| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:210002447-210002664 | Common:5; Rare:77 | ||||
| chr2:210477547-210477699 | Rare:43 | ||||
| chr2:213284238-213284500 | Rare:85 | ||||
| chr2:215311888-215312151 | Common:8; Rare:106 | ||||
| chr2:215435658-215435973 | Common:2; Rare:74 | ||||
| chr2:215435981-215436253 | Common:2; Rare:85 | ||||
| chr2:216081762-216081925 | Common:1; Rare:57 | ||||
| chr2:216412694-216412791 | Rare:12 | ||||
| chr2:216498711-216498904 | Common:7; Rare:84 | ||||
| chr2:218217033-218217246 | Common:1; Rare:73 | ||||
| chr2:218270062-218270568 | Common:5; Rare:160; Clinvar:4; Clinvar (benign):2 | ||||
| chr2:218322953-218323275 | Common:7; Rare:104 | ||||
| chr2:218399531-218399760 | Common:1; Rare:105 | ||||
| chr2:218568307-218568702 | Common:4; Rare:98 | ||||
| chr2:218659339-218659468 | Common:2; Rare:29 |