| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:10249869-10250157 | Common:16; Rare:138 | ||||
| chr5:10353573-10353917 | Common:3; Rare:132 | ||||
| chr5:10761059-10761465 | Common:14; Rare:136 | ||||
| chr5:16465694-16465902 | Rare:42 | ||||
| chr5:31532037-31532370 | Common:3; Rare:96 | ||||
| chr5:31854747-31855000 | Common:1; Rare:81 | ||||
| chr5:32174247-32174428 | Common:2; Rare:67 | ||||
| chr5:33440606-33441134 | Common:7; Rare:147 | ||||
| chr5:34007976-34008220 | Common:3; Rare:95; Clinvar:2; Clinvar (benign):2 | ||||
| chr5:34656159-34656497 | Common:3; Rare:83 | ||||
| chr5:34839264-34839398 | Common:2; Rare:40 | ||||
| chr5:34915208-34915355 | Rare:40 | ||||
| chr5:34915438-34915753 | Common:1; Rare:81 | ||||
| chr5:34929677-34930045 | Common:1; Rare:112 | ||||
| chr5:35856803-35856953 | Rare:24 |