| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:111446673-111446815 | Common:1; Rare:21 | ||||
| chr11:112042265-112042801 | Common:6; Rare:105 | ||||
| chr11:112120313-112120626 | Rare:54 | ||||
| chr11:112157504-112157656 | Rare:24 | ||||
| chr11:112270470-112270830 | Common:7; Rare:70 | ||||
| chr11:112290099-112290275 | Common:1; Rare:34 | ||||
| chr11:112612245-112613126 | Common:9; Rare:241 | ||||
| chr11:112613694-112613808 | Common:3; Rare:18 | ||||
| chr11:113690791-113690935 | Rare:50; Clinvar (benign):2 | ||||
| chr11:116562990-116563390 | Common:4; Rare:84 | ||||
| chr11:116658160-116658530 | Common:4; Rare:66 | ||||
| chr11:116793673-116794201 | Common:4; Rare:166 | ||||
| chr11:116835975-116836122 | Rare:56; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):5 | ||||
| chr11:117221625-117222339 | Common:12; Rare:167 | ||||
| chr11:117809303-117809435 | Rare:19 |