| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:147234835-147235129 | Common:2; Rare:84 | ||||
| chr5:147509930-147510243 | Common:1; Rare:59 | ||||
| chr5:148383744-148384029 | Rare:77 | ||||
| chr5:149063039-149063380 | Rare:70; Clinvar:1 | ||||
| chr5:149345371-149345559 | Common:1; Rare:71 | ||||
| chr5:149550840-149551123 | Rare:69 | ||||
| chr5:149551324-149551645 | Rare:74 | ||||
| chr5:149960564-149961002 | Rare:146; Clinvar:8; Clinvar (pathogenic):1 | ||||
| chr5:150357444-150357760 | Rare:105; Clinvar:2; Clinvar (benign):4 | ||||
| chr5:150412710-150413113 | Common:2; Rare:72 | ||||
| chr5:150449453-150449797 | Common:5; Rare:92 | ||||
| chr5:150700969-150701162 | Common:2; Rare:79 | ||||
| chr5:150758989-150759178 | Common:3; Rare:74 | ||||
| chr5:150904761-150905255 | Common:4; Rare:116 | ||||
| chr5:151080966-151081204 | Common:1; Rare:81 |