| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:112086729-112086941 | Rare:89; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):4 | ||||
| chr11:112164068-112164364 | Common:1; Rare:52 | ||||
| chr11:112226300-112226446 | Rare:66 | ||||
| chr11:112961307-112961654 | Common:4; Rare:170 | ||||
| chr11:113314408-113314615 | Rare:74 | ||||
| chr11:113875491-113875775 | Common:4; Rare:103 | ||||
| chr11:114059385-114059789 | Rare:86 | ||||
| chr11:114059808-114059933 | Common:1; Rare:23 | ||||
| chr11:114296237-114296602 | Rare:70 | ||||
| chr11:114400400-114400753 | Common:2; Rare:135 | ||||
| chr11:114439643-114439672 | Rare:5 | ||||
| chr11:116772965-116773280 | Common:1; Rare:95 | ||||
| chr11:116787979-116788104 | Rare:35 | ||||
| chr11:117144101-117144418 | Common:6; Rare:132 | ||||
| chr11:117198994-117199524 | Common:6; Rare:143 |