| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:64723016-64723416 | Common:5; Rare:147 | ||||
| chr11:64742946-64743113 | Rare:52 | ||||
| chr11:64777693-64777827 | Common:1; Rare:63 | ||||
| chr11:64778463-64778805 | Common:2; Rare:146 | ||||
| chr11:64779119-64779221 | Common:2; Rare:19 | ||||
| chr11:64803147-64803408 | Rare:106 | ||||
| chr11:64803624-64803801 | Rare:50 | ||||
| chr11:64809676-64810076 | Rare:158; Clinvar:38; Clinvar (benign):23; Clinvar (pathogenic):4 | ||||
| chr11:64810505-64810821 | Common:2; Rare:74; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:64844600-64844892 | Common:3; Rare:79 | ||||
| chr11:64855064-64855273 | Common:1; Rare:51 | ||||
| chr11:64856730-64856873 | Rare:32 | ||||
| chr11:64878605-64878912 | Common:2; Rare:101 | ||||
| chr11:64887942-64888172 | Common:1; Rare:65 | ||||
| chr11:64917187-64917438 | Common:2; Rare:64 |