| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:6359736-6360136 | Common:6; Rare:96 | ||||
| chr1:6393102-6393986 | Common:39; Rare:1213 | ||||
| chr1:6393980-6394320 | Common:4; Rare:134 | ||||
| chr1:6424534-6425231 | Common:11; Rare:358; Clinvar:1 | ||||
| chr1:6440351-6440751 | Common:23; Rare:198; Clinvar (benign):6 | ||||
| chr1:6459790-6460110 | Common:1; Rare:91; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr1:6460350-6460670 | Common:2; Rare:86 | ||||
| chr1:6490368-6490820 | Common:10; Rare:246; Clinvar (benign):3 | ||||
| chr1:6554025-6554839 | Common:46; Rare:689 | ||||
| chr1:6579709-6580109 | Common:23; Rare:521 | ||||
| chr1:6580325-6580926 | Common:8; Rare:215 | ||||
| chr1:6584573-6585120 | Common:4; Rare:144 | ||||
| chr1:6602284-6603420 | Common:25; Rare:1220 | ||||
| chr1:6603459-6603663 | Common:2; Rare:64 | ||||
| chr1:6603620-6603950 | Common:3; Rare:144 |