| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:138933530-138933997 | Common:2; Rare:114; Clinvar:1; Clinvar (benign):2 | ||||
| chr5:140245997-140246253 | Common:1; Rare:50 | ||||
| chr5:140711138-140711275 | Common:1; Rare:38 | ||||
| chr5:147394006-147394365 | Common:4; Rare:95 | ||||
| chr5:147395559-147395853 | Common:4; Rare:74 | ||||
| chr5:148826346-148826632 | Common:4; Rare:69 | ||||
| chr5:148827626-148827821 | Rare:42 | ||||
| chr5:149380779-149381063 | Common:1; Rare:51 | ||||
| chr5:149381492-149381567 | Common:1; Rare:11 | ||||
| chr5:149382154-149382255 | Common:1; Rare:17 | ||||
| chr5:149383494-149383740 | Rare:48 | ||||
| chr5:149406939-149407060 | Rare:18 | ||||
| chr5:149407396-149407621 | Common:2; Rare:44 | ||||
| chr5:149407756-149407964 | Common:3; Rare:32 | ||||
| chr5:149409720-149409890 | Rare:39 |