| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:180154703-180155052 | Common:4; Rare:124 | ||||
| chr1:180502291-180502647 | Common:1; Rare:122 | ||||
| chr1:181088494-181088739 | Common:1; Rare:93 | ||||
| chr1:182389868-182390116 | Rare:41 | ||||
| chr1:182390378-182390468 | Common:1; Rare:24 | ||||
| chr1:182391282-182391510 | Common:1; Rare:49 | ||||
| chr1:182391540-182391606 | Rare:26 | ||||
| chr1:182391677-182392068 | Common:5; Rare:144; Clinvar:6; Clinvar (benign):5 | ||||
| chr1:182789610-182789805 | Common:2; Rare:70 | ||||
| chr1:182839194-182839428 | Common:1; Rare:99 | ||||
| chr1:183023075-183023292 | Common:4; Rare:52 | ||||
| chr1:183186091-183186382 | Common:5; Rare:73; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr1:183472255-183472544 | Common:2; Rare:99 | ||||
| chr1:183563193-183563562 | Common:4; Rare:94; Clinvar:6; Clinvar (benign):4 | ||||
| chr1:183590886-183591063 | Common:3; Rare:33 |