| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:112254970-112255160 | Common:1; Rare:80 | ||||
| chr2:112275388-112275666 | Common:1; Rare:98 | ||||
| chr2:112275877-112276000 | Rare:37 | ||||
| chr2:112434574-112434824 | Common:1; Rare:65 | ||||
| chr2:112482008-112482327 | Common:3; Rare:113 | ||||
| chr2:112584326-112584652 | Common:2; Rare:93 | ||||
| chr2:112584737-112584892 | Rare:39 | ||||
| chr2:112585264-112585299 | Rare:3 | ||||
| chr2:112645701-112645948 | Common:1; Rare:92 | ||||
| chr2:112646232-112646378 | Common:2; Rare:48 | ||||
| chr2:112764529-112764859 | Common:2; Rare:112; Clinvar (pathogenic):1 | ||||
| chr2:112784453-112784781 | Rare:71 | ||||
| chr2:113437611-113437913 | Common:4; Rare:116 | ||||
| chr2:113627035-113627314 | Common:4; Rare:82 | ||||
| chr2:113756477-113756799 | Common:4; Rare:105 |