| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:118951838-118952185 | Common:1; Rare:96; Clinvar:7; Clinvar (benign):1 | ||||
| chr8:119832815-119832897 | Common:1; Rare:32 | ||||
| chr8:120445074-120445449 | Common:1; Rare:97 | ||||
| chr8:120811075-120811248 | Common:3; Rare:57 | ||||
| chr8:123274243-123274307 | Rare:3 | ||||
| chr8:123396388-123396504 | Common:1; Rare:63 | ||||
| chr8:123416528-123416830 | Rare:81 | ||||
| chr8:124474521-124474781 | Common:1; Rare:97 | ||||
| chr8:124538979-124539275 | Common:2; Rare:156; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr8:124998226-124998700 | Common:5; Rare:193 | ||||
| chr8:125091633-125091934 | Common:2; Rare:103; Clinvar:1; Clinvar (benign):4 | ||||
| chr8:133297163-133297507 | Common:3; Rare:131; Clinvar:4; Clinvar (benign):1 | ||||
| chr8:133571827-133572276 | Rare:116 | ||||
| chr8:140511020-140511497 | Common:4; Rare:160 | ||||
| chr8:141128280-141128654 | Common:5; Rare:117 |