| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:158999689-159000157 | Common:6; Rare:178 | ||||
| chr1:159780701-159781125 | Common:10; Rare:185 | ||||
| chr1:159781260-159781820 | Rare:173 | ||||
| chr1:159900086-159900360 | Rare:195 | ||||
| chr1:159900400-159900910 | Rare:124 | ||||
| chr1:159923250-159923540 | Rare:63 | ||||
| chr1:159923727-159923933 | Common:1; Rare:36 | ||||
| chr1:159924454-159924820 | Rare:202 | ||||
| chr1:159925140-159925370 | Common:4; Rare:36 | ||||
| chr1:159925361-159925636 | Common:2; Rare:111 | ||||
| chr1:159945537-159945790 | Common:4; Rare:118 | ||||
| chr1:159945732-159945844 | Common:1; Rare:26 | ||||
| chr1:159945892-159946332 | Common:2; Rare:182 | ||||
| chr1:160031723-160032301 | Common:8; Rare:290; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr1:160098399-160099180 | Common:8; Rare:194 |