| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:115146868-115147059 | Common:4; Rare:86 | ||||
| chr3:115623193-115623717 | Common:4; Rare:126 | ||||
| chr3:116445400-116445712 | Common:1; Rare:60 | ||||
| chr3:119463585-119463780 | Common:5; Rare:57 | ||||
| chr3:119468824-119469037 | Common:1; Rare:80; Clinvar (pathogenic):1 | ||||
| chr3:119498396-119498759 | Common:4; Rare:117 | ||||
| chr3:119498775-119498921 | Rare:55 | ||||
| chr3:119676890-119677121 | Common:14; Rare:71 | ||||
| chr3:119677213-119677305 | Rare:39 | ||||
| chr3:119677373-119677536 | Rare:53 | ||||
| chr3:120093536-120093903 | Rare:101 | ||||
| chr3:120094429-120094781 | Common:4; Rare:112 | ||||
| chr3:120450874-120451143 | Rare:95 | ||||
| chr3:120596249-120596540 | Rare:124 | ||||
| chr3:120742488-120742804 | Common:2; Rare:90 |