| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:96764942-96765325 | Common:2; Rare:78 | ||||
| chr5:96934756-96934870 | Rare:27 | ||||
| chr5:112419905-112420229 | Common:5; Rare:144 | ||||
| chr5:128083025-128083160 | Common:2; Rare:41 | ||||
| chr5:137800985-137801447 | Common:10; Rare:81 | ||||
| chr5:137808509-137809393 | Common:3; Rare:194 | ||||
| chr5:137809981-137810115 | Rare:21 | ||||
| chr5:146068292-146068468 | Common:1; Rare:33 | ||||
| chr5:148826305-148826632 | Common:4; Rare:74 | ||||
| chr5:149694109-149694245 | Common:1; Rare:26 | ||||
| chr5:150778568-150778864 | Common:5; Rare:102 | ||||
| chr5:170747431-170747723 | Common:1; Rare:54 | ||||
| chr5:179530716-179530829 | Rare:30 | ||||
| chr5:179833338-179833650 | Common:6; Rare:100; Clinvar:2; Clinvar (benign):2 | ||||
| chr5:180830875-180831027 | Common:1; Rare:49 |