| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:46915721-46916181 | Common:4; Rare:151; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:47176430-47176595 | Rare:115; Clinvar (benign):5 | ||||
| chr2:47402915-47403203 | Common:1; Rare:134; Clinvar:44; Clinvar (benign):29; Clinvar (pathogenic):1 | ||||
| chr2:47782924-47783221 | Common:2; Rare:135; Clinvar:6; Clinvar (benign):15 | ||||
| chr2:47905496-47905877 | Common:3; Rare:186 | ||||
| chr2:48314370-48314750 | Rare:139 | ||||
| chr2:48440619-48440950 | Common:8; Rare:146 | ||||
| chr2:50347529-50347665 | Common:2; Rare:42 | ||||
| chr2:50347684-50347715 | Common:1; Rare:7 | ||||
| chr2:53767559-53767871 | Common:5; Rare:109 | ||||
| chr2:53786827-53787216 | Common:1; Rare:149 | ||||
| chr2:53970766-53971278 | Common:14; Rare:180 | ||||
| chr2:54115469-54115496 | Rare:7 | ||||
| chr2:54115502-54115715 | Common:1; Rare:77 | ||||
| chr2:54330733-54330960 | Common:3; Rare:91 |