| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:70422897-70422995 | Rare:35 | ||||
| chr11:71448285-71448699 | Common:4; Rare:112; Clinvar:4; Clinvar (benign):1 | ||||
| chr11:71479178-71479255 | Common:1; Rare:12 | ||||
| chr11:71479820-71480244 | Common:5; Rare:81 | ||||
| chr11:71928776-71929131 | Common:1; Rare:105 | ||||
| chr11:72039787-72039909 | Common:1; Rare:17 | ||||
| chr11:72040734-72040868 | Rare:25 | ||||
| chr11:72041001-72041190 | Common:1; Rare:37 | ||||
| chr11:72041199-72041227 | Rare:1 | ||||
| chr11:72041825-72041996 | Common:2; Rare:34 | ||||
| chr11:72080420-72080861 | Common:2; Rare:106; Clinvar:8 | ||||
| chr11:72112189-72112595 | Rare:103 | ||||
| chr11:72112633-72113107 | Common:6; Rare:179 | ||||
| chr11:72224154-72224270 | Common:2; Rare:24 | ||||
| chr11:72225123-72225162 | Rare:3 |