| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:93784836-93785130 | Common:1; Rare:61 | ||||
| chr11:94128754-94129204 | Common:4; Rare:154 | ||||
| chr11:94493789-94494053 | Common:4; Rare:77; Clinvar (benign):1 | ||||
| chr11:94543811-94543884 | Common:2; Rare:17 | ||||
| chr11:94768059-94768405 | Common:2; Rare:89 | ||||
| chr11:94973531-94973719 | Rare:56 | ||||
| chr11:95066826-95066919 | Rare:18 | ||||
| chr11:95067446-95067573 | Rare:46 | ||||
| chr11:95089735-95089907 | Common:3; Rare:75 | ||||
| chr11:95789478-95789872 | Common:4; Rare:182 | ||||
| chr11:95790338-95790690 | Common:3; Rare:138 | ||||
| chr11:95924055-95924164 | Rare:45 | ||||
| chr11:96389846-96390050 | Common:1; Rare:87 | ||||
| chr11:99020839-99021052 | Rare:60 | ||||
| chr11:101914848-101915330 | Common:8; Rare:141 |