| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:3856124-3857006 | Common:3; Rare:334; Clinvar:2; Clinvar (benign):5 | ||||
| chr11:3866216-3866663 | Common:9; Rare:200 | ||||
| chr11:3867200-3868110 | Common:14; Rare:324 | ||||
| chr11:4058080-4058480 | Common:2; Rare:62 | ||||
| chr11:4094521-4095341 | Common:16; Rare:896 | ||||
| chr11:4393224-4393935 | Common:5; Rare:323 | ||||
| chr11:4607642-4608042 | Common:11; Rare:214 | ||||
| chr11:4608027-4608460 | Common:5; Rare:474 | ||||
| chr11:4881970-4882520 | Common:7; Rare:322 | ||||
| chr11:5131788-5132188 | Common:2; Rare:245 | ||||
| chr11:5151685-5152118 | Common:6; Rare:339 | ||||
| chr11:5234330-5234830 | Common:13; Rare:307; Clinvar:21; Clinvar (pathogenic):4 | ||||
| chr11:5250044-5250795 | Common:29; Rare:463; Clinvar (pathogenic):2 | ||||
| chr11:5252738-5253138 | Common:3; Rare:92 | ||||
| chr11:5254161-5254271 | Common:1; Rare:27 |