| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:156130290-156130650 | Common:2; Rare:91; Clinvar:3; Clinvar (benign):2 | ||||
| chr1:156148392-156148855 | Common:5; Rare:122 | ||||
| chr1:156151402-156151802 | Common:1; Rare:70 | ||||
| chr1:156157499-156157916 | Common:2; Rare:111 | ||||
| chr1:156159044-156159444 | Common:6; Rare:121 | ||||
| chr1:156217929-156218329 | Common:1; Rare:66 | ||||
| chr1:156281438-156281915 | Common:3; Rare:129 | ||||
| chr1:156456510-156456905 | Common:4; Rare:198 | ||||
| chr1:156457206-156457746 | Common:5; Rare:242 | ||||
| chr1:156481503-156481903 | Common:1; Rare:92 | ||||
| chr1:156487900-156488565 | Common:2; Rare:185 | ||||
| chr1:156488470-156488820 | Common:4; Rare:88 | ||||
| chr1:156489112-156489375 | Common:1; Rare:70 | ||||
| chr1:156491612-156492032 | Common:3; Rare:121 | ||||
| chr1:156492267-156492529 | Rare:49 |