| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:27628976-27629102 | Common:1; Rare:71 | ||||
| chr2:27663361-27663934 | Rare:187 | ||||
| chr2:27890348-27890809 | Common:1; Rare:127 | ||||
| chr2:29115416-29115636 | Common:1; Rare:59 | ||||
| chr2:31233970-31234256 | Rare:71 | ||||
| chr2:32039752-32039877 | Rare:39 | ||||
| chr2:32165745-32165895 | Common:1; Rare:54 | ||||
| chr2:32627934-32628117 | Rare:55 | ||||
| chr2:36355492-36355948 | Common:2; Rare:165 | ||||
| chr2:36356256-36356612 | Common:2; Rare:142 | ||||
| chr2:37084312-37084544 | Common:3; Rare:83 | ||||
| chr2:37231553-37231734 | Common:4; Rare:105; Clinvar:1; Clinvar (benign):4 | ||||
| chr2:37671588-37671827 | Common:11; Rare:108 | ||||
| chr2:38076137-38076282 | Rare:36 | ||||
| chr2:38875916-38876067 | Rare:51 |