| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:236064973-236065360 | Common:4; Rare:138; Clinvar (pathogenic):1 | ||||
| chr1:236281942-236281994 | Common:1; Rare:19 | ||||
| chr1:236523845-236524024 | Common:2; Rare:48 | ||||
| chr1:236604456-236604624 | Common:4; Rare:53 | ||||
| chr1:241519678-241519954 | Common:2; Rare:90; Clinvar:10; Clinvar (benign):5; Clinvar (pathogenic):3 | ||||
| chr1:241848044-241848204 | Common:1; Rare:46 | ||||
| chr1:243255047-243255331 | Common:1; Rare:64 | ||||
| chr1:243255755-243256128 | Common:1; Rare:105; Clinvar:4; Clinvar (benign):1 | ||||
| chr1:244451813-244452212 | Common:1; Rare:135 | ||||
| chr1:244835031-244835333 | Rare:111 | ||||
| chr1:244835575-244835747 | Common:2; Rare:77; Clinvar (benign):5 | ||||
| chr1:244863706-244863977 | Rare:86; Clinvar:4; Clinvar (benign):5 | ||||
| chr1:244863987-244864260 | Common:1; Rare:85; Clinvar:3; Clinvar (benign):5 | ||||
| chr1:244864264-244864691 | Rare:161 | ||||
| chr1:246566218-246566563 | Common:1; Rare:113 |