| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:112584378-112584645 | Common:1; Rare:74 | ||||
| chr2:112645707-112645954 | Common:1; Rare:93 | ||||
| chr2:112646261-112646393 | Common:1; Rare:49 | ||||
| chr2:112764578-112764861 | Common:2; Rare:94; Clinvar (pathogenic):1 | ||||
| chr2:113173851-113174007 | Common:2; Rare:29 | ||||
| chr2:113437634-113437874 | Common:2; Rare:91 | ||||
| chr2:113627070-113627272 | Common:1; Rare:57 | ||||
| chr2:113756604-113756792 | Common:3; Rare:73 | ||||
| chr2:113889709-113890165 | Common:8; Rare:152 | ||||
| chr2:118014037-118014249 | Common:2; Rare:115 | ||||
| chr2:118088293-118088509 | Common:1; Rare:63 | ||||
| chr2:119366731-119367054 | Common:1; Rare:93 | ||||
| chr2:119679090-119679236 | Common:4; Rare:47 | ||||
| chr2:120012973-120013084 | Common:1; Rare:44 | ||||
| chr2:120223029-120223191 | Common:5; Rare:40 |