| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:236281943-236282258 | Common:6; Rare:93 | ||||
| chr1:236604461-236604611 | Common:4; Rare:48 | ||||
| chr1:236795088-236795420 | Common:5; Rare:139; Clinvar:3 | ||||
| chr1:240091832-240092021 | Common:4; Rare:60 | ||||
| chr1:241519674-241519923 | Common:2; Rare:83; Clinvar:11; Clinvar (benign):5; Clinvar (pathogenic):3 | ||||
| chr1:241848094-241848233 | Common:2; Rare:29 | ||||
| chr1:243254465-243254533 | Common:2; Rare:10 | ||||
| chr1:243254629-243254962 | Common:2; Rare:100 | ||||
| chr1:243255040-243255450 | Common:1; Rare:98 | ||||
| chr1:243255740-243256113 | Rare:101; Clinvar:4 | ||||
| chr1:243851260-243851321 | Rare:7 | ||||
| chr1:244451638-244452339 | Common:2; Rare:210 | ||||
| chr1:244652944-244653186 | Common:3; Rare:97 | ||||
| chr1:244835158-244835368 | Rare:78 | ||||
| chr1:244835540-244835752 | Common:3; Rare:94; Clinvar (benign):5 |