| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:119366770-119367095 | Common:1; Rare:102 | ||||
| chr2:119431709-119431881 | Common:4; Rare:43 | ||||
| chr2:119679090-119679234 | Common:4; Rare:46 | ||||
| chr2:119759741-119759833 | Common:1; Rare:19 | ||||
| chr2:119760095-119760226 | Common:1; Rare:24 | ||||
| chr2:120252571-120252964 | Common:3; Rare:130 | ||||
| chr2:121285200-121285340 | Rare:47 | ||||
| chr2:121530340-121530884 | Common:10; Rare:194 | ||||
| chr2:121649394-121649711 | Common:2; Rare:95 | ||||
| chr2:121650075-121650157 | Rare:20 | ||||
| chr2:121736736-121737220 | Common:5; Rare:194 | ||||
| chr2:121755421-121755794 | Common:5; Rare:124 | ||||
| chr2:126655986-126656311 | Common:1; Rare:92; Clinvar:2 | ||||
| chr2:127294088-127294233 | Common:2; Rare:57; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:127387199-127387457 | Common:5; Rare:82 |