| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:10091771-10091893 | Common:3; Rare:39 | ||||
| chr2:10092288-10092479 | Common:3; Rare:67 | ||||
| chr2:10105968-10106164 | Rare:23 | ||||
| chr2:10118258-10118425 | Rare:28 | ||||
| chr2:10120105-10120742 | Common:3; Rare:181 | ||||
| chr2:10121377-10121442 | Rare:13 | ||||
| chr2:10331177-10331387 | Common:3; Rare:50 | ||||
| chr2:10378192-10378347 | Common:2; Rare:29 | ||||
| chr2:10382836-10382875 | Rare:6 | ||||
| chr2:10408456-10408630 | Common:1; Rare:33 | ||||
| chr2:10409195-10409326 | Common:2; Rare:22 | ||||
| chr2:10410284-10410639 | Common:1; Rare:53 | ||||
| chr2:10410803-10410955 | Common:1; Rare:20 | ||||
| chr2:10412510-10412643 | Common:1; Rare:21 | ||||
| chr2:10445546-10445669 | Common:2; Rare:22 |