| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:118572296-118572457 | Common:3; Rare:56 | ||||
| chr11:118790904-118791259 | Rare:101 | ||||
| chr11:118997956-118998193 | Common:4; Rare:80 | ||||
| chr11:119018280-119018452 | Common:6; Rare:71 | ||||
| chr11:119018454-119018539 | Common:2; Rare:38 | ||||
| chr11:119018620-119018798 | Common:5; Rare:74 | ||||
| chr11:119057042-119057481 | Common:3; Rare:165 | ||||
| chr11:119067632-119067824 | Common:3; Rare:64 | ||||
| chr11:119084795-119084939 | Common:1; Rare:43; Clinvar (benign):1 | ||||
| chr11:119095426-119095777 | Common:3; Rare:110 | ||||
| chr11:119121260-119121626 | Common:1; Rare:91 | ||||
| chr11:119206180-119206409 | Common:5; Rare:101; Clinvar:8; Clinvar (benign):4 | ||||
| chr11:119317110-119317284 | Rare:60 | ||||
| chr11:119334264-119334561 | Rare:79 | ||||
| chr11:119381607-119381843 | Common:1; Rare:51 |