| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:47751202-47751602 | Common:5; Rare:116 | ||||
| chr1:47758389-47758819 | Common:1; Rare:159 | ||||
| chr1:47758910-47759310 | Rare:111 | ||||
| chr1:48213597-48213733 | Common:2; Rare:23 | ||||
| chr1:50977360-50977631 | Rare:81 | ||||
| chr1:50977660-50977880 | Common:4; Rare:88 | ||||
| chr1:50977900-50978230 | Common:2; Rare:136 | ||||
| chr1:51517790-51518330 | Common:2; Rare:165 | ||||
| chr1:52365140-52365461 | Common:2; Rare:99 | ||||
| chr1:53326185-53326487 | Common:5; Rare:135 | ||||
| chr1:54273424-54274028 | Common:6; Rare:190 | ||||
| chr1:54488213-54488613 | Common:11; Rare:210 | ||||
| chr1:54883640-54884080 | Rare:91; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr1:55443580-55444101 | Common:6; Rare:141 | ||||
| chr1:56644474-56644770 | Common:1; Rare:92 |