| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:203626525-203626858 | Common:1; Rare:77 | ||||
| chr1:203627050-203627116 | Rare:17 | ||||
| chr1:204411354-204411424 | Rare:26; Clinvar:1 | ||||
| chr1:204411738-204412141 | Common:11; Rare:127 | ||||
| chr1:204516288-204516489 | Common:1; Rare:61 | ||||
| chr1:205229485-205229708 | Common:10; Rare:48 | ||||
| chr1:205813148-205813442 | Common:3; Rare:123 | ||||
| chr1:205813756-205813823 | Rare:18 | ||||
| chr1:207032642-207032936 | Common:3; Rare:50 | ||||
| chr1:207052973-207053300 | Common:1; Rare:85 | ||||
| chr1:207321710-207321783 | Rare:18 | ||||
| chr1:207751856-207752293 | Common:2; Rare:146; Clinvar:1 | ||||
| chr1:209652369-209652612 | Common:3; Rare:54; Clinvar:2; Clinvar (benign):1 | ||||
| chr1:209675264-209675476 | Common:1; Rare:52 | ||||
| chr1:209686050-209686217 | Rare:25 |