| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:33440606-33441108 | Common:7; Rare:140 | ||||
| chr5:34656023-34656473 | Common:4; Rare:127 | ||||
| chr5:34686776-34686916 | Common:1; Rare:27 | ||||
| chr5:34915486-34915752 | Common:1; Rare:66 | ||||
| chr5:35230323-35230343 | Rare:4 | ||||
| chr5:35617712-35617920 | Common:1; Rare:37 | ||||
| chr5:36151882-36152174 | Rare:91 | ||||
| chr5:36876625-36876864 | Common:1; Rare:70; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:38845774-38846085 | Common:1; Rare:80 | ||||
| chr5:39074370-39074522 | Common:1; Rare:69 | ||||
| chr5:40679717-40679929 | Common:1; Rare:43 | ||||
| chr5:40755901-40756018 | Rare:33 | ||||
| chr5:40798151-40798428 | Common:1; Rare:106 | ||||
| chr5:40835184-40835325 | Common:2; Rare:61 | ||||
| chr5:41904029-41904389 | Common:2; Rare:116 |