| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:113073095-113073206 | Rare:41 | ||||
| chr1:113812273-113812579 | Common:2; Rare:121 | ||||
| chr1:113904873-113905392 | Common:7; Rare:152; Clinvar (benign):1 | ||||
| chr1:117929555-117929814 | Common:4; Rare:79 | ||||
| chr1:119140619-119140785 | Common:1; Rare:57 | ||||
| chr1:120176328-120176621 | Common:1; Rare:59 | ||||
| chr1:145823933-145824268 | Rare:121 | ||||
| chr1:145918680-145919013 | Common:2; Rare:74 | ||||
| chr1:145927409-145927644 | Common:1; Rare:66; Clinvar (pathogenic):1 | ||||
| chr1:145964590-145964754 | Rare:38 | ||||
| chr1:147172427-147172744 | Common:1; Rare:85 | ||||
| chr1:148679733-148679912 | Rare:18 | ||||
| chr1:149886639-149887124 | Common:3; Rare:186 | ||||
| chr1:149887915-149888215 | Rare:90 | ||||
| chr1:149927766-149927891 | Common:1; Rare:45; Clinvar (benign):4 |