| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:63707855-63708095 | Rare:66 | ||||
| chr20:63864980-63865351 | Common:2; Rare:131 | ||||
| chr20:63946261-63946457 | Common:1; Rare:96 | ||||
| chr20:63956368-63956424 | Common:1; Rare:30 | ||||
| chr21:17819327-17819488 | Common:1; Rare:57 | ||||
| chr21:25607473-25607545 | Rare:41 | ||||
| chr21:25734851-25735479 | Common:5; Rare:217 | ||||
| chr21:25735640-25735931 | Common:4; Rare:76 | ||||
| chr21:26170581-26170926 | Common:5; Rare:110; Clinvar:5; Clinvar (benign):2 | ||||
| chr21:26843067-26843158 | Common:3; Rare:14 | ||||
| chr21:26845248-26845673 | Common:2; Rare:116 | ||||
| chr21:29019319-29019428 | Common:5; Rare:41 | ||||
| chr21:29024512-29024737 | Common:3; Rare:94 | ||||
| chr21:29024876-29024979 | Rare:19 | ||||
| chr21:29073538-29073865 | Common:2; Rare:102 |