| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:140557433-140557537 | Common:1; Rare:64 | ||||
| chr5:140564573-140564838 | Rare:73 | ||||
| chr5:140639302-140639478 | Common:3; Rare:44 | ||||
| chr5:140647594-140648096 | Common:19; Rare:186; Clinvar:4; Clinvar (benign):3 | ||||
| chr5:140691318-140691506 | Common:1; Rare:72; Clinvar:7 | ||||
| chr5:140700279-140700490 | Rare:69 | ||||
| chr5:141094495-141094683 | Rare:44 | ||||
| chr5:141320742-141320875 | Common:1; Rare:42 | ||||
| chr5:141636808-141636997 | Common:2; Rare:83 | ||||
| chr5:141682195-141682310 | Common:1; Rare:36 | ||||
| chr5:141923691-141923881 | Common:1; Rare:51 | ||||
| chr5:144170585-144170860 | Common:2; Rare:87 | ||||
| chr5:145835276-145835539 | Common:3; Rare:63 | ||||
| chr5:146182511-146182864 | Common:4; Rare:101 | ||||
| chr5:146203319-146203739 | Common:4; Rare:129 |