| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:233655707-233656600 | Common:8; Rare:247 | ||||
| chr1:234373150-234373850 | Common:10; Rare:1454; Clinvar (benign):51 | ||||
| chr1:234373891-234374347 | Common:5; Rare:171; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr1:234478652-234478814 | Common:2; Rare:67 | ||||
| chr1:234478870-234479251 | Common:12; Rare:240 | ||||
| chr1:234606976-234607664 | Common:2; Rare:236; Clinvar (benign):1 | ||||
| chr1:234608010-234609553 | Common:33; Rare:1821; Clinvar (benign):9 | ||||
| chr1:234609491-234609836 | Common:2; Rare:183 | ||||
| chr1:234609820-234610030 | Rare:119 | ||||
| chr1:235128126-235128593 | Common:8; Rare:292 | ||||
| chr1:235128685-235129400 | Common:4; Rare:771 | ||||
| chr1:235160520-235160920 | Common:4; Rare:170 | ||||
| chr1:235160900-235161751 | Common:12; Rare:1315 | ||||
| chr1:235326590-235327930 | Common:13; Rare:1072 | ||||
| chr1:235327933-235329137 | Common:40; Rare:1926 |