| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:241701290-241701640 | Common:8; Rare:158 | ||||
| chr2:241701841-241702062 | Common:2; Rare:173 | ||||
| chr2:241734427-241734883 | Common:15; Rare:259; Clinvar:5; Clinvar (benign):1 | ||||
| chr2:241735410-241735800 | Common:5; Rare:218; Clinvar:5; Clinvar (benign):4 | ||||
| chr20:297385-297621 | Common:4; Rare:70 | ||||
| chr20:325250-325615 | Rare:214 | ||||
| chr20:325762-325938 | Rare:87 | ||||
| chr20:347640-347950 | Common:4; Rare:150 | ||||
| chr20:348090-348400 | Common:3; Rare:98 | ||||
| chr20:380668-381424 | Common:19; Rare:364 | ||||
| chr20:406960-407420 | Common:4; Rare:96 | ||||
| chr20:407856-408130 | Common:47; Rare:122 | ||||
| chr20:408233-408496 | Common:2; Rare:110 | ||||
| chr20:462457-462573 | Common:1; Rare:63 | ||||
| chr20:543631-543877 | Rare:149 |