| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:130166579-130166939 | Common:2; Rare:75 | ||||
| chr10:130175784-130176111 | Common:1; Rare:46 | ||||
| chr10:133274858-133275280 | Common:5; Rare:115 | ||||
| chr10:133400245-133400612 | Common:2; Rare:70 | ||||
| chr11:223749-224099 | Common:18; Rare:87 | ||||
| chr11:400344-400704 | Rare:181 | ||||
| chr11:496691-496825 | Rare:41 | ||||
| chr11:555094-555343 | Common:13; Rare:106 | ||||
| chr11:653989-654158 | Common:4; Rare:64; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:711226-711512 | Common:11; Rare:83 | ||||
| chr11:766817-766904 | Rare:27 | ||||
| chr11:783406-783625 | Common:2; Rare:47 | ||||
| chr11:819403-819608 | Common:2; Rare:85; Clinvar:3 | ||||
| chr11:880901-881008 | Rare:19 | ||||
| chr11:882031-882329 | Common:1; Rare:106 |