| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:11783448-11783888 | Common:7; Rare:112 | ||||
| chr1:11908865-11909104 | Common:4; Rare:100 | ||||
| chr1:11909703-11909962 | Common:20; Rare:190 | ||||
| chr1:11914939-11915423 | Common:13; Rare:193 | ||||
| chr1:11924910-11925660 | Common:3; Rare:273 | ||||
| chr1:11929800-11930340 | Common:7; Rare:150 | ||||
| chr1:11930553-11930953 | Common:1; Rare:69 | ||||
| chr1:12004590-12004890 | Common:1; Rare:66; Clinvar:4; Clinvar (benign):1 | ||||
| chr1:12004910-12005160 | Common:1; Rare:50; Clinvar (benign):1 | ||||
| chr1:12005509-12006207 | Common:6; Rare:184; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr1:12038272-12038672 | Common:2; Rare:128 | ||||
| chr1:12039110-12039470 | Common:1; Rare:69 | ||||
| chr1:12039774-12040174 | Common:2; Rare:80 | ||||
| chr1:12040238-12041073 | Common:16; Rare:453 | ||||
| chr1:12044026-12044426 | Common:5; Rare:99 |