| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:118790199-118790322 | Common:2; Rare:37 | ||||
| chr11:118790460-118790607 | Common:1; Rare:37 | ||||
| chr11:118790654-118790798 | Common:2; Rare:32 | ||||
| chr11:118790873-118791525 | Common:3; Rare:196 | ||||
| chr11:118791569-118791939 | Common:2; Rare:98 | ||||
| chr11:118910452-118910587 | Common:2; Rare:36 | ||||
| chr11:118910620-118910764 | Common:1; Rare:52 | ||||
| chr11:118910829-118910947 | Common:3; Rare:27 | ||||
| chr11:118911107-118911342 | Rare:70 | ||||
| chr11:118925853-118925997 | Common:1; Rare:42 | ||||
| chr11:118997897-118998203 | Common:4; Rare:100 | ||||
| chr11:119018222-119018599 | Common:8; Rare:139 | ||||
| chr11:119018605-119018880 | Common:5; Rare:104 | ||||
| chr11:119030342-119030404 | Rare:15 | ||||
| chr11:119030408-119030514 | Common:1; Rare:24; Clinvar:1; Clinvar (benign):1 |