| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:93079069-93079303 | Common:3; Rare:100 | ||||
| chr1:93179900-93179939 | Rare:9 | ||||
| chr1:93180053-93180751 | Common:2; Rare:272 | ||||
| chr1:93345727-93345946 | Common:4; Rare:81 | ||||
| chr1:93879144-93879274 | Common:1; Rare:44 | ||||
| chr1:94418228-94418480 | Common:2; Rare:88 | ||||
| chr1:94541641-94541991 | Common:1; Rare:100 | ||||
| chr1:94820151-94820564 | Common:6; Rare:111 | ||||
| chr1:94903132-94903445 | Common:1; Rare:63 | ||||
| chr1:94927024-94927449 | Common:3; Rare:140 | ||||
| chr1:95072855-95073018 | Common:1; Rare:67; Clinvar (benign):2 | ||||
| chr1:95233933-95234236 | Common:5; Rare:89 | ||||
| chr1:98661587-98661891 | Common:2; Rare:105 | ||||
| chr1:99766607-99766674 | Rare:13 | ||||
| chr1:99850006-99850418 | Common:1; Rare:118; Clinvar:3; Clinvar (benign):1 |