| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:95233945-95234260 | Common:5; Rare:99 | ||||
| chr1:96721579-96721861 | Common:2; Rare:136 | ||||
| chr1:97920894-97921150 | Rare:102; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr1:98661581-98661879 | Common:2; Rare:105 | ||||
| chr1:99264184-99264587 | Common:2; Rare:119 | ||||
| chr1:99849975-99850400 | Common:1; Rare:117; Clinvar:2 | ||||
| chr1:99968987-99969311 | Common:2; Rare:46 | ||||
| chr1:99969823-99970078 | Rare:55 | ||||
| chr1:100037973-100038143 | Common:1; Rare:69 | ||||
| chr1:100132839-100133243 | Common:3; Rare:159 | ||||
| chr1:100249796-100249977 | Common:2; Rare:68; Clinvar:1; Clinvar (benign):1 | ||||
| chr1:100266107-100266419 | Common:4; Rare:111 | ||||
| chr1:100351195-100351415 | Common:1; Rare:53 | ||||
| chr1:100351612-100351728 | Common:1; Rare:38 | ||||
| chr1:100894639-100894954 | Common:2; Rare:75 |