| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:103258477-103258819 | Common:1; Rare:113 | ||||
| chr5:103562702-103562893 | Common:7; Rare:71 | ||||
| chr5:108748673-108748996 | Common:2; Rare:112 | ||||
| chr5:108924443-108924637 | Common:1; Rare:40 | ||||
| chr5:109409866-109410134 | Common:4; Rare:106 | ||||
| chr5:109689163-109689405 | Common:3; Rare:92 | ||||
| chr5:110738895-110739056 | Common:1; Rare:52 | ||||
| chr5:110753004-110753206 | Common:3; Rare:33 | ||||
| chr5:111511969-111512256 | Common:2; Rare:76 | ||||
| chr5:111512390-111512411 | Rare:3 | ||||
| chr5:111512414-111512781 | Common:3; Rare:134 | ||||
| chr5:111757145-111757452 | Common:6; Rare:74 | ||||
| chr5:111757530-111757815 | Common:1; Rare:112 | ||||
| chr5:112737643-112737912 | Rare:65; Clinvar:1; Clinvar (benign):4 | ||||
| chr5:112861091-112861418 | Common:5; Rare:129 |