| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:148020673-148021153 | Common:2; Rare:121; Clinvar (benign):2 | ||||
| chr2:148021335-148021468 | Rare:29 | ||||
| chr2:148021489-148021652 | Rare:40 | ||||
| chr2:149587299-149587370 | Rare:19 | ||||
| chr2:149587685-149587882 | Common:1; Rare:57; Clinvar:1 | ||||
| chr2:150539019-150539097 | Rare:18 | ||||
| chr2:151261765-151261925 | Common:1; Rare:35 | ||||
| chr2:151289611-151289732 | Common:1; Rare:31 | ||||
| chr2:151828449-151828793 | Common:2; Rare:96 | ||||
| chr2:152175691-152176073 | Common:2; Rare:107 | ||||
| chr2:152335016-152335195 | Common:1; Rare:62 | ||||
| chr2:152717829-152718078 | Rare:97 | ||||
| chr2:152718272-152718650 | Common:2; Rare:136 | ||||
| chr2:156332673-156332904 | Rare:73; Clinvar:3 | ||||
| chr2:156333128-156333257 | Rare:27 |