| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:47409174-47409247 | Rare:13 | ||||
| chr11:47426172-47426767 | Common:1; Rare:153 | ||||
| chr11:47426861-47426979 | Common:1; Rare:23 | ||||
| chr11:47495006-47495153 | Rare:24 | ||||
| chr11:47552646-47552790 | Common:1; Rare:62 | ||||
| chr11:47553016-47553469 | Common:4; Rare:134 | ||||
| chr11:47565355-47565801 | Common:4; Rare:96 | ||||
| chr11:47565819-47565901 | Common:1; Rare:36 | ||||
| chr11:47578571-47578784 | Rare:55 | ||||
| chr11:47578891-47579161 | Rare:132; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:47579223-47579317 | Rare:38; Clinvar (benign):3 | ||||
| chr11:47642063-47642199 | Rare:39 | ||||
| chr11:47642212-47642252 | Rare:8 | ||||
| chr11:47642274-47642350 | Common:1; Rare:22 | ||||
| chr11:47642431-47642895 | Rare:150 |