| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:132557505-132557744 | Common:3; Rare:79 | ||||
| chr5:132557663-132558063 | Common:1; Rare:82 | ||||
| chr5:132737439-132737839 | Common:1; Rare:527 | ||||
| chr5:132760602-132761130 | Common:11; Rare:291 | ||||
| chr5:132774996-132775807 | Common:6; Rare:179 | ||||
| chr5:132775960-132776850 | Common:16; Rare:333 | ||||
| chr5:132777145-132777613 | Common:6; Rare:404 | ||||
| chr5:132777720-132778204 | Common:2; Rare:227 | ||||
| chr5:132778212-132779097 | Common:12; Rare:246 | ||||
| chr5:132807350-132807770 | Common:2; Rare:247 | ||||
| chr5:132829876-132830276 | Common:6; Rare:169 | ||||
| chr5:132830450-132830830 | Rare:359 | ||||
| chr5:132830840-132831291 | Common:1; Rare:209 | ||||
| chr5:132866237-132866737 | Common:10; Rare:599; Clinvar:5; Clinvar (benign):6 | ||||
| chr5:132866864-132867786 | Common:7; Rare:494; Clinvar:10; Clinvar (benign):12; Clinvar (pathogenic):2 |