| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:150155867-150155971 | Rare:38 | ||||
| chr5:150357503-150357749 | Rare:75; Clinvar:2; Clinvar (benign):4 | ||||
| chr5:150449436-150449802 | Common:5; Rare:98 | ||||
| chr5:150640537-150640732 | Rare:36 | ||||
| chr5:150700949-150701165 | Common:2; Rare:87 | ||||
| chr5:150758989-150759139 | Common:2; Rare:61 | ||||
| chr5:150904781-150904919 | Common:1; Rare:33 | ||||
| chr5:150904921-150905230 | Common:2; Rare:74 | ||||
| chr5:151080935-151081219 | Common:2; Rare:96 | ||||
| chr5:151157692-151158135 | Common:3; Rare:93 | ||||
| chr5:151224073-151224141 | Common:1; Rare:23 | ||||
| chr5:151771404-151771738 | Common:1; Rare:106 | ||||
| chr5:154038860-154039010 | Common:1; Rare:56 | ||||
| chr5:154287224-154287470 | Common:2; Rare:38 | ||||
| chr5:154445802-154445971 | Common:1; Rare:39 |