| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:138178946-138179160 | Common:2; Rare:45 | ||||
| chr5:138465774-138465891 | Rare:45 | ||||
| chr5:138543084-138543558 | Common:2; Rare:153 | ||||
| chr5:138753255-138753507 | Common:2; Rare:87 | ||||
| chr5:139198277-139198526 | Rare:82; Clinvar (benign):1 | ||||
| chr5:139273953-139274135 | Rare:83 | ||||
| chr5:139561097-139561413 | Common:1; Rare:126 | ||||
| chr5:139561727-139561809 | Rare:32 | ||||
| chr5:139648199-139648368 | Rare:49 | ||||
| chr5:140107723-140107834 | Rare:32 | ||||
| chr5:140175017-140175275 | Common:1; Rare:63 | ||||
| chr5:140303059-140303162 | Common:1; Rare:35 | ||||
| chr5:140557392-140557548 | Common:3; Rare:101 | ||||
| chr5:140564273-140564849 | Common:2; Rare:150 | ||||
| chr5:140647576-140647924 | Common:5; Rare:143; Clinvar:4; Clinvar (benign):3 |