| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:203328168-203328532 | Common:2; Rare:130 | ||||
| chr2:203495233-203495456 | Rare:37 | ||||
| chr2:203533380-203533549 | Rare:31 | ||||
| chr2:203535155-203535546 | Common:3; Rare:150 | ||||
| chr2:205682351-205682578 | Rare:41 | ||||
| chr2:206085767-206086060 | Common:2; Rare:78 | ||||
| chr2:206086078-206086188 | Rare:14 | ||||
| chr2:206086277-206086303 | Rare:3 | ||||
| chr2:206159198-206159327 | Common:1; Rare:35; Clinvar (benign):1 | ||||
| chr2:206159362-206160058 | Common:4; Rare:211; Clinvar (benign):1 | ||||
| chr2:206274505-206274736 | Rare:65 | ||||
| chr2:206274916-206275065 | Common:1; Rare:53 | ||||
| chr2:206765249-206765654 | Common:3; Rare:121; Clinvar:4; Clinvar (benign):5 | ||||
| chr2:207165928-207166094 | Rare:30 | ||||
| chr2:207529808-207530111 | Common:1; Rare:82 |