| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:72955869-72956080 | Common:1; Rare:92 | ||||
| chr5:73498359-73498531 | Common:1; Rare:54 | ||||
| chr5:73565629-73565820 | Common:4; Rare:91 | ||||
| chr5:73813195-73813591 | Common:1; Rare:78 | ||||
| chr5:74640548-74640659 | Common:1; Rare:31 | ||||
| chr5:74640719-74640826 | Rare:29 | ||||
| chr5:74767038-74767340 | Common:3; Rare:90 | ||||
| chr5:75336919-75337270 | Common:3; Rare:119 | ||||
| chr5:75511599-75511913 | Common:1; Rare:113 | ||||
| chr5:75717385-75717657 | Common:5; Rare:66 | ||||
| chr5:76715963-76716153 | Common:5; Rare:64 | ||||
| chr5:76818891-76819093 | Common:3; Rare:58 | ||||
| chr5:78360365-78360666 | Common:5; Rare:116 | ||||
| chr5:79069627-79069775 | Rare:51; Clinvar (benign):2 | ||||
| chr5:79991231-79991307 | Rare:24 |