| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:47565540-47565620 | Common:2; Rare:13 | ||||
| chr11:47578952-47579136 | Rare:98; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:47642466-47642713 | Rare:101 | ||||
| chr11:47848300-47848398 | Common:1; Rare:51 | ||||
| chr11:57324883-57325183 | Common:1; Rare:100 | ||||
| chr11:57712018-57712653 | Common:10; Rare:215 | ||||
| chr11:58578101-58578240 | Common:1; Rare:35 | ||||
| chr11:58578827-58579192 | Common:5; Rare:109 | ||||
| chr11:59142700-59142939 | Common:1; Rare:41 | ||||
| chr11:59668980-59669293 | Rare:113 | ||||
| chr11:59810733-59810980 | Common:4; Rare:83 | ||||
| chr11:60906431-60906787 | Rare:86 | ||||
| chr11:61333038-61333266 | Rare:80 | ||||
| chr11:61361870-61362023 | Common:1; Rare:35 | ||||
| chr11:61362246-61362417 | Common:2; Rare:50; Clinvar:8; Clinvar (benign):1 |