| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:55519334-55519779 | Common:6; Rare:658 | ||||
| chr2:55616581-55616960 | Common:4; Rare:128 | ||||
| chr2:55616899-55617299 | Common:1; Rare:147 | ||||
| chr2:55617460-55619163 | Common:48; Rare:1863 | ||||
| chr2:55693054-55694030 | Common:6; Rare:764; Clinvar (benign):11 | ||||
| chr2:58046336-58046940 | Common:18; Rare:758 | ||||
| chr2:58046910-58047458 | Common:4; Rare:727 | ||||
| chr2:58240966-58241162 | Rare:65 | ||||
| chr2:58241211-58241710 | Common:7; Rare:692; Clinvar:28; Clinvar (benign):9; Clinvar (pathogenic):2 | ||||
| chr2:60756000-60756400 | Common:2; Rare:368 | ||||
| chr2:60756465-60756940 | Common:2; Rare:228 | ||||
| chr2:60881022-60881229 | Rare:101 | ||||
| chr2:60881173-60881752 | Common:12; Rare:650 | ||||
| chr2:60881873-60882282 | Common:2; Rare:215 | ||||
| chr2:61016637-61018021 | Common:33; Rare:1254; Clinvar:16; Clinvar (benign):2 |