| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:141878355-141878424 | Rare:22 | ||||
| chr5:141878474-141878598 | Common:2; Rare:35 | ||||
| chr5:141923768-141923921 | Rare:49 | ||||
| chr5:142108686-142108930 | Common:2; Rare:79 | ||||
| chr5:142324958-142325322 | Rare:115 | ||||
| chr5:142770324-142770517 | Common:2; Rare:62 | ||||
| chr5:142770825-142770888 | Rare:17 | ||||
| chr5:143404409-143404617 | Common:2; Rare:49 | ||||
| chr5:144170538-144170879 | Common:2; Rare:108 | ||||
| chr5:145835302-145835473 | Common:1; Rare:44 | ||||
| chr5:146142935-146143209 | Common:1; Rare:71; Clinvar (benign):3 | ||||
| chr5:146144329-146144495 | Rare:40; Clinvar (benign):1 | ||||
| chr5:146182477-146182912 | Common:4; Rare:135 | ||||
| chr5:146203378-146203742 | Common:4; Rare:112 | ||||
| chr5:147234862-147235116 | Common:2; Rare:70 |