| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:151771412-151771474 | Rare:27 | ||||
| chr5:151771616-151772000 | Common:4; Rare:139 | ||||
| chr5:154038864-154039010 | Common:1; Rare:52 | ||||
| chr5:154850545-154850738 | Common:1; Rare:35 | ||||
| chr5:154857801-154857889 | Rare:22 | ||||
| chr5:154858466-154858714 | Common:1; Rare:81 | ||||
| chr5:154941029-154941116 | Common:1; Rare:39 | ||||
| chr5:157575748-157575920 | Common:3; Rare:46 | ||||
| chr5:159263201-159263330 | Common:1; Rare:43 | ||||
| chr5:160400026-160400165 | Rare:44 | ||||
| chr5:160419049-160419260 | Common:4; Rare:80 | ||||
| chr5:163460048-163460165 | Common:2; Rare:48 | ||||
| chr5:163460366-163460677 | Common:5; Rare:71 | ||||
| chr5:168486350-168486534 | Common:3; Rare:71; Clinvar (benign):3; Clinvar (pathogenic):3 | ||||
| chr5:171387498-171388006 | Common:1; Rare:239; Clinvar:1 |