| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:140564662-140564846 | Rare:56 | ||||
| chr5:140639302-140639478 | Common:3; Rare:44 | ||||
| chr5:140647594-140647883 | Common:5; Rare:116; Clinvar:4; Clinvar (benign):3 | ||||
| chr5:140664750-140664904 | Common:2; Rare:37 | ||||
| chr5:140691313-140691497 | Common:1; Rare:67; Clinvar:7 | ||||
| chr5:140700270-140700469 | Rare:65 | ||||
| chr5:141320742-141320933 | Common:2; Rare:67 | ||||
| chr5:141475846-141476003 | Rare:34 | ||||
| chr5:141636809-141637011 | Common:2; Rare:86 | ||||
| chr5:141651387-141651505 | Rare:32 | ||||
| chr5:141923721-141923881 | Common:1; Rare:39 | ||||
| chr5:141968938-141969213 | Common:3; Rare:85 | ||||
| chr5:142012994-142013064 | Rare:22 | ||||
| chr5:143404414-143404604 | Common:2; Rare:45 | ||||
| chr5:143405130-143405461 | Rare:96 |