| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:113627021-113627304 | Common:3; Rare:87 | ||||
| chr2:113756513-113756755 | Common:3; Rare:76 | ||||
| chr2:113889709-113890224 | Common:8; Rare:162 | ||||
| chr2:113890226-113890285 | Common:1; Rare:23 | ||||
| chr2:113890295-113890322 | Rare:4 | ||||
| chr2:118014017-118014254 | Common:2; Rare:125 | ||||
| chr2:118088344-118088516 | Common:1; Rare:53 | ||||
| chr2:119366742-119367060 | Common:1; Rare:94 | ||||
| chr2:119431567-119431866 | Common:9; Rare:70 | ||||
| chr2:119679086-119679222 | Common:3; Rare:44 | ||||
| chr2:119759741-119759831 | Common:1; Rare:19 | ||||
| chr2:120252608-120252964 | Common:3; Rare:117 | ||||
| chr2:121530579-121530889 | Common:7; Rare:132; Clinvar (pathogenic):1 | ||||
| chr2:121649394-121649809 | Common:2; Rare:122 | ||||
| chr2:121649979-121650138 | Rare:46 |