| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:119206175-119206391 | Common:5; Rare:98; Clinvar:8; Clinvar (benign):4 | ||||
| chr11:119364139-119364390 | Common:2; Rare:109 | ||||
| chr11:119729410-119729564 | Rare:41 | ||||
| chr11:120185488-120185736 | Common:1; Rare:41 | ||||
| chr11:120210745-120210808 | Common:2; Rare:13 | ||||
| chr11:120211646-120211969 | Common:3; Rare:80 | ||||
| chr11:120337079-120337112 | Rare:2 | ||||
| chr11:121292395-121292793 | Rare:107; Clinvar:3 | ||||
| chr11:121451385-121451773 | Common:1; Rare:67 | ||||
| chr11:121452842-121452936 | Rare:18 | ||||
| chr11:123062062-123062307 | Common:5; Rare:103 | ||||
| chr11:123062431-123062677 | Common:3; Rare:111 | ||||
| chr11:123741632-123741977 | Common:1; Rare:91 | ||||
| chr11:124622653-124622946 | Common:6; Rare:92 | ||||
| chr11:124673706-124673940 | Common:4; Rare:72 |