| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:230863539-230863704 | Rare:25 | ||||
| chr1:231039361-231039453 | Common:1; Rare:30 | ||||
| chr1:231395353-231395740 | Common:6; Rare:70 | ||||
| chr1:231395861-231395940 | Common:1; Rare:11 | ||||
| chr1:231421268-231421371 | Rare:38; Clinvar:2; Clinvar (benign):1 | ||||
| chr1:231421612-231421919 | Common:1; Rare:102; Clinvar:5; Clinvar (benign):3 | ||||
| chr1:231422095-231422352 | Common:2; Rare:102; Clinvar:3; Clinvar (benign):3 | ||||
| chr1:231422401-231422765 | Common:5; Rare:127; Clinvar:5; Clinvar (benign):5 | ||||
| chr1:231493579-231493748 | Rare:29 | ||||
| chr1:231493887-231494057 | Rare:37 | ||||
| chr1:231600450-231600642 | Common:2; Rare:32 | ||||
| chr1:231603886-231603943 | Rare:7 | ||||
| chr1:231900090-231900257 | Rare:21 | ||||
| chr1:231929500-231929616 | Rare:31 | ||||
| chr1:231934897-231935037 | Rare:25 |