| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:139482649-139482812 | Rare:24 | ||||
| chr5:139561100-139561358 | Common:1; Rare:101 | ||||
| chr5:139561728-139561802 | Rare:30 | ||||
| chr5:140175011-140175241 | Rare:62 | ||||
| chr5:140557397-140557537 | Common:1; Rare:92 | ||||
| chr5:140564318-140564470 | Common:1; Rare:44 | ||||
| chr5:140564556-140564838 | Rare:74 | ||||
| chr5:140647540-140647889 | Common:5; Rare:147; Clinvar:4; Clinvar (benign):5 | ||||
| chr5:140664713-140664907 | Common:3; Rare:48 | ||||
| chr5:140691313-140691655 | Common:1; Rare:122; Clinvar:10; Clinvar (benign):1 | ||||
| chr5:141320742-141320910 | Common:1; Rare:56 | ||||
| chr5:141636800-141636989 | Common:2; Rare:90 | ||||
| chr5:141923613-141923930 | Common:1; Rare:98 | ||||
| chr5:142324973-142325197 | Rare:82 | ||||
| chr5:144170557-144170839 | Common:2; Rare:91 |