| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:8422967-8423069 | Rare:27 | ||||
| chr1:8423595-8423918 | Common:1; Rare:130 | ||||
| chr1:8424075-8424494 | Common:3; Rare:103 | ||||
| chr1:8703177-8703486 | Common:1; Rare:101 | ||||
| chr1:8878578-8878872 | Rare:155 | ||||
| chr1:9943251-9943500 | Common:3; Rare:67 | ||||
| chr1:10032756-10033077 | Common:2; Rare:82 | ||||
| chr1:10398868-10399097 | Common:2; Rare:86 | ||||
| chr1:11262493-11262817 | Common:2; Rare:98 | ||||
| chr1:11273328-11273503 | Common:2; Rare:36; Clinvar:1; Clinvar (benign):2 | ||||
| chr1:11654401-11654501 | Rare:28 | ||||
| chr1:11654821-11654914 | Common:2; Rare:26 | ||||
| chr1:11735810-11736211 | Common:3; Rare:109 | ||||
| chr1:11805896-11806265 | Common:2; Rare:102; Clinvar:1 | ||||
| chr1:11934485-11934784 | Common:6; Rare:98; Clinvar:6; Clinvar (benign):1 |