| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:70170411-70170749 | Common:4; Rare:108 | ||||
| chr10:70233293-70233695 | Common:6; Rare:127; Clinvar (benign):1 | ||||
| chr10:70404509-70404536 | Rare:9 | ||||
| chr10:70888234-70888350 | Common:2; Rare:28 | ||||
| chr10:70888534-70888633 | Common:1; Rare:33; Clinvar:4; Clinvar (benign):1 | ||||
| chr10:71819465-71819889 | Common:1; Rare:168; Clinvar:5; Clinvar (benign):3 | ||||
| chr10:71851183-71851454 | Common:5; Rare:115; Clinvar:4; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr10:72273709-72274120 | Common:1; Rare:119 | ||||
| chr10:72354869-72355023 | Common:2; Rare:74 | ||||
| chr10:73096739-73097142 | Common:5; Rare:112 | ||||
| chr10:73110186-73110541 | Rare:65 | ||||
| chr10:73167874-73168198 | Common:1; Rare:87 | ||||
| chr10:73252512-73252817 | Common:2; Rare:89; Clinvar:5; Clinvar (benign):2 | ||||
| chr10:73495544-73495779 | Rare:56 | ||||
| chr10:73495818-73496112 | Common:2; Rare:83 |