| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:54723014-54723392 | Common:7; Rare:63 | ||||
| chr5:54728065-54728092 | Rare:4 | ||||
| chr5:54742461-54742477 | Rare:3 | ||||
| chr5:54744253-54744561 | Common:1; Rare:55 | ||||
| chr5:54848890-54848916 | Rare:4 | ||||
| chr5:54883504-54883724 | Common:2; Rare:45 | ||||
| chr5:54895826-54895839 | Rare:1 | ||||
| chr5:55160964-55161155 | Rare:58 | ||||
| chr5:55226467-55226706 | Rare:75; Clinvar:1; Clinvar (benign):3 | ||||
| chr5:55440314-55440411 | Rare:22 | ||||
| chr5:55534212-55534324 | Common:1; Rare:31 | ||||
| chr5:55593204-55593239 | Rare:3 | ||||
| chr5:55593269-55593351 | Rare:13 | ||||
| chr5:55912000-55912094 | Rare:19 | ||||
| chr5:55912238-55912319 | Rare:7 |