| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:113515114-113515275 | Rare:51 | ||||
| chr3:113696529-113696933 | Rare:132 | ||||
| chr3:113746156-113746401 | Rare:100 | ||||
| chr3:113746962-113747120 | Common:3; Rare:25 | ||||
| chr3:114056481-114056848 | Common:2; Rare:137 | ||||
| chr3:114454589-114455043 | Common:4; Rare:49 | ||||
| chr3:115147241-115147407 | Common:1; Rare:39 | ||||
| chr3:115623141-115623719 | Common:4; Rare:136 | ||||
| chr3:116445448-116445741 | Common:1; Rare:54 | ||||
| chr3:119240855-119240952 | Common:1; Rare:33 | ||||
| chr3:119463604-119463781 | Common:3; Rare:49 | ||||
| chr3:119468826-119469105 | Common:1; Rare:105; Clinvar (pathogenic):1 | ||||
| chr3:119498356-119498723 | Common:5; Rare:119 | ||||
| chr3:119677318-119677536 | Common:1; Rare:77 | ||||
| chr3:120093465-120093512 | Rare:19 |