| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:162069423-162069733 | Common:1; Rare:75 | ||||
| chr1:162497717-162497961 | Common:3; Rare:78 | ||||
| chr1:162498012-162498209 | Rare:84 | ||||
| chr1:162561340-162561634 | Common:3; Rare:110 | ||||
| chr1:162631651-162631722 | Rare:12 | ||||
| chr1:162632259-162632599 | Rare:66 | ||||
| chr1:162767057-162767360 | Common:3; Rare:67; Clinvar (benign):1 | ||||
| chr1:162790549-162790815 | Common:4; Rare:78 | ||||
| chr1:162855440-162855658 | Common:1; Rare:40 | ||||
| chr1:162855760-162855978 | Rare:47 | ||||
| chr1:163070891-163070937 | Rare:7 | ||||
| chr1:163071804-163072106 | Common:4; Rare:61 | ||||
| chr1:163202812-163203261 | Common:1; Rare:87 | ||||
| chr1:163321694-163322234 | Common:1; Rare:138 | ||||
| chr1:164558850-164559229 | Common:1; Rare:94 |