| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:118634840-118635029 | Common:5; Rare:56 | ||||
| chr11:118790855-118791321 | Common:1; Rare:155 | ||||
| chr11:118997973-118998193 | Common:4; Rare:71 | ||||
| chr11:119018280-119018538 | Common:8; Rare:110 | ||||
| chr11:119018620-119018806 | Common:5; Rare:75 | ||||
| chr11:119057033-119057481 | Common:3; Rare:167 | ||||
| chr11:119067602-119067874 | Common:4; Rare:84 | ||||
| chr11:119084795-119084956 | Common:1; Rare:47; Clinvar (benign):1 | ||||
| chr11:119101788-119102187 | Rare:101; Clinvar:4 | ||||
| chr11:119121297-119121626 | Common:1; Rare:72 | ||||
| chr11:119206174-119206383 | Common:5; Rare:96; Clinvar:8; Clinvar (benign):4 | ||||
| chr11:119317106-119317275 | Rare:57 | ||||
| chr11:119379018-119379246 | Rare:45 | ||||
| chr11:119381597-119381839 | Common:1; Rare:56 | ||||
| chr11:120210743-120210781 | Common:1; Rare:5 |