| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:40666105-40666122 | Rare:2 | ||||
| chr13:40666531-40666992 | Common:3; Rare:151 | ||||
| chr13:40770466-40770756 | Rare:41 | ||||
| chr13:40770923-40770975 | Rare:20 | ||||
| chr13:40771120-40771456 | Common:3; Rare:101 | ||||
| chr13:40789289-40789736 | Common:4; Rare:147; Clinvar:6; Clinvar (benign):2 | ||||
| chr13:40789748-40789906 | Rare:37 | ||||
| chr13:41019075-41019135 | Rare:8 | ||||
| chr13:41019250-41019455 | Rare:32 | ||||
| chr13:41019697-41019807 | Rare:17 | ||||
| chr13:41060175-41060568 | Common:3; Rare:141 | ||||
| chr13:41060843-41061182 | Common:17; Rare:169 | ||||
| chr13:41061217-41061954 | Common:4; Rare:263 | ||||
| chr13:41132504-41132551 | Rare:16 | ||||
| chr13:41132688-41133058 | Common:1; Rare:91 |