| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:186727277-186727593 | Rare:46 | ||||
| chr5:285702-285840 | Rare:19 | ||||
| chr5:293100-293160 | Rare:15 | ||||
| chr5:473841-474042 | Common:3; Rare:44 | ||||
| chr5:475578-475782 | Common:1; Rare:67 | ||||
| chr5:476352-476701 | Common:2; Rare:120; Clinvar:1 | ||||
| chr5:479916-480030 | Common:1; Rare:41 | ||||
| chr5:706218-706231 | Rare:2 | ||||
| chr5:784690-784884 | Common:5; Rare:61 | ||||
| chr5:845863-846117 | Common:3; Rare:22 | ||||
| chr5:1060344-1060657 | Common:5; Rare:88 | ||||
| chr5:1077888-1078091 | Common:4; Rare:76 | ||||
| chr5:1199961-1200201 | Rare:57 | ||||
| chr5:1205038-1205305 | Common:4; Rare:76 | ||||
| chr5:1208736-1209093 | Common:7; Rare:122; Clinvar (benign):1 |