| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:119164220-119165070 | Common:12; Rare:266 | ||||
| chr10:119165273-119165958 | Common:18; Rare:850; Clinvar:2; Clinvar (benign):25 | ||||
| chr10:119174357-119175606 | Common:8; Rare:315 | ||||
| chr10:119178369-119179062 | Common:22; Rare:645 | ||||
| chr10:119207290-119207750 | Common:9; Rare:433 | ||||
| chr10:119516260-119517100 | Common:9; Rare:248 | ||||
| chr10:119542540-119542940 | Common:21; Rare:371 | ||||
| chr10:119543024-119543424 | Common:3; Rare:89 | ||||
| chr10:119595565-119596918 | Common:10; Rare:829 | ||||
| chr10:119596864-119597395 | Common:21; Rare:868 | ||||
| chr10:119651110-119651620 | Common:38; Rare:740; Clinvar:6; Clinvar (benign):25 | ||||
| chr10:119651723-119652123 | Common:3; Rare:115; Clinvar:6; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr10:119725695-119726293 | Common:23; Rare:1023 | ||||
| chr10:119726227-119726637 | Common:6; Rare:234 | ||||
| chr10:119872746-119873146 | Common:19; Rare:529 |