| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:202871680-202872010 | Common:1; Rare:90 | ||||
| chr2:202911606-202911730 | Rare:23 | ||||
| chr2:202911881-202912295 | Common:2; Rare:113 | ||||
| chr2:203014483-203014940 | Common:1; Rare:145 | ||||
| chr2:203083792-203084192 | Common:7; Rare:65 | ||||
| chr2:203238760-203239070 | Common:3; Rare:115 | ||||
| chr2:203239179-203239373 | Rare:65 | ||||
| chr2:203327952-203328394 | Common:2; Rare:148 | ||||
| chr2:203535204-203535483 | Common:3; Rare:106 | ||||
| chr2:203535774-203535877 | Common:1; Rare:21 | ||||
| chr2:204545210-204545540 | Common:2; Rare:80 | ||||
| chr2:205682346-205682503 | Rare:28 | ||||
| chr2:205763811-205764211 | Common:1; Rare:129 | ||||
| chr2:206086132-206086296 | Rare:16 | ||||
| chr2:206159344-206159686 | Common:3; Rare:105; Clinvar (benign):1 |