| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:140639164-140639515 | Common:3; Rare:81 | ||||
| chr5:140647590-140647896 | Common:5; Rare:124; Clinvar:4; Clinvar (benign):3 | ||||
| chr5:140691313-140691667 | Common:1; Rare:126; Clinvar:10; Clinvar (benign):2 | ||||
| chr5:141320742-141320921 | Common:1; Rare:62 | ||||
| chr5:141476227-141476266 | Rare:11 | ||||
| chr5:141636810-141636959 | Common:2; Rare:69 | ||||
| chr5:141682187-141682328 | Common:1; Rare:47 | ||||
| chr5:141923526-141923847 | Common:1; Rare:76 | ||||
| chr5:141958180-141958468 | Rare:67 | ||||
| chr5:142013001-142013129 | Rare:39 | ||||
| chr5:142324973-142325183 | Rare:78 | ||||
| chr5:142770171-142770377 | Rare:67 | ||||
| chr5:143404442-143404637 | Common:2; Rare:39 | ||||
| chr5:144170543-144170717 | Common:1; Rare:70 | ||||
| chr5:146182489-146182814 | Common:3; Rare:88 |