| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:77086420-77086780 | Common:2; Rare:111 | ||||
| chr5:77087170-77087550 | Rare:99 | ||||
| chr5:77492175-77492384 | Rare:120 | ||||
| chr5:77492430-77492575 | Common:1; Rare:42 | ||||
| chr5:77776228-77776472 | Common:1; Rare:98 | ||||
| chr5:78294581-78294800 | Common:1; Rare:172; Clinvar:2 | ||||
| chr5:78360343-78360670 | Common:10; Rare:250 | ||||
| chr5:78648504-78649039 | Common:7; Rare:295 | ||||
| chr5:78985636-78986161 | Common:5; Rare:159; Clinvar:8; Clinvar (benign):5 | ||||
| chr5:79069572-79069770 | Rare:132; Clinvar (benign):4 | ||||
| chr5:79235918-79236204 | Common:8; Rare:238 | ||||
| chr5:79513974-79514242 | Common:2; Rare:169 | ||||
| chr5:79514516-79514735 | Rare:97 | ||||
| chr5:79612217-79612676 | Rare:230 | ||||
| chr5:79991056-79991354 | Rare:141 |