| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:60913810-60913927 | Rare:22 | ||||
| chr11:60913941-60914006 | Rare:6 | ||||
| chr11:60914015-60914521 | Common:2; Rare:130 | ||||
| chr11:60924362-60924581 | Common:2; Rare:68 | ||||
| chr11:61161137-61161297 | Rare:36 | ||||
| chr11:61161314-61161883 | Common:1; Rare:156 | ||||
| chr11:61294401-61294566 | Rare:29 | ||||
| chr11:61294718-61294973 | Rare:62 | ||||
| chr11:61332870-61332888 | Rare:2 | ||||
| chr11:61332996-61333373 | Common:1; Rare:140 | ||||
| chr11:61333774-61333823 | Rare:9 | ||||
| chr11:61334595-61334742 | Rare:30 | ||||
| chr11:61356105-61356309 | Common:1; Rare:46 | ||||
| chr11:61361770-61362074 | Common:2; Rare:72; Clinvar:2 | ||||
| chr11:61362140-61362457 | Common:2; Rare:95; Clinvar:8; Clinvar (benign):1 |