| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:97920870-97921244 | Common:2; Rare:129; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr1:97921413-97921513 | Common:1; Rare:21 | ||||
| chr1:98661553-98661739 | Common:2; Rare:65 | ||||
| chr1:99766501-99766736 | Common:1; Rare:43 | ||||
| chr1:99849904-99850458 | Common:2; Rare:156; Clinvar:3; Clinvar (benign):2 | ||||
| chr1:99969724-99970115 | Common:1; Rare:85 | ||||
| chr1:99970448-99970523 | Rare:21 | ||||
| chr1:100037915-100038277 | Common:1; Rare:134 | ||||
| chr1:100038297-100038403 | Common:2; Rare:25 | ||||
| chr1:100038505-100039018 | Common:5; Rare:153 | ||||
| chr1:100132615-100132770 | Common:1; Rare:39 | ||||
| chr1:100132833-100133402 | Common:5; Rare:225 | ||||
| chr1:100249583-100249632 | Common:1; Rare:8 | ||||
| chr1:100249761-100250077 | Common:4; Rare:105; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr1:100266047-100266369 | Common:3; Rare:111 |