| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:118572476-118572528 | Rare:21 | ||||
| chr11:118790864-118791266 | Rare:117 | ||||
| chr11:118910540-118910686 | Common:1; Rare:53 | ||||
| chr11:118925912-118926162 | Common:2; Rare:72 | ||||
| chr11:118997958-118998189 | Common:4; Rare:76 | ||||
| chr11:119017911-119018801 | Common:16; Rare:329 | ||||
| chr11:119018967-119019309 | Common:4; Rare:139 | ||||
| chr11:119057070-119057442 | Common:3; Rare:145 | ||||
| chr11:119067639-119067824 | Common:3; Rare:63 | ||||
| chr11:119101372-119101602 | Rare:67; Clinvar:3; Clinvar (pathogenic):2 | ||||
| chr11:119121269-119121636 | Common:1; Rare:88 | ||||
| chr11:119206175-119206339 | Common:5; Rare:77; Clinvar:6; Clinvar (benign):4 | ||||
| chr11:119381602-119381836 | Common:1; Rare:51 | ||||
| chr11:120210893-120211032 | Rare:36 | ||||
| chr11:122655513-122655791 | Common:1; Rare:64 |