| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:85854721-85854740 | Rare:4 | ||||
| chr11:85854832-85855156 | Common:5; Rare:94 | ||||
| chr11:86068267-86068759 | Rare:155 | ||||
| chr11:86068929-86069523 | Common:3; Rare:191 | ||||
| chr11:86069529-86070001 | Common:2; Rare:113 | ||||
| chr11:86070057-86070096 | Rare:7 | ||||
| chr11:86244372-86244892 | Common:2; Rare:144 | ||||
| chr11:86244903-86245515 | Common:2; Rare:228 | ||||
| chr11:86302062-86302337 | Common:2; Rare:49 | ||||
| chr11:86302367-86302535 | Rare:47 | ||||
| chr11:86302641-86302712 | Rare:10 | ||||
| chr11:86672136-86672189 | Rare:6 | ||||
| chr11:86800274-86800608 | Common:2; Rare:119 | ||||
| chr11:86955185-86955271 | Rare:18; Clinvar:1 | ||||
| chr11:86955325-86955689 | Common:1; Rare:125; Clinvar:2; Clinvar (benign):1 |