| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:27251208-27251829 | Common:12; Rare:195 | ||||
| chr13:27270692-27270838 | Rare:50 | ||||
| chr13:27424499-27424942 | Common:4; Rare:145 | ||||
| chr13:27449964-27450100 | Rare:35 | ||||
| chr13:27450109-27450246 | Common:3; Rare:47 | ||||
| chr13:27450383-27450685 | Common:4; Rare:113 | ||||
| chr13:27620544-27620879 | Common:2; Rare:105 | ||||
| chr13:28138119-28138234 | Common:1; Rare:38 | ||||
| chr13:28138298-28138595 | Common:3; Rare:83 | ||||
| chr13:28139266-28139637 | Common:1; Rare:87 | ||||
| chr13:28494978-28495256 | Common:1; Rare:77 | ||||
| chr13:28659049-28659184 | Rare:59; Clinvar (pathogenic):1 | ||||
| chr13:29595608-29596082 | Common:4; Rare:145 | ||||
| chr13:29850492-29850747 | Common:2; Rare:91 | ||||
| chr13:30306813-30307228 | Common:7; Rare:117 |