| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:118088319-118088540 | Common:1; Rare:62 | ||||
| chr2:119366770-119367060 | Common:1; Rare:88 | ||||
| chr2:119544389-119544546 | Rare:66 | ||||
| chr2:119678943-119679248 | Common:6; Rare:79 | ||||
| chr2:119759741-119759849 | Common:1; Rare:26 | ||||
| chr2:120012813-120013190 | Common:3; Rare:147 | ||||
| chr2:120252630-120252955 | Common:3; Rare:108 | ||||
| chr2:121530340-121530901 | Common:10; Rare:217; Clinvar (pathogenic):3 | ||||
| chr2:121649141-121649144 | |||||
| chr2:121649385-121649711 | Common:3; Rare:96 | ||||
| chr2:121649957-121650166 | Rare:57 | ||||
| chr2:121736703-121737124 | Common:5; Rare:173 | ||||
| chr2:121755421-121755821 | Common:5; Rare:132 | ||||
| chr2:124024719-124025588 | Common:7; Rare:206 | ||||
| chr2:127106920-127107366 | Common:5; Rare:135; Clinvar:9; Clinvar (benign):3 |