| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:236524511-236524608 | Common:1; Rare:21 | ||||
| chr1:236541219-236541506 | Common:1; Rare:55 | ||||
| chr1:236604422-236604572 | Common:4; Rare:49 | ||||
| chr1:236796009-236796295 | Rare:72 | ||||
| chr1:237944766-237945002 | Common:2; Rare:49 | ||||
| chr1:241519620-241519988 | Common:3; Rare:118; Clinvar:15; Clinvar (benign):12; Clinvar (pathogenic):4 | ||||
| chr1:241639967-241639994 | Rare:6 | ||||
| chr1:241848085-241848227 | Common:1; Rare:30 | ||||
| chr1:242524411-242524567 | Common:3; Rare:23 | ||||
| chr1:242524675-242524884 | Common:1; Rare:62 | ||||
| chr1:243255040-243255445 | Common:1; Rare:98 | ||||
| chr1:243255741-243256226 | Common:1; Rare:155; Clinvar:5; Clinvar (benign):1 | ||||
| chr1:244451651-244451953 | Rare:91 | ||||
| chr1:244451972-244452161 | Common:1; Rare:70 | ||||
| chr1:244863616-244864182 | Common:1; Rare:193; Clinvar:8; Clinvar (benign):9; Clinvar (pathogenic):1 |