| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:154682894-154682997 | Rare:31 | ||||
| chr5:157574631-157574801 | Common:4; Rare:46 | ||||
| chr5:159100301-159100575 | Common:3; Rare:83 | ||||
| chr5:170275831-170276126 | Common:1; Rare:61 | ||||
| chr5:172656726-172656896 | Common:1; Rare:29 | ||||
| chr5:172766474-172766676 | Common:1; Rare:50 | ||||
| chr5:172769904-172769926 | Rare:5 | ||||
| chr5:177489150-177489557 | Common:1; Rare:134 | ||||
| chr5:177489569-177489809 | Common:1; Rare:74 | ||||
| chr5:178206497-178206753 | Common:2; Rare:77 | ||||
| chr5:178213886-178213938 | Rare:9 | ||||
| chr5:179829082-179829204 | Common:1; Rare:23 | ||||
| chr5:179832836-179833234 | Common:11; Rare:158; Clinvar:7; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr5:180831582-180831699 | Common:2; Rare:51 | ||||
| chr5:181206811-181207117 | Common:9; Rare:148 |