| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:119205838-119206038 | Common:2; Rare:61 | ||||
| chr11:119206180-119206396 | Common:5; Rare:96; Clinvar:8; Clinvar (benign):4 | ||||
| chr11:119311413-119311564 | Rare:54 | ||||
| chr11:119317106-119317275 | Rare:57 | ||||
| chr11:119381602-119381863 | Common:1; Rare:60 | ||||
| chr11:120128829-120129028 | Rare:43 | ||||
| chr11:120336145-120336579 | Rare:168 | ||||
| chr11:121292569-121292798 | Rare:80; Clinvar:3 | ||||
| chr11:121452084-121452332 | Common:1; Rare:68 | ||||
| chr11:122882854-122882956 | Rare:28 | ||||
| chr11:123062062-123062339 | Common:5; Rare:120 | ||||
| chr11:123062398-123062672 | Common:4; Rare:125 | ||||
| chr11:123741612-123741707 | Common:1; Rare:29 | ||||
| chr11:124673682-124673949 | Common:5; Rare:84 | ||||
| chr11:124751729-124751732 | Common:1 |