| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:207529974-207530167 | Rare:41 | ||||
| chr2:207625250-207625613 | Common:1; Rare:103 | ||||
| chr2:210002430-210002643 | Common:3; Rare:74 | ||||
| chr2:210476697-210476871 | Rare:43 | ||||
| chr2:213284203-213284481 | Rare:90 | ||||
| chr2:215311970-215312131 | Common:7; Rare:69 | ||||
| chr2:216081773-216081925 | Common:1; Rare:55 | ||||
| chr2:216498750-216498886 | Common:3; Rare:57 | ||||
| chr2:218216936-218217287 | Common:3; Rare:111 | ||||
| chr2:218217584-218217765 | Common:1; Rare:36 | ||||
| chr2:218270106-218270490 | Common:5; Rare:118; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:218287195-218287395 | Common:1; Rare:34 | ||||
| chr2:218568307-218568592 | Common:2; Rare:74 | ||||
| chr2:218568738-218568886 | Common:1; Rare:31 | ||||
| chr2:218659577-218659755 | Common:1; Rare:44 |