| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:40688077-40688369 | Rare:70; Clinvar (benign):1 | ||||
| chr20:41103830-41104145 | Rare:59 | ||||
| chr20:41174392-41174501 | Common:2; Rare:33 | ||||
| chr20:47357790-47357865 | Rare:14 | ||||
| chr20:49118371-49118513 | Common:2; Rare:36 | ||||
| chr20:50267326-50267566 | Common:4; Rare:45 | ||||
| chr20:50276209-50276343 | Rare:30 | ||||
| chr20:50379318-50379540 | Rare:55 | ||||
| chr20:53592763-53592789 | Rare:7 | ||||
| chr20:62306480-62306725 | Common:2; Rare:86 | ||||
| chr20:62623843-62624180 | Common:1; Rare:69 | ||||
| chr20:62651990-62652287 | Rare:59 | ||||
| chr21:16588521-16588712 | Common:1; Rare:50 | ||||
| chr21:26964476-26964756 | Common:1; Rare:53 | ||||
| chr21:26965492-26965606 | Common:1; Rare:49 |