| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:113812176-113812704 | Common:3; Rare:201 | ||||
| chr1:113871661-113872012 | Rare:63 | ||||
| chr1:113904543-113904673 | Common:1; Rare:45; Clinvar:1; Clinvar (benign):1 | ||||
| chr1:113904722-113905471 | Common:7; Rare:217; Clinvar (benign):2 | ||||
| chr1:113928596-113928790 | Common:2; Rare:24 | ||||
| chr1:113929216-113929660 | Common:2; Rare:137 | ||||
| chr1:113929895-113930090 | Common:1; Rare:66 | ||||
| chr1:113930217-113930262 | Rare:11 | ||||
| chr1:114510807-114511008 | Common:2; Rare:74 | ||||
| chr1:114511067-114511608 | Common:5; Rare:199 | ||||
| chr1:114581550-114581858 | Common:1; Rare:136 | ||||
| chr1:114716130-114716525 | Common:4; Rare:102; Clinvar (benign):1 | ||||
| chr1:114716704-114716848 | Rare:62; Clinvar:3 | ||||
| chr1:114757398-114757773 | Common:2; Rare:80 | ||||
| chr1:114757846-114758212 | Common:3; Rare:108 |