| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:202912138-202912560 | Common:4; Rare:127 | ||||
| chr2:203014672-203014931 | Common:1; Rare:78 | ||||
| chr2:203238836-203239054 | Common:1; Rare:87 | ||||
| chr2:203239229-203239344 | Rare:40 | ||||
| chr2:203328207-203328517 | Common:2; Rare:114 | ||||
| chr2:203535246-203535581 | Common:4; Rare:146 | ||||
| chr2:205682356-205682572 | Rare:39 | ||||
| chr2:206085765-206085981 | Common:1; Rare:62 | ||||
| chr2:206086085-206086280 | Rare:25 | ||||
| chr2:206159370-206160058 | Common:4; Rare:211; Clinvar (benign):1 | ||||
| chr2:206274916-206275041 | Rare:47 | ||||
| chr2:206765273-206765654 | Common:3; Rare:108; Clinvar:4; Clinvar (benign):5 | ||||
| chr2:207165928-207166081 | Rare:28 | ||||
| chr2:207529701-207530108 | Common:3; Rare:119 | ||||
| chr2:208255047-208255228 | Common:2; Rare:48 |