| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:133968598-133968738 | Rare:46 | ||||
| chr5:134004508-134004877 | Common:2; Rare:127 | ||||
| chr5:134371025-134371187 | Common:1; Rare:43 | ||||
| chr5:134648718-134648848 | Rare:35 | ||||
| chr5:135351257-135351537 | Common:1; Rare:51 | ||||
| chr5:135399159-135399310 | Rare:37 | ||||
| chr5:136029045-136029187 | Rare:49 | ||||
| chr5:138178953-138179178 | Common:2; Rare:47 | ||||
| chr5:138543104-138543499 | Common:2; Rare:118 | ||||
| chr5:138753282-138753481 | Common:2; Rare:67 | ||||
| chr5:139561737-139561797 | Rare:26 | ||||
| chr5:140564312-140564846 | Common:1; Rare:136 | ||||
| chr5:140647588-140647880 | Common:5; Rare:120; Clinvar:4; Clinvar (benign):3 | ||||
| chr5:140691263-140691614 | Common:2; Rare:126; Clinvar:10; Clinvar (benign):1 | ||||
| chr5:141320732-141320910 | Common:2; Rare:59 |