| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:208255063-208255231 | Common:2; Rare:45 | ||||
| chr2:210477572-210477690 | Rare:39 | ||||
| chr2:215312024-215312124 | Common:6; Rare:47 | ||||
| chr2:215435632-215435767 | Common:2; Rare:36 | ||||
| chr2:215435847-215435962 | Rare:19 | ||||
| chr2:215435973-215436405 | Common:2; Rare:125 | ||||
| chr2:216081765-216081906 | Common:1; Rare:46 | ||||
| chr2:216498754-216498872 | Common:1; Rare:49 | ||||
| chr2:218270104-218270532 | Common:5; Rare:130; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:218659339-218659781 | Common:4; Rare:112 | ||||
| chr2:218671963-218672037 | Rare:27 | ||||
| chr2:219229565-219229838 | Common:2; Rare:76 | ||||
| chr2:219245414-219245531 | Rare:33 | ||||
| chr2:219498705-219498929 | Common:2; Rare:47 | ||||
| chr2:224039282-224039402 | Rare:45 |