| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:109409811-109410196 | Common:4; Rare:138 | ||||
| chr5:109689269-109689434 | Common:4; Rare:79 | ||||
| chr5:110738895-110739137 | Common:2; Rare:98; Clinvar (pathogenic):1 | ||||
| chr5:111092181-111092432 | Common:2; Rare:128; Clinvar:2; Clinvar (benign):4 | ||||
| chr5:111224143-111224591 | Rare:175 | ||||
| chr5:111512440-111512847 | Common:4; Rare:137 | ||||
| chr5:111756229-111756324 | Common:1; Rare:8 | ||||
| chr5:111757146-111757292 | Common:5; Rare:27 | ||||
| chr5:111757318-111757345 | Rare:6 | ||||
| chr5:111757378-111757856 | Common:1; Rare:175 | ||||
| chr5:111757946-111758129 | Common:2; Rare:65 | ||||
| chr5:112707428-112707825 | Common:7; Rare:162; Clinvar:78; Clinvar (benign):17; Clinvar (pathogenic):1 | ||||
| chr5:112737740-112738244 | Rare:108; Clinvar:4; Clinvar (benign):5 | ||||
| chr5:112861166-112861392 | Common:5; Rare:88 | ||||
| chr5:112922180-112922562 | Common:2; Rare:137 |