| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:3797264-3797354 | Common:2; Rare:27 | ||||
| chr11:3797422-3798161 | Common:1; Rare:265 | ||||
| chr11:3798308-3798381 | Rare:19 | ||||
| chr11:3807947-3808224 | Common:4; Rare:49 | ||||
| chr11:3808514-3808658 | Common:2; Rare:48 | ||||
| chr11:3840657-3841279 | Common:3; Rare:183 | ||||
| chr11:3841296-3841869 | Common:2; Rare:128 | ||||
| chr11:3855013-3855228 | Common:3; Rare:56 | ||||
| chr11:3855438-3855800 | Common:2; Rare:73 | ||||
| chr11:3855882-3856065 | Common:1; Rare:35 | ||||
| chr11:3856289-3856502 | Rare:53; Clinvar (benign):2 | ||||
| chr11:4094254-4094427 | Common:3; Rare:33 | ||||
| chr11:4094529-4094911 | Common:2; Rare:105 | ||||
| chr11:4095122-4095300 | Rare:49 | ||||
| chr11:4393625-4393814 | Common:1; Rare:46 |