| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:43311805-43312135 | Common:2; Rare:111 | ||||
| chr11:43358795-43359097 | Rare:127 | ||||
| chr11:43359106-43359264 | Rare:60 | ||||
| chr11:43680404-43680889 | Common:3; Rare:139 | ||||
| chr11:43880661-43880899 | Common:2; Rare:60 | ||||
| chr11:44066174-44066531 | Common:4; Rare:90 | ||||
| chr11:44096122-44096248 | Rare:41 | ||||
| chr11:45146395-45146658 | Common:3; Rare:62 | ||||
| chr11:45286214-45286413 | Rare:63 | ||||
| chr11:45917796-45918180 | Common:1; Rare:96; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:45922185-45922422 | Common:2; Rare:63 | ||||
| chr11:45924035-45924208 | Rare:42 | ||||
| chr11:45925778-45926115 | Common:2; Rare:76 | ||||
| chr11:45926562-45926874 | Common:1; Rare:113 | ||||
| chr11:46119770-46119957 | Common:1; Rare:53 |