| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:119596839-119597373 | Common:4; Rare:136 | ||||
| chr10:119650917-119651063 | Common:1; Rare:37 | ||||
| chr10:119651131-119651617 | Common:8; Rare:160; Clinvar:1; Clinvar (benign):5 | ||||
| chr10:119651801-119651919 | Common:1; Rare:40; Clinvar:4; Clinvar (benign):2 | ||||
| chr10:119725706-119726314 | Common:4; Rare:203 | ||||
| chr10:119872296-119872618 | Common:4; Rare:102 | ||||
| chr10:119872636-119873142 | Common:4; Rare:168 | ||||
| chr10:119873400-119873527 | Rare:40 | ||||
| chr10:119892302-119892430 | Common:1; Rare:34 | ||||
| chr10:119892459-119892825 | Common:3; Rare:132 | ||||
| chr10:120456824-120456996 | Common:2; Rare:47 | ||||
| chr10:120457059-120457266 | Common:1; Rare:65 | ||||
| chr10:120850983-120851497 | Common:10; Rare:156 | ||||
| chr10:120851518-120851646 | Common:1; Rare:37 | ||||
| chr10:121598364-121598659 | Common:2; Rare:100; Clinvar:1 |