| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:57324890-57325169 | Common:1; Rare:86 | ||||
| chr11:57335733-57335956 | Common:4; Rare:50 | ||||
| chr11:57427070-57427236 | Common:1; Rare:51 | ||||
| chr11:57514899-57515020 | Common:1; Rare:31 | ||||
| chr11:57530682-57530843 | Common:1; Rare:41 | ||||
| chr11:57597613-57597720 | Rare:27; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:57657522-57657773 | Common:4; Rare:63 | ||||
| chr11:57712175-57712651 | Common:9; Rare:163 | ||||
| chr11:58578100-58578532 | Common:4; Rare:138 | ||||
| chr11:59142721-59142951 | Common:1; Rare:42 | ||||
| chr11:59668991-59669334 | Rare:118 | ||||
| chr11:59810726-59810827 | Common:2; Rare:27 | ||||
| chr11:60699211-60699546 | Common:1; Rare:51 | ||||
| chr11:60906514-60906787 | Rare:68 | ||||
| chr11:60913989-60914240 | Common:1; Rare:60 |