| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:113759382-113759728 | Common:4; Rare:95 | ||||
| chr1:113759845-113760020 | Rare:31 | ||||
| chr1:113811801-113811948 | Rare:51 | ||||
| chr1:113812016-113812091 | Common:1; Rare:26 | ||||
| chr1:113812160-113812696 | Common:3; Rare:205 | ||||
| chr1:113904620-113904818 | Common:1; Rare:72; Clinvar (benign):2 | ||||
| chr1:113904839-113905173 | Common:3; Rare:98; Clinvar (benign):1 | ||||
| chr1:113905221-113905454 | Common:3; Rare:61 | ||||
| chr1:113905666-113905745 | Rare:29; Clinvar:2 | ||||
| chr1:113928508-113928717 | Common:3; Rare:35 | ||||
| chr1:113929051-113929159 | Rare:21 | ||||
| chr1:113929228-113929402 | Common:1; Rare:53 | ||||
| chr1:113929428-113929746 | Common:2; Rare:95 | ||||
| chr1:113929810-113930161 | Common:3; Rare:104 | ||||
| chr1:113930238-113930356 | Rare:32 |