| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:140564573-140564837 | Rare:73 | ||||
| chr5:140639282-140639478 | Common:3; Rare:49 | ||||
| chr5:140647576-140647914 | Common:5; Rare:139; Clinvar:4; Clinvar (benign):3 | ||||
| chr5:140664770-140664904 | Common:2; Rare:33 | ||||
| chr5:140691317-140691614 | Common:1; Rare:102; Clinvar:8 | ||||
| chr5:140965966-140966170 | Rare:33 | ||||
| chr5:141172537-141172676 | Common:1; Rare:27 | ||||
| chr5:141245219-141245419 | Common:1; Rare:43 | ||||
| chr5:141320732-141320912 | Common:2; Rare:61 | ||||
| chr5:141373716-141373955 | Common:2; Rare:34 | ||||
| chr5:141402571-141402825 | Common:1; Rare:44 | ||||
| chr5:141475622-141475919 | Common:3; Rare:46 | ||||
| chr5:141476355-141476536 | Rare:54 | ||||
| chr5:141484894-141485167 | Common:1; Rare:60 | ||||
| chr5:141636810-141637011 | Common:2; Rare:86 |