| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:119018626-119018795 | Common:5; Rare:71 | ||||
| chr11:119057042-119057481 | Common:3; Rare:165 | ||||
| chr11:119067630-119067837 | Common:3; Rare:70 | ||||
| chr11:119084795-119084915 | Common:1; Rare:33; Clinvar (benign):1 | ||||
| chr11:119095408-119095481 | Common:1; Rare:48 | ||||
| chr11:119121284-119121626 | Common:1; Rare:77 | ||||
| chr11:119206175-119206396 | Common:5; Rare:99; Clinvar:8; Clinvar (benign):4 | ||||
| chr11:119317124-119317284 | Rare:53 | ||||
| chr11:119334283-119334561 | Rare:75 | ||||
| chr11:119364145-119364402 | Common:2; Rare:111 | ||||
| chr11:119379049-119379145 | Rare:15 | ||||
| chr11:120336312-120336441 | Rare:59 | ||||
| chr11:120336879-120336938 | Rare:10 | ||||
| chr11:121292563-121292927 | Rare:111; Clinvar:3 | ||||
| chr11:123062064-123062345 | Common:5; Rare:119 |