| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:212699946-212700090 | Common:2; Rare:33 | ||||
| chr1:212791401-212791574 | Rare:54 | ||||
| chr1:212791656-212791994 | Common:6; Rare:158 | ||||
| chr1:212792269-212792341 | Rare:8 | ||||
| chr1:212857693-212857887 | Common:1; Rare:38 | ||||
| chr1:212858045-212858405 | Common:6; Rare:92; Clinvar:3; Clinvar (benign):1 | ||||
| chr1:212950371-212950610 | Common:2; Rare:57 | ||||
| chr1:213015184-213015317 | Rare:31 | ||||
| chr1:213015393-213015647 | Rare:69 | ||||
| chr1:213015673-213015949 | Rare:85 | ||||
| chr1:213051134-213051394 | Common:2; Rare:89 | ||||
| chr1:214280942-214281038 | Rare:31 | ||||
| chr1:214281156-214281298 | Common:1; Rare:46 | ||||
| chr1:214281368-214281576 | Common:2; Rare:100 | ||||
| chr1:214551207-214551382 | Common:2; Rare:63 |