| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:17543656-17543825 | Common:2; Rare:41 | ||||
| chr11:17544329-17544607 | Common:4; Rare:64; Clinvar:2 | ||||
| chr11:18012396-18012516 | Common:1; Rare:23 | ||||
| chr11:18012866-18013286 | Common:6; Rare:144 | ||||
| chr11:18106019-18106311 | Common:2; Rare:94 | ||||
| chr11:18322035-18322363 | Common:7; Rare:116; Clinvar:2; Clinvar (benign):3 | ||||
| chr11:18322378-18322649 | Common:2; Rare:93 | ||||
| chr11:18323074-18323134 | Common:1; Rare:11 | ||||
| chr11:18393748-18394119 | Common:1; Rare:72 | ||||
| chr11:18394126-18394221 | Common:1; Rare:8 | ||||
| chr11:18394268-18394512 | Common:1; Rare:89; Clinvar (benign):1 | ||||
| chr11:18394526-18394698 | Rare:60 | ||||
| chr11:18394748-18394838 | Common:2; Rare:21 | ||||
| chr11:18396008-18396384 | Common:3; Rare:120 | ||||
| chr11:18455740-18455856 | Rare:32 |