| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:32063347-32063694 | Common:1; Rare:121; Clinvar:1 | ||||
| chr2:32165665-32165898 | Common:1; Rare:92 | ||||
| chr2:32277814-32277981 | Common:1; Rare:42 | ||||
| chr2:32627954-32628127 | Rare:55 | ||||
| chr2:33599208-33599356 | Rare:64 | ||||
| chr2:37084269-37084561 | Common:4; Rare:110 | ||||
| chr2:37231559-37231703 | Common:4; Rare:79; Clinvar (benign):3 | ||||
| chr2:37671624-37671947 | Common:12; Rare:114 | ||||
| chr2:38377243-38377495 | Common:2; Rare:101 | ||||
| chr2:38602880-38603180 | Common:4; Rare:119 | ||||
| chr2:38751348-38751625 | Common:4; Rare:126 | ||||
| chr2:38875902-38876055 | Common:1; Rare:54 | ||||
| chr2:39437087-39437453 | Common:4; Rare:130 | ||||
| chr2:42169151-42169440 | Common:1; Rare:140 | ||||
| chr2:43595986-43596205 | Common:1; Rare:75 |