ||||
| chr13:72727579-72727950 | Common:6; Rare:137 | ||||
| chr13:72781836-72782188 | Common:1; Rare:135 | ||||
| chr13:75481449-75481730 | Common:2; Rare:120; Clinvar:1; Clinvar (benign):2 | ||||
| chr13:76991925-76992220 | Common:4; Rare:137; Clinvar:23; Clinvar (benign):19; Clinvar (pathogenic):3 | ||||
| chr13:77027142-77027287 | Common:5; Rare:43 | ||||
| chr13:77918685-77918881 | Common:1; Rare:40 |