| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:112583316-112583509 | Common:1; Rare:36 | ||||
| chr11:112621042-112621305 | Common:1; Rare:53 | ||||
| chr11:112627619-112628013 | Common:5; Rare:69 | ||||
| chr11:115221601-115221799 | Rare:38 | ||||
| chr11:115920847-115921050 | Common:1; Rare:36 | ||||
| chr11:115921572-115921813 | Common:2; Rare:43 | ||||
| chr11:115922132-115922202 | Common:1; Rare:8 | ||||
| chr11:115925013-115925070 | Common:1; Rare:12 | ||||
| chr11:115925074-115925392 | Rare:56 | ||||
| chr11:115926206-115926442 | Common:3; Rare:58 | ||||
| chr11:115928155-115928269 | Rare:27 | ||||
| chr11:115929647-115929873 | Common:1; Rare:38 | ||||
| chr11:115931092-115931383 | Common:2; Rare:61 | ||||
| chr11:116835928-116836183 | Rare:98; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):7 | ||||
| chr11:116853643-116853849 | Rare:37 |