| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:119653270-119653691 | Common:4; Rare:122 | ||||
| chr10:119654661-119654881 | Common:2; Rare:60 | ||||
| chr10:119655720-119655960 | Rare:73 | ||||
| chr10:119658165-119658634 | Common:11; Rare:259 | ||||
| chr10:119663930-119664420 | Common:6; Rare:167 | ||||
| chr10:119667809-119668517 | Common:12; Rare:306 | ||||
| chr10:119669396-119670087 | Common:12; Rare:290; Clinvar:13; Clinvar (benign):15; Clinvar (pathogenic):2 | ||||
| chr10:119798540-119799257 | Common:4; Rare:251 | ||||
| chr10:119871860-119872130 | Common:6; Rare:113 | ||||
| chr10:120917790-120918450 | Common:6; Rare:124 | ||||
| chr10:120979487-120979632 | Rare:33 | ||||
| chr10:120979720-120980010 | Common:6; Rare:62 | ||||
| chr10:120987014-120987414 | Common:1; Rare:89 | ||||
| chr10:120996597-120997053 | Common:3; Rare:76 | ||||
| chr10:121043195-121043943 | Common:3; Rare:268 |