| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:116772946-116773088 | Rare:56 | ||||
| chr11:117144232-117144344 | Common:1; Rare:57 | ||||
| chr11:117817468-117817484 | Rare:1 | ||||
| chr11:117824531-117824761 | Common:3; Rare:65; Clinvar (benign):2 | ||||
| chr11:118359443-118359650 | Common:3; Rare:91 | ||||
| chr11:118401331-118401661 | Rare:107 | ||||
| chr11:118790904-118791255 | Rare:100 | ||||
| chr11:118910487-118910705 | Common:3; Rare:77 | ||||
| chr11:118997980-118998186 | Common:4; Rare:61 | ||||
| chr11:119018292-119018452 | Common:6; Rare:65 | ||||
| chr11:119018607-119018795 | Common:5; Rare:74 | ||||
| chr11:119057140-119057439 | Common:3; Rare:120 | ||||
| chr11:119067639-119067816 | Common:3; Rare:60 | ||||
| chr11:119121284-119121621 | Common:1; Rare:75 | ||||
| chr11:119206235-119206367 | Common:4; Rare:59; Clinvar:7; Clinvar (benign):4 |