| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:119067715-119067816 | Common:1; Rare:39 | ||||
| chr11:119206180-119206325 | Common:5; Rare:67; Clinvar:6; Clinvar (benign):4 | ||||
| chr11:119317106-119317314 | Rare:67 | ||||
| chr11:120128848-120129045 | Rare:41 | ||||
| chr11:124673753-124673929 | Common:4; Rare:45 | ||||
| chr11:124762271-124762451 | Rare:45 | ||||
| chr11:125164558-125164759 | Rare:37 | ||||
| chr11:125592506-125592888 | Common:6; Rare:124 | ||||
| chr11:125625851-125625959 | Rare:39 | ||||
| chr11:125887434-125887727 | Common:2; Rare:89 | ||||
| chr11:126211651-126211798 | Rare:68 | ||||
| chr11:126268814-126269073 | Common:1; Rare:98; Clinvar:1 | ||||
| chr11:126303959-126304081 | Rare:69 | ||||
| chr11:130448448-130448645 | Rare:47 | ||||
| chr11:134253305-134253586 | Common:2; Rare:91; Clinvar (benign):1 |