| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:23368130-23368620 | Common:3; Rare:257 | ||||
| chr1:23368829-23368997 | Common:2; Rare:108 | ||||
| chr1:23424629-23424869 | Common:2; Rare:141 | ||||
| chr1:23484125-23484485 | Common:5; Rare:169 | ||||
| chr1:23484570-23484880 | Common:8; Rare:93 | ||||
| chr1:23531184-23531492 | Common:4; Rare:76 | ||||
| chr1:23559329-23559762 | Common:4; Rare:309 | ||||
| chr1:23691707-23691853 | Common:6; Rare:105; Clinvar:4; Clinvar (benign):3 | ||||
| chr1:23743302-23743509 | Rare:135 | ||||
| chr1:23778224-23778461 | Common:12; Rare:222 | ||||
| chr1:23791066-23791247 | Rare:101 | ||||
| chr1:23799374-23799798 | Common:2; Rare:145 | ||||
| chr1:23800702-23800984 | Common:1; Rare:100 | ||||
| chr1:23825389-23825541 | Common:4; Rare:89; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr1:23868280-23868441 | Common:4; Rare:50; Clinvar:1; Clinvar (benign):3 |