| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:58578121-58578499 | Common:4; Rare:119 | ||||
| chr11:58578855-58579192 | Common:4; Rare:101 | ||||
| chr11:58731853-58732072 | Rare:40 | ||||
| chr11:58732092-58732159 | Rare:14 | ||||
| chr11:59142718-59142951 | Common:1; Rare:42 | ||||
| chr11:59668976-59669312 | Rare:118 | ||||
| chr11:60841918-60842120 | Common:2; Rare:75 | ||||
| chr11:60906522-60906798 | Rare:68 | ||||
| chr11:60913835-60914252 | Common:1; Rare:88 | ||||
| chr11:61161402-61161748 | Common:1; Rare:99 | ||||
| chr11:61332994-61333266 | Rare:94 | ||||
| chr11:61361844-61362039 | Common:1; Rare:45 | ||||
| chr11:61362239-61362410 | Common:2; Rare:51; Clinvar:8; Clinvar (benign):1 | ||||
| chr11:61392527-61392658 | Common:2; Rare:45; Clinvar:3; Clinvar (benign):2 | ||||
| chr11:61429885-61430147 | Common:1; Rare:109; Clinvar (benign):3 |