| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:151253081-151253261 | Common:2; Rare:56; Clinvar:1; Clinvar (benign):2 | ||||
| chr5:151686877-151687057 | Common:1; Rare:40 | ||||
| chr5:151771662-151771981 | Common:3; Rare:108 | ||||
| chr5:151772147-151772301 | Rare:45 | ||||
| chr5:154038856-154039043 | Common:1; Rare:68 | ||||
| chr5:154478227-154478563 | Common:1; Rare:78 | ||||
| chr5:154850526-154850540 | Rare:5 | ||||
| chr5:154850556-154850721 | Common:1; Rare:30 | ||||
| chr5:154857719-154857897 | Rare:43 | ||||
| chr5:154858067-154858254 | Common:6; Rare:59 | ||||
| chr5:154858394-154858730 | Common:1; Rare:113 | ||||
| chr5:154941031-154941146 | Common:1; Rare:57 | ||||
| chr5:157266009-157266183 | Common:1; Rare:49 | ||||
| chr5:157269214-157269380 | Rare:25 | ||||
| chr5:157575747-157575956 | Common:3; Rare:53 |