| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:9996958-9997358 | Common:7; Rare:245 | ||||
| chr1:10032583-10033077 | Common:14; Rare:356 | ||||
| chr1:10033098-10033588 | Common:6; Rare:153 | ||||
| chr1:10210259-10210872 | Common:21; Rare:372; Clinvar:2; Clinvar (benign):3 | ||||
| chr1:10398306-10399146 | Common:20; Rare:560 | ||||
| chr1:10399170-10399550 | Common:8; Rare:146 | ||||
| chr1:10430128-10430544 | Common:16; Rare:214 | ||||
| chr1:10430584-10430821 | Common:15; Rare:181 | ||||
| chr1:10472415-10472762 | Rare:206 | ||||
| chr1:10474787-10475030 | Rare:197; Clinvar:9; Clinvar (benign):2 | ||||
| chr1:10694371-10694593 | Rare:106 | ||||
| chr1:10694610-10695140 | Common:7; Rare:262 | ||||
| chr1:10796498-10796929 | Common:9; Rare:287 | ||||
| chr1:11012160-11012460 | Common:1; Rare:151 | ||||
| chr1:11012595-11012751 | Common:1; Rare:76; Clinvar:6; Clinvar (benign):1 |