| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:115625878-115626361 | Common:8; Rare:291 | ||||
| chr5:115841466-115841661 | Common:6; Rare:212 | ||||
| chr5:115841783-115842026 | Common:7; Rare:160 | ||||
| chr5:116084743-116085058 | Common:14; Rare:174 | ||||
| chr5:116085298-116085680 | Common:2; Rare:158 | ||||
| chr5:118988489-118988713 | Common:2; Rare:159 | ||||
| chr5:119070630-119071260 | Common:8; Rare:309 | ||||
| chr5:119268584-119268837 | Common:2; Rare:137 | ||||
| chr5:119452001-119452717 | Common:3; Rare:309; Clinvar:6; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr5:121961793-121962045 | Common:2; Rare:87 | ||||
| chr5:122076674-122076904 | Common:3; Rare:109; Clinvar (benign):2 | ||||
| chr5:122077107-122077295 | Common:1; Rare:33 | ||||
| chr5:122078113-122078442 | Common:2; Rare:137 | ||||
| chr5:122774831-122775158 | Common:2; Rare:240 | ||||
| chr5:122845323-122845646 | Common:6; Rare:216 |