| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:56682775-56683070 | Common:2; Rare:118 | ||||
| chr3:56683203-56683370 | Common:2; Rare:62 | ||||
| chr3:56801889-56802055 | Rare:60 | ||||
| chr3:57079204-57079369 | Common:1; Rare:51 | ||||
| chr3:57227591-57227922 | Common:4; Rare:113 | ||||
| chr3:57555996-57556343 | Rare:89 | ||||
| chr3:57597267-57597803 | Common:7; Rare:162 | ||||
| chr3:57633306-57633579 | Rare:40 | ||||
| chr3:57692966-57693170 | Common:1; Rare:60 | ||||
| chr3:57889876-57890096 | Rare:50; Clinvar (benign):2 | ||||
| chr3:58332593-58332977 | Common:10; Rare:83 | ||||
| chr3:58433792-58433976 | Common:1; Rare:77; Clinvar:2; Clinvar (benign):3 | ||||
| chr3:58577317-58577613 | Common:2; Rare:52 | ||||
| chr3:58666592-58667163 | Common:2; Rare:104 | ||||
| chr3:61251308-61251594 | Common:4; Rare:71 |