| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:42169151-42169446 | Common:1; Rare:143 | ||||
| chr2:43595917-43596222 | Common:1; Rare:107 | ||||
| chr2:43995959-43996335 | Common:4; Rare:159; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:44361480-44361590 | Common:1; Rare:36 | ||||
| chr2:44361760-44362007 | Common:1; Rare:76 | ||||
| chr2:46335858-46335900 | Rare:5 | ||||
| chr2:46541532-46541817 | Rare:64 | ||||
| chr2:46616982-46617257 | Common:6; Rare:118 | ||||
| chr2:46915726-46915908 | Common:1; Rare:55; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:47176446-47176606 | Rare:111; Clinvar (benign):5 | ||||
| chr2:47402945-47403192 | Common:1; Rare:114; Clinvar:37; Clinvar (benign):26 | ||||
| chr2:47782809-47783202 | Common:3; Rare:162; Clinvar:4; Clinvar (benign):8 | ||||
| chr2:47905495-47905819 | Common:3; Rare:155 | ||||
| chr2:48440609-48440815 | Common:6; Rare:86 | ||||
| chr2:53767735-53767913 | Common:2; Rare:75 |