| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:180229775-180230175 | Common:9; Rare:193 | ||||
| chr1:180502160-180502779 | Common:8; Rare:930 | ||||
| chr1:180502770-180503090 | Rare:452 | ||||
| chr1:180631752-180632880 | Common:25; Rare:997 | ||||
| chr1:181022129-181023301 | Common:85; Rare:980 | ||||
| chr1:181032980-181033500 | Common:5; Rare:144 | ||||
| chr1:181033625-181034198 | Common:2; Rare:186 | ||||
| chr1:181034203-181034394 | Common:4; Rare:40 | ||||
| chr1:181088091-181088956 | Common:11; Rare:1074 | ||||
| chr1:182385095-182385495 | Common:1; Rare:93 | ||||
| chr1:182388328-182388890 | Common:3; Rare:159 | ||||
| chr1:182389150-182389922 | Common:6; Rare:186 | ||||
| chr1:182390069-182390469 | Common:4; Rare:95 | ||||
| chr1:182390472-182390913 | Common:8; Rare:240; Clinvar:22; Clinvar (benign):6 | ||||
| chr1:182391020-182391700 | Common:7; Rare:522 |