| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:118997980-118998152 | Common:4; Rare:46 | ||||
| chr11:119018659-119018789 | Common:4; Rare:59 | ||||
| chr11:119067630-119067816 | Common:3; Rare:62 | ||||
| chr11:119095394-119095676 | Common:2; Rare:113 | ||||
| chr11:119121273-119121616 | Common:1; Rare:78 | ||||
| chr11:119206180-119206367 | Common:5; Rare:84; Clinvar:7; Clinvar (benign):4 | ||||
| chr11:119334282-119334536 | Rare:67 | ||||
| chr11:121292569-121292798 | Rare:80; Clinvar:3 | ||||
| chr11:123062440-123062662 | Common:2; Rare:101 | ||||
| chr11:123480510-123480574 | Rare:14 | ||||
| chr11:124673747-124673929 | Common:4; Rare:47 | ||||
| chr11:124954015-124954202 | Common:4; Rare:50 | ||||
| chr11:125592588-125592904 | Common:6; Rare:102 | ||||
| chr11:125625871-125625993 | Rare:40 | ||||
| chr11:125887480-125887727 | Common:2; Rare:78 |