| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65502887-65503536 | Common:3; Rare:289 | ||||
| chr11:65503663-65503708 | Rare:20 | ||||
| chr11:65503999-65504247 | Common:1; Rare:118 | ||||
| chr11:65524821-65525126 | Rare:45 | ||||
| chr11:65570297-65570510 | Rare:81 | ||||
| chr11:65575844-65576071 | Common:3; Rare:65 | ||||
| chr11:65614206-65614415 | Rare:44 | ||||
| chr11:65638002-65638147 | Common:3; Rare:66 | ||||
| chr11:65662884-65663012 | Common:1; Rare:35 | ||||
| chr11:65712221-65712270 | Rare:18 | ||||
| chr11:65856996-65857319 | Common:4; Rare:98 | ||||
| chr11:65860286-65860472 | Common:1; Rare:65 | ||||
| chr11:65888462-65888750 | Common:1; Rare:82 | ||||
| chr11:65919389-65919736 | Rare:113 | ||||
| chr11:66002105-66002520 | Common:3; Rare:115; Clinvar:6; Clinvar (benign):3 |