| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:157138334-157138766 | Common:6; Rare:138 | ||||
| chr1:157993510-157993679 | Common:2; Rare:51 | ||||
| chr1:159780726-159781026 | Common:5; Rare:70 | ||||
| chr1:159829300-159829620 | Common:3; Rare:69 | ||||
| chr1:159854744-159855049 | Common:1; Rare:99 | ||||
| chr1:159900151-159900300 | Rare:35 | ||||
| chr1:159925463-159925656 | Common:1; Rare:53 | ||||
| chr1:159945598-159945831 | Common:2; Rare:58 | ||||
| chr1:160031834-160032086 | Common:2; Rare:67 | ||||
| chr1:160098505-160099153 | Common:6; Rare:181 | ||||
| chr1:160193050-160193460 | Common:6; Rare:79 | ||||
| chr1:160205237-160205461 | Common:2; Rare:63 | ||||
| chr1:160262369-160262702 | Common:1; Rare:97 | ||||
| chr1:160285066-160285264 | Common:3; Rare:73; Clinvar:2; Clinvar (benign):4 | ||||
| chr1:160343179-160343399 | Rare:90 |