| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:57763794-57763906 | Rare:15 | ||||
| chr11:58578090-58578508 | Common:4; Rare:133 | ||||
| chr11:58578925-58579192 | Common:3; Rare:71 | ||||
| chr11:59142694-59142922 | Common:1; Rare:38 | ||||
| chr11:59668986-59669316 | Rare:115 | ||||
| chr11:60182516-60182652 | Common:1; Rare:29 | ||||
| chr11:60183943-60184050 | Common:1; Rare:23 | ||||
| chr11:60906399-60906785 | Rare:101 | ||||
| chr11:60924366-60924568 | Common:2; Rare:64 | ||||
| chr11:61161402-61161768 | Common:1; Rare:106 | ||||
| chr11:61333038-61333275 | Common:1; Rare:88 | ||||
| chr11:61361835-61362039 | Common:1; Rare:49 | ||||
| chr11:61362182-61362410 | Common:2; Rare:71; Clinvar:8; Clinvar (benign):1 | ||||
| chr11:61392338-61392649 | Common:2; Rare:73; Clinvar:5; Clinvar (benign):2 | ||||
| chr11:61429263-61429474 | Common:3; Rare:70 |