| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:59172958-59173288 | Common:4; Rare:53 | ||||
| chr11:59615723-59615872 | Common:1; Rare:40 | ||||
| chr11:59668991-59669283 | Rare:103 | ||||
| chr11:60906399-60906800 | Rare:104 | ||||
| chr11:60913843-60914257 | Common:1; Rare:87 | ||||
| chr11:61161402-61161755 | Common:1; Rare:101 | ||||
| chr11:61295300-61295439 | Rare:27 | ||||
| chr11:61333032-61333266 | Rare:82 | ||||
| chr11:61361835-61362049 | Common:2; Rare:51; Clinvar:2 | ||||
| chr11:61362206-61362410 | Common:2; Rare:61; Clinvar:8; Clinvar (benign):1 | ||||
| chr11:61392531-61392649 | Common:2; Rare:41; Clinvar:3; Clinvar (benign):2 | ||||
| chr11:61429892-61430170 | Common:1; Rare:122; Clinvar:3; Clinvar (benign):5 | ||||
| chr11:61792564-61792955 | Common:5; Rare:108 | ||||
| chr11:61816529-61816581 | Rare:10 | ||||
| chr11:61816765-61816876 | Rare:32 |