| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:206085772-206085960 | Common:1; Rare:54 | ||||
| chr2:206159367-206160075 | Common:4; Rare:216; Clinvar (benign):1 | ||||
| chr2:206213353-206213544 | Rare:28 | ||||
| chr2:206274921-206275041 | Rare:44 | ||||
| chr2:206765273-206765654 | Common:3; Rare:108; Clinvar:4; Clinvar (benign):5 | ||||
| chr2:207165928-207166094 | Rare:30 | ||||
| chr2:207529734-207530104 | Common:3; Rare:110 | ||||
| chr2:208254231-208254369 | Rare:32 | ||||
| chr2:208254991-208255238 | Common:2; Rare:64 | ||||
| chr2:208266074-208266302 | Common:7; Rare:76; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:210477573-210477690 | Rare:39 | ||||
| chr2:213284203-213284493 | Rare:96 | ||||
| chr2:215311859-215312133 | Common:8; Rare:105 | ||||
| chr2:215409534-215410117 | Rare:161 | ||||
| chr2:215435632-215436160 | Common:3; Rare:132 |