| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:46700034-46700144 | Rare:26 | ||||
| chr2:46831715-46831943 | Common:3; Rare:48 | ||||
| chr2:46914638-46914865 | Common:2; Rare:47 | ||||
| chr2:47043663-47043889 | Rare:50 | ||||
| chr2:47160778-47160850 | Rare:14; Clinvar (benign):1 | ||||
| chr2:47162284-47162739 | Rare:82; Clinvar (benign):4 | ||||
| chr2:47175360-47175540 | Common:1; Rare:52 | ||||
| chr2:47175662-47175946 | Common:3; Rare:103 | ||||
| chr2:47308255-47308268 | Rare:3 | ||||
| chr2:47691285-47691434 | Common:3; Rare:25 | ||||
| chr2:47795725-47795942 | Common:3; Rare:60; Clinvar:7; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr2:47801454-47801527 | Rare:20 | ||||
| chr2:47802577-47802731 | Common:1; Rare:48 | ||||
| chr2:47804721-47805025 | Common:1; Rare:121; Clinvar:26; Clinvar (benign):13; Clinvar (pathogenic):7 | ||||
| chr2:47806142-47806428 | Common:2; Rare:142; Clinvar:42; Clinvar (benign):28; Clinvar (pathogenic):9 |