| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:105337225-105337680 | Common:5; Rare:149 | ||||
| chr2:106194200-106194554 | Common:6; Rare:153 | ||||
| chr2:108288606-108289033 | Common:2; Rare:79 | ||||
| chr2:108449098-108449271 | Rare:68 | ||||
| chr2:108533892-108533970 | Rare:25 | ||||
| chr2:108534186-108534502 | Common:7; Rare:127 | ||||
| chr2:108719404-108719592 | Common:2; Rare:78; Clinvar (benign):2 | ||||
| chr2:109613811-109613999 | Common:1; Rare:65 | ||||
| chr2:110204961-110205106 | Rare:63; Clinvar:1 | ||||
| chr2:110677987-110678212 | Rare:75 | ||||
| chr2:111884081-111884307 | Common:2; Rare:70 | ||||
| chr2:111898305-111899092 | Common:6; Rare:190; Clinvar:1; Clinvar (benign):3 | ||||
| chr2:112255009-112255151 | Common:1; Rare:63 | ||||
| chr2:112275372-112275631 | Common:1; Rare:93 | ||||
| chr2:112542139-112542493 | Common:1; Rare:111 |