| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:13548983-13549177 | Common:1; Rare:63 | ||||
| chr3:14124736-14125179 | Common:4; Rare:128; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178564-14178867 | Common:2; Rare:158; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:14947258-14947554 | Common:3; Rare:134 | ||||
| chr3:15427490-15427623 | Common:1; Rare:48 | ||||
| chr3:15601502-15601804 | Common:4; Rare:125; Clinvar:1 | ||||
| chr3:16264878-16265220 | Common:2; Rare:110 | ||||
| chr3:17742596-17742952 | Common:4; Rare:124 | ||||
| chr3:19946974-19947433 | Common:7; Rare:169 | ||||
| chr3:21751113-21751405 | Common:3; Rare:92 | ||||
| chr3:23916911-23917214 | Rare:115 | ||||
| chr3:23917645-23917946 | Common:2; Rare:81; Clinvar (benign):1 | ||||
| chr3:25783383-25783634 | Common:2; Rare:81; Clinvar (benign):3 | ||||
| chr3:25789789-25790118 | Common:5; Rare:108 | ||||
| chr3:28348973-28349203 | Common:3; Rare:68 |