| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:18321982-18322670 | Common:50; Rare:1178; Clinvar:14; Clinvar (benign):17 | ||||
| chr11:18393974-18394778 | Common:11; Rare:692; Clinvar (benign):6 | ||||
| chr11:18395930-18397016 | Common:10; Rare:961; Clinvar:3 | ||||
| chr11:18526408-18526808 | Common:8; Rare:196 | ||||
| chr11:18526792-18527300 | Common:11; Rare:704 | ||||
| chr11:18527248-18528142 | Common:14; Rare:278 | ||||
| chr11:18588578-18589051 | Common:16; Rare:541 | ||||
| chr11:18633931-18634669 | Common:24; Rare:808 | ||||
| chr11:18634660-18635040 | Common:11; Rare:273 | ||||
| chr11:18692515-18693828 | Common:10; Rare:329 | ||||
| chr11:18698351-18698902 | Common:26; Rare:400 | ||||
| chr11:18706263-18706988 | Common:3; Rare:179 | ||||
| chr11:19116832-19117232 | Common:10; Rare:260 | ||||
| chr11:19117436-19117836 | Common:3; Rare:111 | ||||
| chr11:19163660-19163960 | Rare:53 |