| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:63865092-63865358 | Common:2; Rare:103 | ||||
| chr20:63956380-63956653 | Common:1; Rare:104 | ||||
| chr20:63969837-63970095 | Common:3; Rare:89 | ||||
| chr20:63981014-63981278 | Common:4; Rare:76; Clinvar:7; Clinvar (benign):4 | ||||
| chr20:64062993-64063270 | Common:1; Rare:101 | ||||
| chr20:64164114-64164471 | Common:1; Rare:61 | ||||
| chr21:14383111-14383510 | Common:3; Rare:113 | ||||
| chr21:17819324-17819455 | Common:1; Rare:46 | ||||
| chr21:20998201-20998455 | Rare:139 | ||||
| chr21:25607473-25607622 | Rare:70 | ||||
| chr21:25639095-25639405 | Common:3; Rare:65 | ||||
| chr21:25639600-25639816 | Common:1; Rare:47 | ||||
| chr21:25734851-25735506 | Common:5; Rare:223 | ||||
| chr21:25735517-25735902 | Common:4; Rare:100 | ||||
| chr21:26170565-26170928 | Common:6; Rare:117; Clinvar:5; Clinvar (benign):2 |