| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:182391702-182392148 | Common:15; Rare:540; Clinvar:21; Clinvar (benign):15 | ||||
| chr1:182392102-182392590 | Common:18; Rare:312; Clinvar (benign):2 | ||||
| chr1:182588530-182589140 | Common:10; Rare:193 | ||||
| chr1:182589150-182589460 | Common:1; Rare:87 | ||||
| chr1:182604263-182604663 | Rare:242 | ||||
| chr1:182789501-182789901 | Common:12; Rare:458 | ||||
| chr1:182791500-182792176 | Common:8; Rare:194 | ||||
| chr1:182839086-182839486 | Common:7; Rare:747 | ||||
| chr1:182839460-182839840 | Common:15; Rare:614 | ||||
| chr1:182839847-182840290 | Common:8; Rare:394 | ||||
| chr1:183022973-183023373 | Common:12; Rare:186 | ||||
| chr1:183471657-183472190 | Common:6; Rare:355 | ||||
| chr1:183472206-183472571 | Common:12; Rare:594 | ||||
| chr1:183472818-183473414 | Common:15; Rare:322 | ||||
| chr1:183590380-183590707 | Common:6; Rare:108; Clinvar (benign):4 |