| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:119596911-119596988 | Common:1; Rare:19 | ||||
| chr10:119597005-119597138 | Rare:30 | ||||
| chr10:119651243-119651417 | Common:6; Rare:68; Clinvar:1; Clinvar (benign):4 | ||||
| chr10:119651745-119651852 | Common:1; Rare:41; Clinvar:4; Clinvar (benign):2 | ||||
| chr10:119818610-119818749 | Rare:46 | ||||
| chr10:119892548-119892779 | Common:3; Rare:88 | ||||
| chr10:120851200-120851453 | Common:5; Rare:97 | ||||
| chr10:121597963-121598012 | Common:1; Rare:7; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:121927904-121928068 | Common:1; Rare:63 | ||||
| chr10:121928459-121928522 | Rare:15 | ||||
| chr10:121974530-121974591 | Common:1; Rare:14 | ||||
| chr10:121974690-121974867 | Common:2; Rare:53 | ||||
| chr10:122019464-122019863 | Common:5; Rare:62 | ||||
| chr10:122290896-122291068 | Common:4; Rare:31 | ||||
| chr10:122374425-122374793 | Common:2; Rare:118 |