| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:43067160-43067334 | Rare:33 | ||||
| chr5:43067438-43067562 | Rare:25 | ||||
| chr5:43121404-43121655 | Common:1; Rare:96 | ||||
| chr5:43313388-43313674 | Common:3; Rare:75 | ||||
| chr5:43483837-43483980 | Common:1; Rare:48 | ||||
| chr5:43515120-43515307 | Common:3; Rare:74 | ||||
| chr5:43603068-43603266 | Rare:51 | ||||
| chr5:44808727-44808975 | Common:2; Rare:84 | ||||
| chr5:50667768-50667924 | Common:1; Rare:50 | ||||
| chr5:52787823-52787993 | Common:1; Rare:32 | ||||
| chr5:52988996-52989376 | Common:5; Rare:105; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:53109716-53109890 | Common:1; Rare:89; Clinvar:3 | ||||
| chr5:54310471-54310711 | Rare:73 | ||||
| chr5:55160090-55160250 | Rare:49 | ||||
| chr5:55307631-55308016 | Common:4; Rare:130 |