| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:149063039-149063254 | Rare:51; Clinvar:1 | ||||
| chr5:149345371-149345632 | Common:1; Rare:105 | ||||
| chr5:149379536-149379683 | Common:1; Rare:28 | ||||
| chr5:149550275-149550318 | Rare:6 | ||||
| chr5:149550354-149550684 | Common:2; Rare:58 | ||||
| chr5:149550840-149551225 | Rare:98 | ||||
| chr5:149551228-149551635 | Common:2; Rare:92 | ||||
| chr5:149960504-149960876 | Common:2; Rare:139; Clinvar:7 | ||||
| chr5:150055290-150055573 | Common:2; Rare:57; Clinvar (pathogenic):1 | ||||
| chr5:150155561-150155858 | Common:1; Rare:73 | ||||
| chr5:150449676-150449795 | Common:4; Rare:42 | ||||
| chr5:150486182-150486313 | Common:1; Rare:26 | ||||
| chr5:150700969-150701156 | Common:2; Rare:77 | ||||
| chr5:150758966-150759084 | Common:2; Rare:53 | ||||
| chr5:151020332-151020740 | Common:2; Rare:103 |