| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:218034746-218035125 | Common:3; Rare:86 | ||||
| chr2:218216922-218217287 | Common:3; Rare:111 | ||||
| chr2:218217621-218217850 | Common:1; Rare:47 | ||||
| chr2:218270073-218270593 | Common:5; Rare:168; Clinvar:5; Clinvar (benign):2 | ||||
| chr2:218286554-218286653 | Common:1; Rare:11 | ||||
| chr2:218286724-218287014 | Common:1; Rare:51 | ||||
| chr2:218287210-218287417 | Common:1; Rare:36 | ||||
| chr2:218292471-218292645 | Common:1; Rare:51 | ||||
| chr2:218322971-218323310 | Common:7; Rare:111 | ||||
| chr2:218397930-218398284 | Common:2; Rare:115 | ||||
| chr2:218398490-218398553 | Common:1; Rare:23 | ||||
| chr2:218399442-218399936 | Common:1; Rare:217 | ||||
| chr2:218400923-218401014 | Common:6; Rare:37 | ||||
| chr2:218568046-218568124 | Rare:18 | ||||
| chr2:218568181-218568641 | Common:5; Rare:122 |