| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:134372158-134373006 | Common:11; Rare:194 | ||||
| chr3:134373209-134373379 | Common:1; Rare:38 | ||||
| chr3:134373568-134374197 | Common:1; Rare:246 | ||||
| chr3:134374227-134374770 | Common:8; Rare:363 | ||||
| chr3:134374830-134375235 | Common:10; Rare:160 | ||||
| chr3:134484861-134485317 | Common:2; Rare:116 | ||||
| chr3:134485571-134486477 | Common:18; Rare:607 | ||||
| chr3:135965497-135965852 | Common:2; Rare:249 | ||||
| chr3:135965810-135966275 | Common:8; Rare:267 | ||||
| chr3:136194553-136195269 | Common:2; Rare:281; Clinvar:2 | ||||
| chr3:136195264-136195546 | Rare:135 | ||||
| chr3:136195720-136196049 | Common:6; Rare:339 | ||||
| chr3:136196190-136197036 | Common:5; Rare:750 | ||||
| chr3:136197133-136197271 | Rare:33 | ||||
| chr3:136250190-136250409 | Common:8; Rare:199; Clinvar:10; Clinvar (benign):10; Clinvar (pathogenic):5 |