| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:16607725-16607953 | Common:1; Rare:30 | ||||
| chr11:16612962-16613167 | Common:1; Rare:36 | ||||
| chr11:16738432-16738854 | Common:3; Rare:103 | ||||
| chr11:16881545-16881571 | Common:1; Rare:3 | ||||
| chr11:17077587-17077944 | Common:2; Rare:149 | ||||
| chr11:17207919-17208098 | Common:1; Rare:68 | ||||
| chr11:17276546-17276823 | Common:5; Rare:78; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr11:17276919-17277052 | Rare:25 | ||||
| chr11:17351706-17352011 | Common:2; Rare:59 | ||||
| chr11:18012875-18013264 | Common:6; Rare:132 | ||||
| chr11:18105949-18106308 | Common:4; Rare:122 | ||||
| chr11:18295421-18295597 | Rare:22 | ||||
| chr11:18321627-18321668 | Common:1; Rare:7 | ||||
| chr11:18322049-18322379 | Common:6; Rare:119; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:18322389-18322675 | Common:2; Rare:94 |