| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:119596839-119597399 | Common:6; Rare:139 | ||||
| chr10:119651000-119651591 | Common:8; Rare:190; Clinvar:1; Clinvar (benign):5 | ||||
| chr10:119725706-119726192 | Common:4; Rare:161 | ||||
| chr10:119726286-119726304 | Rare:8 | ||||
| chr10:119726338-119726538 | Common:2; Rare:54 | ||||
| chr10:119872075-119872592 | Common:4; Rare:151 | ||||
| chr10:119872667-119873146 | Common:4; Rare:159 | ||||
| chr10:119892327-119892368 | Rare:10 | ||||
| chr10:119892471-119892846 | Common:3; Rare:136 | ||||
| chr10:120851144-120851223 | Rare:23 | ||||
| chr10:120851232-120851609 | Common:7; Rare:136 | ||||
| chr10:121596091-121596301 | Common:2; Rare:34 | ||||
| chr10:121598342-121598877 | Common:5; Rare:151; Clinvar:2 | ||||
| chr10:121927375-121927614 | Rare:45 | ||||
| chr10:121927835-121928500 | Common:3; Rare:215 |