| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:111913145-111913269 | Rare:38 | ||||
| chr11:112073985-112074349 | Common:1; Rare:77 | ||||
| chr11:112086710-112086910 | Rare:84; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr11:112226265-112226443 | Rare:75 | ||||
| chr11:113314403-113314598 | Rare:69 | ||||
| chr11:113875493-113875771 | Common:4; Rare:101 | ||||
| chr11:114296237-114296572 | Rare:63 | ||||
| chr11:114400456-114400755 | Common:2; Rare:118 | ||||
| chr11:116772963-116773066 | Rare:36 | ||||
| chr11:117144232-117144350 | Common:1; Rare:59 | ||||
| chr11:117199008-117199320 | Common:6; Rare:100 | ||||
| chr11:117232526-117232726 | Common:2; Rare:68 | ||||
| chr11:118359421-118359650 | Common:3; Rare:100 | ||||
| chr11:118790904-118791255 | Rare:100 | ||||
| chr11:118910501-118910712 | Common:2; Rare:74 |