| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:139198277-139198531 | Rare:83; Clinvar (benign):1 | ||||
| chr5:139439453-139439646 | Common:2; Rare:52 | ||||
| chr5:139561091-139561397 | Common:1; Rare:122 | ||||
| chr5:139561440-139561566 | Rare:54 | ||||
| chr5:139561727-139561803 | Rare:31 | ||||
| chr5:140107590-140107849 | Rare:94 | ||||
| chr5:140175017-140175222 | Rare:56 | ||||
| chr5:140346582-140346882 | Common:1; Rare:81 | ||||
| chr5:140557448-140557548 | Common:2; Rare:59 | ||||
| chr5:140564273-140564462 | Common:2; Rare:58 | ||||
| chr5:140564556-140564856 | Rare:78 | ||||
| chr5:140647583-140647923 | Common:5; Rare:138; Clinvar:4; Clinvar (benign):3 | ||||
| chr5:140691305-140691661 | Common:1; Rare:130; Clinvar:11; Clinvar (benign):2 | ||||
| chr5:141213912-141213982 | Rare:8 | ||||
| chr5:141320742-141320910 | Common:1; Rare:56 |