| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:213015567-213015596 | Rare:4 | ||||
| chr2:213151496-213152042 | Common:3; Rare:198 | ||||
| chr2:213152187-213152315 | Common:2; Rare:28 | ||||
| chr2:213152329-213152348 | Rare:3 | ||||
| chr2:213152539-213152592 | Common:1; Rare:9 | ||||
| chr2:213284147-213284514 | Rare:117 | ||||
| chr2:214809011-214809202 | Common:4; Rare:42 | ||||
| chr2:214809213-214809447 | Common:2; Rare:71; Clinvar:7; Clinvar (benign):6 | ||||
| chr2:214809568-214809721 | Common:4; Rare:64; Clinvar:3; Clinvar (benign):5 | ||||
| chr2:214809844-214810309 | Common:10; Rare:139 | ||||
| chr2:215311846-215312198 | Common:8; Rare:136 | ||||
| chr2:216013235-216013415 | Common:1; Rare:65 | ||||
| chr2:216033555-216033685 | Rare:27 | ||||
| chr2:216057674-216058169 | Common:1; Rare:84 | ||||
| chr2:216081720-216081940 | Common:1; Rare:75 |