| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:118911704-118911888 | Common:3; Rare:26 | ||||
| chr11:118925854-118926144 | Common:3; Rare:83 | ||||
| chr11:118956086-118956319 | Common:1; Rare:50 | ||||
| chr11:118997882-118998244 | Common:4; Rare:123 | ||||
| chr11:118998463-118998751 | Common:2; Rare:83 | ||||
| chr11:118999007-118999196 | Common:1; Rare:47 | ||||
| chr11:119018233-119018617 | Common:8; Rare:140 | ||||
| chr11:119018621-119018870 | Common:5; Rare:95 | ||||
| chr11:119029410-119029644 | Common:1; Rare:60; Clinvar:4; Clinvar (benign):1 | ||||
| chr11:119030370-119030520 | Common:1; Rare:36; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:119030756-119030993 | Common:3; Rare:71; Clinvar (benign):3 | ||||
| chr11:119056469-119056744 | Common:2; Rare:83 | ||||
| chr11:119057008-119057323 | Common:1; Rare:109 | ||||
| chr11:119057349-119057720 | Common:4; Rare:104 | ||||
| chr11:119067602-119067876 | Common:4; Rare:86 |