| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:109613841-109613986 | Common:1; Rare:56 | ||||
| chr2:110204941-110205064 | Common:1; Rare:55; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:111122431-111122744 | Common:3; Rare:130 | ||||
| chr2:111884142-111884255 | Rare:33 | ||||
| chr2:112275404-112275637 | Common:1; Rare:76 | ||||
| chr2:112584410-112584645 | Common:1; Rare:67 | ||||
| chr2:112584772-112584854 | Rare:20 | ||||
| chr2:112645707-112645968 | Common:1; Rare:101 | ||||
| chr2:113627054-113627250 | Common:1; Rare:55 | ||||
| chr2:113756514-113756791 | Common:4; Rare:94 | ||||
| chr2:113889710-113890290 | Common:9; Rare:186 | ||||
| chr2:118014056-118014221 | Common:2; Rare:93 | ||||
| chr2:118088329-118088509 | Common:1; Rare:53 | ||||
| chr2:119223544-119223845 | Common:1; Rare:84 | ||||
| chr2:119366788-119367076 | Common:1; Rare:91 |