| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:23926672-23926758 | Common:2; Rare:33 | ||||
| chr2:23927026-23927334 | Common:3; Rare:106 | ||||
| chr2:23940363-23940537 | Common:3; Rare:63 | ||||
| chr2:24076205-24076882 | Common:2; Rare:148 | ||||
| chr2:24084271-24084479 | Common:6; Rare:88 | ||||
| chr2:24123279-24123506 | Common:1; Rare:60 | ||||
| chr2:24360310-24360574 | Common:3; Rare:72 | ||||
| chr2:24793067-24793175 | Rare:53 | ||||
| chr2:24971675-24972153 | Common:3; Rare:169 | ||||
| chr2:25878485-25878787 | Common:5; Rare:94 | ||||
| chr2:26033764-26034179 | Common:4; Rare:155 | ||||
| chr2:26034320-26034745 | Common:3; Rare:104 | ||||
| chr2:26244573-26244984 | Common:2; Rare:152; Clinvar:6; Clinvar (benign):9 | ||||
| chr2:26345798-26346205 | Common:1; Rare:122 | ||||
| chr2:26764193-26764421 | Common:3; Rare:76 |