| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:156002612-156002744 | Common:1; Rare:17 | ||||
| chr1:156053755-156053956 | Rare:136 | ||||
| chr1:156054548-156054965 | Common:10; Rare:289 | ||||
| chr1:156060975-156061306 | Common:2; Rare:198 | ||||
| chr1:156082390-156082740 | Rare:167 | ||||
| chr1:156106410-156106730 | Common:4; Rare:91 | ||||
| chr1:156114110-156115011 | Common:6; Rare:340; Clinvar:18; Clinvar (benign):12; Clinvar (pathogenic):1 | ||||
| chr1:156134380-156135470 | Common:10; Rare:389; Clinvar:49; Clinvar (benign):35; Clinvar (pathogenic):26 | ||||
| chr1:156153428-156153654 | Common:1; Rare:82; Clinvar:4 | ||||
| chr1:156193670-156194235 | Common:9; Rare:318 | ||||
| chr1:156194431-156195371 | Common:4; Rare:216 | ||||
| chr1:156212752-156213440 | Common:8; Rare:483 | ||||
| chr1:156282445-156282614 | Common:2; Rare:70 | ||||
| chr1:156282604-156283061 | Common:9; Rare:281 | ||||
| chr1:156284140-156284363 | Rare:111 |