| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:59668986-59669328 | Rare:119 | ||||
| chr11:60183745-60184050 | Common:1; Rare:67 | ||||
| chr11:60906421-60906737 | Rare:79 | ||||
| chr11:60914139-60914252 | Rare:31 | ||||
| chr11:60952099-60952456 | Common:1; Rare:71 | ||||
| chr11:61161402-61161748 | Common:1; Rare:99 | ||||
| chr11:61333038-61333275 | Common:1; Rare:88 | ||||
| chr11:61361842-61362049 | Common:2; Rare:48; Clinvar:2 | ||||
| chr11:61362255-61362404 | Common:1; Rare:42; Clinvar:7 | ||||
| chr11:61392527-61392651 | Common:2; Rare:41; Clinvar:3; Clinvar (benign):2 | ||||
| chr11:61429892-61430164 | Common:1; Rare:120; Clinvar:3; Clinvar (benign):5 | ||||
| chr11:61792573-61792944 | Common:5; Rare:97 | ||||
| chr11:61816781-61817059 | Rare:72 | ||||
| chr11:61917361-61917653 | Common:2; Rare:99 | ||||
| chr11:61967285-61967690 | Common:2; Rare:155; Clinvar:4 |