| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:112584382-112584646 | Common:1; Rare:73 | ||||
| chr2:112584755-112584856 | Rare:24 | ||||
| chr2:112645688-112645954 | Common:1; Rare:98 | ||||
| chr2:112646243-112646393 | Common:1; Rare:53 | ||||
| chr2:112764575-112764779 | Common:1; Rare:67; Clinvar (pathogenic):1 | ||||
| chr2:113627041-113627303 | Common:3; Rare:78 | ||||
| chr2:113756556-113756791 | Common:3; Rare:82 | ||||
| chr2:113889705-113890321 | Common:9; Rare:193 | ||||
| chr2:118013991-118014264 | Common:3; Rare:139 | ||||
| chr2:118088319-118088516 | Common:1; Rare:61 | ||||
| chr2:119223663-119223862 | Common:1; Rare:58 | ||||
| chr2:119366749-119367090 | Common:1; Rare:106 | ||||
| chr2:119679007-119679248 | Common:4; Rare:66 | ||||
| chr2:119759770-119759872 | Common:1; Rare:30 | ||||
| chr2:120012973-120013111 | Common:1; Rare:67 |