| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:163460039-163460161 | Common:2; Rare:51 | ||||
| chr5:163460269-163460672 | Common:5; Rare:92 | ||||
| chr5:163503200-163503413 | Common:1; Rare:60 | ||||
| chr5:163505399-163505673 | Common:1; Rare:86 | ||||
| chr5:167573826-167574029 | Common:2; Rare:47 | ||||
| chr5:168291180-168291760 | Common:1; Rare:141 | ||||
| chr5:168486250-168486521 | Common:3; Rare:78; Clinvar (benign):3; Clinvar (pathogenic):3 | ||||
| chr5:168528955-168529355 | Common:7; Rare:110 | ||||
| chr5:168579601-168579983 | Common:3; Rare:100 | ||||
| chr5:168844320-168844740 | Rare:115 | ||||
| chr5:168844970-168845116 | Rare:27 | ||||
| chr5:168883220-168883490 | Common:1; Rare:73 | ||||
| chr5:168883505-168883815 | Common:2; Rare:77 | ||||
| chr5:169301020-169301340 | Common:3; Rare:89 | ||||
| chr5:169583576-169583854 | Common:6; Rare:98 |