| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:74640723-74640934 | Common:1; Rare:66 | ||||
| chr5:74767043-74767347 | Common:3; Rare:96 | ||||
| chr5:75236890-75237019 | Common:4; Rare:52 | ||||
| chr5:75336940-75337290 | Common:3; Rare:119 | ||||
| chr5:75511597-75511949 | Common:2; Rare:121 | ||||
| chr5:75717363-75717663 | Common:5; Rare:75 | ||||
| chr5:76953511-76953663 | Rare:44 | ||||
| chr5:77086603-77086736 | Common:1; Rare:30 | ||||
| chr5:77087172-77087307 | Rare:33 | ||||
| chr5:77087806-77088130 | Common:3; Rare:59 | ||||
| chr5:77776211-77776469 | Common:1; Rare:98 | ||||
| chr5:78294621-78294800 | Rare:68; Clinvar:1 | ||||
| chr5:78360355-78360726 | Common:5; Rare:142 | ||||
| chr5:78648504-78648880 | Common:4; Rare:105 | ||||
| chr5:79069590-79069785 | Rare:66; Clinvar (benign):2 |