| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:118634697-118635044 | Common:5; Rare:96 | ||||
| chr11:118790875-118791308 | Rare:146 | ||||
| chr11:118925395-118925488 | Rare:20 | ||||
| chr11:118997973-118998317 | Common:4; Rare:116 | ||||
| chr11:119018280-119018452 | Common:6; Rare:71 | ||||
| chr11:119018454-119018845 | Common:7; Rare:143 | ||||
| chr11:119057034-119057481 | Common:3; Rare:166 | ||||
| chr11:119067624-119067843 | Common:3; Rare:71 | ||||
| chr11:119110622-119110947 | Rare:83 | ||||
| chr11:119121274-119121635 | Common:1; Rare:86 | ||||
| chr11:119168441-119168770 | Common:3; Rare:63; Clinvar:1 | ||||
| chr11:119205861-119206073 | Common:2; Rare:73 | ||||
| chr11:119206178-119206432 | Common:5; Rare:111; Clinvar:8; Clinvar (benign):6 | ||||
| chr11:119311849-119312145 | Common:1; Rare:97 | ||||
| chr11:119317097-119317275 | Rare:59 |