| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:43065058-43065143 | Common:1; Rare:25 | ||||
| chr5:43067349-43067560 | Rare:35 | ||||
| chr5:43121420-43121648 | Common:1; Rare:86 | ||||
| chr5:43483837-43483959 | Common:1; Rare:43 | ||||
| chr5:43602883-43603258 | Rare:91 | ||||
| chr5:44808711-44808976 | Common:2; Rare:87 | ||||
| chr5:50666881-50666968 | Common:1; Rare:26 | ||||
| chr5:50667324-50667570 | Common:1; Rare:80 | ||||
| chr5:52787820-52788006 | Common:1; Rare:35 | ||||
| chr5:52989187-52989365 | Common:4; Rare:52; Clinvar (benign):1 | ||||
| chr5:53109716-53109862 | Rare:77; Clinvar:3 | ||||
| chr5:54310513-54310711 | Rare:63 | ||||
| chr5:55307625-55308071 | Common:5; Rare:160 | ||||
| chr5:55994789-55995182 | Rare:129 | ||||
| chr5:56909482-56909623 | Common:1; Rare:38 |