| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:406639-407650 | Common:62; Rare:1193 | ||||
| chr11:414970-415401 | Common:24; Rare:181 | ||||
| chr11:441850-442250 | Common:3; Rare:155 | ||||
| chr11:447950-448690 | Common:22; Rare:745 | ||||
| chr11:450034-450485 | Common:5; Rare:428 | ||||
| chr11:450646-451296 | Common:7; Rare:190 | ||||
| chr11:503367-503767 | Common:4; Rare:231 | ||||
| chr11:504068-504252 | Rare:91 | ||||
| chr11:504284-505267 | Common:19; Rare:592 | ||||
| chr11:505660-506618 | Common:28; Rare:613 | ||||
| chr11:506680-507083 | Common:20; Rare:679 | ||||
| chr11:507141-507966 | Common:30; Rare:1018 | ||||
| chr11:535069-535853 | Common:37; Rare:763; Clinvar (benign):5 | ||||
| chr11:537270-537570 | Common:25; Rare:428 | ||||
| chr11:559646-560439 | Common:12; Rare:438 |