| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:40161596-40161634 | Rare:9 | ||||
| chr1:40161809-40161827 | Rare:4 | ||||
| chr1:40257658-40258307 | Common:6; Rare:167; Clinvar:9; Clinvar (benign):1 | ||||
| chr1:40315339-40315608 | Common:4; Rare:66; Clinvar (benign):1 | ||||
| chr1:40315765-40315958 | Common:1; Rare:28 | ||||
| chr1:40316087-40316265 | Common:1; Rare:47 | ||||
| chr1:40316729-40316822 | Rare:25 | ||||
| chr1:40373490-40373790 | Common:1; Rare:72 | ||||
| chr1:40374300-40374365 | Rare:7 | ||||
| chr1:40374564-40374862 | Common:13; Rare:62 | ||||
| chr1:40449849-40450415 | Common:9; Rare:186 | ||||
| chr1:40450464-40450533 | Rare:15 | ||||
| chr1:40450535-40450594 | Common:1; Rare:11 | ||||
| chr1:40450606-40450836 | Common:2; Rare:46 | ||||
| chr1:40450888-40451025 | Common:1; Rare:41 |