| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:64270432-64270565 | Rare:31 | ||||
| chr11:64284509-64284883 | Common:1; Rare:136 | ||||
| chr11:64285800-64285996 | Rare:56 | ||||
| chr11:64305224-64305599 | Common:1; Rare:91 | ||||
| chr11:64306086-64306401 | Rare:66 | ||||
| chr11:64317093-64317650 | Common:3; Rare:233 | ||||
| chr11:64317653-64318348 | Common:4; Rare:221 | ||||
| chr11:64342564-64342762 | Common:1; Rare:57 | ||||
| chr11:64643498-64643803 | Common:3; Rare:70 | ||||
| chr11:64742173-64742490 | Rare:84 | ||||
| chr11:64769226-64769557 | Common:1; Rare:71 | ||||
| chr11:64777727-64777874 | Common:1; Rare:71 | ||||
| chr11:64778364-64779052 | Common:5; Rare:269 | ||||
| chr11:64810495-64810827 | Common:3; Rare:79; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:64878487-64878849 | Common:4; Rare:140 |