| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:150357465-150357743 | Rare:90; Clinvar:2; Clinvar (benign):4 | ||||
| chr5:150412684-150413123 | Common:2; Rare:83 | ||||
| chr5:150449676-150449797 | Common:4; Rare:43 | ||||
| chr5:150700981-150701126 | Common:2; Rare:64 | ||||
| chr5:151080949-151081204 | Common:1; Rare:86 | ||||
| chr5:151157699-151158007 | Common:2; Rare:68 | ||||
| chr5:151224015-151224162 | Common:3; Rare:45 | ||||
| chr5:151252966-151253255 | Common:2; Rare:80; Clinvar:1; Clinvar (benign):2 | ||||
| chr5:154038878-154039010 | Common:1; Rare:47 | ||||
| chr5:154858394-154858698 | Common:1; Rare:101 | ||||
| chr5:154938186-154938246 | Rare:19 | ||||
| chr5:157266026-157266183 | Common:1; Rare:46 | ||||
| chr5:157269214-157269407 | Rare:28 | ||||
| chr5:157731349-157731469 | Common:4; Rare:47 | ||||
| chr5:157731651-157731889 | Common:2; Rare:88 |