| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:75399398-75399577 | Common:3; Rare:77 | ||||
| chr11:75561935-75562259 | Rare:69; Clinvar:4; Clinvar (benign):1 | ||||
| chr11:75562738-75562846 | Common:1; Rare:23 | ||||
| chr11:75814746-75814846 | Rare:20 | ||||
| chr11:76380908-76380995 | Rare:30 | ||||
| chr11:76381123-76381408 | Common:4; Rare:98 | ||||
| chr11:76444619-76445091 | Common:1; Rare:114 | ||||
| chr11:76783054-76783366 | Common:9; Rare:103 | ||||
| chr11:76860669-76860962 | Common:4; Rare:92 | ||||
| chr11:77411912-77412127 | Common:3; Rare:55 | ||||
| chr11:77637588-77637901 | Common:1; Rare:94 | ||||
| chr11:77820941-77821209 | Common:1; Rare:83 | ||||
| chr11:77994645-77995020 | Common:1; Rare:113 | ||||
| chr11:78079701-78079943 | Common:2; Rare:73 | ||||
| chr11:78139574-78139815 | Common:3; Rare:93; Clinvar:2 |