| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:207321291-207321544 | Common:3; Rare:65 | ||||
| chr1:207321545-207321718 | Rare:45 | ||||
| chr1:207454185-207454364 | Common:2; Rare:37; Clinvar:1 | ||||
| chr1:207751831-207752141 | Common:2; Rare:100 | ||||
| chr1:207890309-207890459 | Rare:40 | ||||
| chr1:209651190-209651570 | Common:4; Rare:68 | ||||
| chr1:209652313-209653068 | Common:6; Rare:185; Clinvar:2; Clinvar (benign):1 | ||||
| chr1:209784478-209784855 | Common:3; Rare:118 | ||||
| chr1:209806089-209806375 | Common:5; Rare:98; Clinvar:2; Clinvar (benign):2 | ||||
| chr1:209827802-209828064 | Common:2; Rare:66 | ||||
| chr1:210232510-210232980 | Common:3; Rare:108 | ||||
| chr1:210327981-210328233 | Common:3; Rare:35 | ||||
| chr1:210328801-210328920 | Common:1; Rare:47 | ||||
| chr1:210329216-210329438 | Common:1; Rare:65 | ||||
| chr1:211258361-211258505 | Rare:32 |