| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:178451079-178451486 | Common:6; Rare:115; Clinvar:4; Clinvar (benign):3 | ||||
| chr2:178478512-178478723 | Common:1; Rare:71 | ||||
| chr2:178480205-178480489 | Common:2; Rare:81 | ||||
| chr2:179263601-179264220 | Common:10; Rare:243 | ||||
| chr2:179264265-179264415 | Common:1; Rare:38 | ||||
| chr2:179264785-179264901 | Common:2; Rare:50 | ||||
| chr2:180006813-180007421 | Common:3; Rare:153 | ||||
| chr2:180980419-180980644 | Rare:79 | ||||
| chr2:180980851-180981097 | Rare:65 | ||||
| chr2:180983904-180984155 | Rare:72 | ||||
| chr2:181457230-181457386 | Rare:59 | ||||
| chr2:182522592-182522841 | Common:2; Rare:48 | ||||
| chr2:182523036-182523434 | Rare:66 | ||||
| chr2:182715841-182716308 | Common:3; Rare:155 | ||||
| chr2:182867113-182867242 | Rare:33 |