| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:121961690-121962035 | Common:15; Rare:123 | ||||
| chr5:122129454-122129583 | Common:1; Rare:35 | ||||
| chr5:122774898-122775160 | Rare:108 | ||||
| chr5:122845291-122845625 | Common:3; Rare:114 | ||||
| chr5:123511931-123512268 | Common:1; Rare:107 | ||||
| chr5:124745093-124745263 | Common:1; Rare:42 | ||||
| chr5:124745990-124746176 | Common:1; Rare:43 | ||||
| chr5:124746571-124746680 | Rare:24 | ||||
| chr5:124748758-124749051 | Common:3; Rare:65 | ||||
| chr5:126423266-126423590 | Rare:81 | ||||
| chr5:126595176-126595327 | Common:2; Rare:73; Clinvar:5; Clinvar (benign):7 | ||||
| chr5:126600847-126600998 | Common:1; Rare:73 | ||||
| chr5:127030492-127030793 | Common:3; Rare:78 | ||||
| chr5:127290652-127290886 | Rare:48 | ||||
| chr5:127517359-127517732 | Common:7; Rare:139 |