| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:1324600-1324822 | Common:3; Rare:124 | ||||
| chr1:1375284-1375545 | Common:5; Rare:70 | ||||
| chr1:1658947-1659039 | Common:1; Rare:34 | ||||
| chr1:1724325-1724449 | Common:3; Rare:43 | ||||
| chr1:2391540-2391868 | Common:2; Rare:120 | ||||
| chr1:2556294-2556399 | Common:1; Rare:46 | ||||
| chr1:3900219-3900398 | Common:11; Rare:85 | ||||
| chr1:7954247-7954290 | Rare:8 | ||||
| chr1:8878611-8878835 | Rare:113 | ||||
| chr1:9687517-9687684 | Common:1; Rare:41 | ||||
| chr1:9943292-9943488 | Common:2; Rare:46 | ||||
| chr1:11262505-11262850 | Common:2; Rare:100 | ||||
| chr1:13749154-13749438 | Common:2; Rare:96 | ||||
| chr1:15526553-15526880 | Common:2; Rare:100 | ||||
| chr1:17054021-17054266 | Common:1; Rare:73; Clinvar:1; Clinvar (benign):3 |