| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65386404-65386674 | Common:1; Rare:79 | ||||
| chr11:65570422-65570494 | Rare:33 | ||||
| chr11:65614216-65614420 | Rare:41 | ||||
| chr11:65662835-65663030 | Common:1; Rare:52 | ||||
| chr11:65712224-65712270 | Rare:17 | ||||
| chr11:65888442-65888692 | Common:1; Rare:80 | ||||
| chr11:65900381-65900534 | Common:1; Rare:29 | ||||
| chr11:66002128-66002528 | Common:3; Rare:108; Clinvar:3; Clinvar (benign):3 | ||||
| chr11:66347622-66347834 | Common:5; Rare:52 | ||||
| chr11:66480226-66480446 | Common:1; Rare:59 | ||||
| chr11:66638379-66638723 | Common:3; Rare:153 | ||||
| chr11:66958356-66958675 | Common:4; Rare:98; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:67056770-67056882 | Common:1; Rare:32 | ||||
| chr11:67353499-67353830 | Common:2; Rare:87 | ||||
| chr11:67401789-67402075 | Common:3; Rare:103 |