| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:118264284-118264591 | Common:1; Rare:50 | ||||
| chr11:118344307-118344365 | Rare:11 | ||||
| chr11:118359415-118359673 | Common:3; Rare:105 | ||||
| chr11:118572724-118572893 | Common:2; Rare:31 | ||||
| chr11:118790904-118791290 | Rare:122 | ||||
| chr11:118997980-118998193 | Common:4; Rare:66 | ||||
| chr11:119018280-119018813 | Common:13; Rare:205 | ||||
| chr11:119055243-119055566 | Rare:94 | ||||
| chr11:119057028-119057455 | Common:3; Rare:159 | ||||
| chr11:119067624-119067825 | Common:3; Rare:65 | ||||
| chr11:119101750-119101913 | Rare:42; Clinvar:1 | ||||
| chr11:119110624-119110891 | Rare:74 | ||||
| chr11:119121307-119121626 | Common:1; Rare:69 | ||||
| chr11:119206178-119206369 | Common:5; Rare:87; Clinvar:7; Clinvar (benign):4 | ||||
| chr11:119317110-119317412 | Rare:85 |