| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:241508170-241508450 | Common:2; Rare:128 | ||||
| chr2:241508442-241509011 | Common:10; Rare:460 | ||||
| chr2:241558612-241558820 | Rare:151 | ||||
| chr2:241558880-241559285 | Common:9; Rare:337 | ||||
| chr2:241636942-241637199 | Rare:240 | ||||
| chr2:241637222-241637754 | Common:6; Rare:645 | ||||
| chr2:241686108-241686508 | Common:2; Rare:96 | ||||
| chr2:241686651-241687185 | Common:15; Rare:487 | ||||
| chr2:241701220-241702126 | Common:16; Rare:630 | ||||
| chr2:241702219-241702538 | Common:4; Rare:201 | ||||
| chr2:241734406-241734927 | Common:28; Rare:469; Clinvar:9; Clinvar (benign):3 | ||||
| chr2:241735091-241735840 | Common:13; Rare:447; Clinvar:10; Clinvar (benign):10 | ||||
| chr2:241776748-241776884 | Common:1; Rare:29 | ||||
| chr20:290356-290595 | Common:14; Rare:97 | ||||
| chr20:297233-297671 | Common:14; Rare:289 |