| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:1309490-1309897 | Common:14; Rare:748 | ||||
| chr11:1389490-1390020 | Common:5; Rare:196 | ||||
| chr11:1572160-1572520 | Common:9; Rare:398 | ||||
| chr11:1762352-1762974 | Common:9; Rare:216 | ||||
| chr11:1763814-1764214 | Common:16; Rare:570; Clinvar:21; Clinvar (benign):20 | ||||
| chr11:1947104-1947504 | Common:5; Rare:93 | ||||
| chr11:2270920-2271240 | Common:4; Rare:82 | ||||
| chr11:2301605-2302370 | Common:18; Rare:549 | ||||
| chr11:2303535-2303935 | Common:5; Rare:77 | ||||
| chr11:2377309-2378005 | Common:23; Rare:525; Clinvar:3 | ||||
| chr11:2399599-2399999 | Common:9; Rare:98 | ||||
| chr11:2400171-2401342 | Common:44; Rare:1107 | ||||
| chr11:2401338-2401607 | Common:7; Rare:60 | ||||
| chr11:2884941-2885599 | Common:5; Rare:215; Clinvar:34; Clinvar (benign):28 | ||||
| chr11:2885725-2886239 | Rare:303; Clinvar:1 |