| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:41589719-41589904 | Common:1; Rare:80 | ||||
| chr22:41620998-41621410 | Common:7; Rare:149 | ||||
| chr22:41832840-41833355 | Common:3; Rare:170 | ||||
| chr22:41946486-41946656 | Rare:60 | ||||
| chr22:41946708-41946949 | Common:3; Rare:61 | ||||
| chr22:41947077-41947225 | Common:1; Rare:56 | ||||
| chr22:42070737-42070986 | Common:3; Rare:56 | ||||
| chr22:42079431-42079786 | Common:3; Rare:92 | ||||
| chr22:42090604-42090963 | Common:2; Rare:152; Clinvar (pathogenic):1 | ||||
| chr22:42553726-42553969 | Common:1; Rare:73 | ||||
| chr22:42614800-42615245 | Common:5; Rare:190 | ||||
| chr22:42649296-42649566 | Common:4; Rare:99 | ||||
| chr22:42857161-42857463 | Common:3; Rare:123 | ||||
| chr22:43015025-43015384 | Common:3; Rare:137 | ||||
| chr22:43812264-43812441 | Common:2; Rare:59 |