| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65386519-65386674 | Rare:52 | ||||
| chr11:65524830-65525156 | Rare:58 | ||||
| chr11:65570293-65570504 | Rare:81 | ||||
| chr11:65614199-65614407 | Rare:42 | ||||
| chr11:65637844-65638152 | Common:3; Rare:117 | ||||
| chr11:65662842-65663300 | Common:3; Rare:111 | ||||
| chr11:65663302-65663479 | Common:2; Rare:40 | ||||
| chr11:65711869-65712044 | Rare:54 | ||||
| chr11:65712224-65712288 | Rare:21 | ||||
| chr11:65720454-65720585 | Common:1; Rare:74 | ||||
| chr11:65833744-65833998 | Common:1; Rare:55 | ||||
| chr11:65859440-65859696 | Rare:65 | ||||
| chr11:65860273-65860441 | Common:1; Rare:57 | ||||
| chr11:65872701-65872923 | Common:2; Rare:58; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:65873550-65873808 | Common:3; Rare:82 |