| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:119149090-119149340 | Common:1; Rare:41 | ||||
| chr11:119166367-119166767 | Common:3; Rare:80 | ||||
| chr11:119168083-119168188 | Rare:20 | ||||
| chr11:119168630-119168769 | Rare:28 | ||||
| chr11:119169001-119169345 | Rare:72 | ||||
| chr11:119169378-119169667 | Rare:45 | ||||
| chr11:119195786-119196019 | Rare:48 | ||||
| chr11:119205805-119206101 | Common:2; Rare:88 | ||||
| chr11:119206156-119206378 | Common:5; Rare:97; Clinvar:8; Clinvar (benign):4 | ||||
| chr11:119315720-119316843 | Common:4; Rare:272 | ||||
| chr11:119317094-119317316 | Rare:69 | ||||
| chr11:119334249-119334570 | Rare:91 | ||||
| chr11:119364172-119364311 | Common:2; Rare:58 | ||||
| chr11:119381602-119381824 | Common:1; Rare:48 | ||||
| chr11:119729139-119729365 | Common:1; Rare:61 |