| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:215375212-215375589 | Common:1; Rare:92 | ||||
| chr2:215409534-215410115 | Rare:161 | ||||
| chr2:215435653-215435948 | Common:2; Rare:67 | ||||
| chr2:215435950-215436395 | Common:2; Rare:132 | ||||
| chr2:216081722-216081919 | Common:1; Rare:66 | ||||
| chr2:216412272-216412553 | Common:3; Rare:66; Clinvar (benign):2 | ||||
| chr2:216498774-216498894 | Common:4; Rare:57 | ||||
| chr2:216694723-216694803 | Rare:24 | ||||
| chr2:217978849-217978913 | Common:1; Rare:21 | ||||
| chr2:218216892-218217246 | Common:2; Rare:112 | ||||
| chr2:218270062-218270541 | Common:5; Rare:151; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:218279036-218279356 | Common:2; Rare:93 | ||||
| chr2:218292470-218292644 | Common:1; Rare:52 | ||||
| chr2:218322988-218323429 | Common:6; Rare:155; Clinvar:1 | ||||
| chr2:218381920-218382251 | Common:2; Rare:63 |