| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:58578813-58579192 | Common:5; Rare:115 | ||||
| chr11:59142683-59142951 | Common:1; Rare:49 | ||||
| chr11:59212807-59213022 | Rare:61 | ||||
| chr11:59615766-59615984 | Rare:56 | ||||
| chr11:59668975-59669334 | Rare:127 | ||||
| chr11:59810726-59811115 | Common:7; Rare:116 | ||||
| chr11:60841833-60842141 | Common:2; Rare:98 | ||||
| chr11:60906426-60906800 | Rare:90 | ||||
| chr11:60913950-60914244 | Common:1; Rare:69 | ||||
| chr11:60952110-60952285 | Common:1; Rare:33 | ||||
| chr11:61161402-61161755 | Common:1; Rare:101 | ||||
| chr11:61333020-61333290 | Common:1; Rare:97 | ||||
| chr11:61333300-61333358 | Rare:24 | ||||
| chr11:61361842-61362055 | Common:2; Rare:49; Clinvar:2 | ||||
| chr11:61362212-61362427 | Common:2; Rare:62; Clinvar:8; Clinvar (benign):1 |