| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:201451452-201451767 | Common:1; Rare:73 | ||||
| chr2:202912141-202912273 | Common:1; Rare:47 | ||||
| chr2:203328173-203328399 | Common:2; Rare:86 | ||||
| chr2:203535169-203535260 | Rare:19 | ||||
| chr2:206085765-206086058 | Common:2; Rare:77 | ||||
| chr2:206159343-206159882 | Common:4; Rare:142; Clinvar (benign):1 | ||||
| chr2:206765299-206765652 | Common:3; Rare:92; Clinvar:4; Clinvar (benign):5 | ||||
| chr2:208255019-208255238 | Common:2; Rare:58 | ||||
| chr2:208266075-208266302 | Common:7; Rare:75; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:210477527-210477716 | Rare:55 | ||||
| chr2:215436049-215436376 | Common:2; Rare:100 | ||||
| chr2:216081753-216081932 | Common:1; Rare:63 | ||||
| chr2:216498719-216498877 | Common:6; Rare:63 | ||||
| chr2:218217241-218217382 | Common:1; Rare:38 | ||||
| chr2:218270107-218270436 | Common:5; Rare:97; Clinvar (benign):1 |