| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:43595924-43596203 | Common:1; Rare:97 | ||||
| chr2:43995960-43996299 | Common:4; Rare:145; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:44361473-44362007 | Common:3; Rare:168 | ||||
| chr2:46297249-46297437 | Common:3; Rare:66 | ||||
| chr2:46297664-46297796 | Rare:45; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:46375412-46375775 | Common:2; Rare:94 | ||||
| chr2:46381419-46381720 | Common:1; Rare:92 | ||||
| chr2:46616972-46617261 | Common:6; Rare:124 | ||||
| chr2:46698944-46699340 | Common:1; Rare:120 | ||||
| chr2:46915722-46915939 | Common:2; Rare:71; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:46916044-46916175 | Common:2; Rare:43 | ||||
| chr2:46941648-46941785 | Common:2; Rare:53; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:47176430-47176680 | Common:2; Rare:143; Clinvar (benign):5 | ||||
| chr2:47402945-47403197 | Common:1; Rare:117; Clinvar:39; Clinvar (benign):27 | ||||
| chr2:48440619-48440865 | Common:8; Rare:115 |