| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:16738961-16739001 | Rare:10 | ||||
| chr11:17014386-17014530 | Common:1; Rare:76 | ||||
| chr11:17077253-17077454 | Rare:50 | ||||
| chr11:17077568-17078143 | Common:5; Rare:215 | ||||
| chr11:17078147-17078328 | Rare:52 | ||||
| chr11:17207876-17208179 | Common:2; Rare:114 | ||||
| chr11:17208295-17208497 | Rare:40 | ||||
| chr11:17276247-17276317 | Rare:19 | ||||
| chr11:17276423-17276766 | Common:3; Rare:96; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr11:17351581-17351821 | Common:1; Rare:53 | ||||
| chr11:17351873-17352037 | Common:2; Rare:39 | ||||
| chr11:17352236-17352298 | Rare:11 | ||||
| chr11:17389308-17389487 | Common:2; Rare:35 | ||||
| chr11:18012871-18013248 | Common:6; Rare:129 | ||||
| chr11:18105992-18106314 | Common:3; Rare:110 |