| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:112645566-112645968 | Common:2; Rare:137 | ||||
| chr2:113117571-113117912 | Common:2; Rare:73 | ||||
| chr2:113437717-113437862 | Common:1; Rare:64 | ||||
| chr2:113627004-113627272 | Common:1; Rare:80 | ||||
| chr2:113756532-113756799 | Common:3; Rare:92 | ||||
| chr2:113889765-113890290 | Common:9; Rare:164 | ||||
| chr2:113890923-113891187 | Rare:56 | ||||
| chr2:117814623-117814783 | Common:1; Rare:64 | ||||
| chr2:118014041-118014243 | Common:2; Rare:108 | ||||
| chr2:118088165-118088650 | Common:2; Rare:121 | ||||
| chr2:119366770-119367054 | Common:1; Rare:86 | ||||
| chr2:119679072-119679222 | Common:3; Rare:48 | ||||
| chr2:120012949-120013084 | Common:2; Rare:55 | ||||
| chr2:121530579-121530906 | Common:7; Rare:156; Clinvar (pathogenic):3 | ||||
| chr2:121649418-121649650 | Common:2; Rare:67 |