| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:118607410-118607657 | Common:1; Rare:41 | ||||
| chr11:118621240-118621516 | Rare:57 | ||||
| chr11:118790862-118791259 | Rare:114 | ||||
| chr11:118791261-118791288 | Rare:17 | ||||
| chr11:118997977-118998199 | Common:4; Rare:69 | ||||
| chr11:119018269-119018514 | Common:7; Rare:100 | ||||
| chr11:119018587-119018795 | Common:5; Rare:80 | ||||
| chr11:119057068-119057446 | Common:3; Rare:147 | ||||
| chr11:119067685-119067823 | Common:1; Rare:56 | ||||
| chr11:119084792-119084949 | Common:1; Rare:45; Clinvar (benign):1 | ||||
| chr11:119101821-119102199 | Rare:93; Clinvar:3 | ||||
| chr11:119206175-119206392 | Common:5; Rare:98; Clinvar:8; Clinvar (benign):4 | ||||
| chr11:119317106-119317303 | Rare:67 | ||||
| chr11:119379005-119379106 | Rare:11 | ||||
| chr11:119379108-119379172 | Rare:22 |