| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:119067624-119067816 | Common:3; Rare:62 | ||||
| chr11:119084808-119084939 | Rare:42 | ||||
| chr11:119095387-119095787 | Common:3; Rare:134 | ||||
| chr11:119101380-119101493 | Rare:31; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr11:119101788-119102189 | Rare:101; Clinvar:4 | ||||
| chr11:119121297-119121626 | Common:1; Rare:72 | ||||
| chr11:119206191-119206367 | Common:5; Rare:78; Clinvar:7; Clinvar (benign):4 | ||||
| chr11:119317110-119317311 | Rare:67 | ||||
| chr11:119334282-119334555 | Rare:73 | ||||
| chr11:119381632-119381843 | Common:1; Rare:43 | ||||
| chr11:121292615-121292793 | Rare:57; Clinvar:3 | ||||
| chr11:122655575-122655901 | Common:3; Rare:77 | ||||
| chr11:123062040-123062345 | Common:5; Rare:134 | ||||
| chr11:123062376-123062677 | Common:4; Rare:141 | ||||
| chr11:123454351-123454676 | Common:2; Rare:56 |