| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:236281871-236282249 | Common:7; Rare:113 | ||||
| chr1:236395216-236395522 | Rare:72 | ||||
| chr1:236523378-236523383 | |||||
| chr1:236523867-236524060 | Common:2; Rare:49 | ||||
| chr1:236541581-236541678 | Common:10; Rare:22 | ||||
| chr1:236604450-236604626 | Common:4; Rare:57 | ||||
| chr1:236795086-236795566 | Common:7; Rare:202; Clinvar:6; Clinvar (benign):2 | ||||
| chr1:236795734-236795863 | Common:1; Rare:44; Clinvar:1; Clinvar (benign):1 | ||||
| chr1:239719046-239719174 | Common:1; Rare:18 | ||||
| chr1:241519637-241519977 | Common:3; Rare:109; Clinvar:13; Clinvar (benign):12; Clinvar (pathogenic):4 | ||||
| chr1:241848114-241848255 | Common:1; Rare:25 | ||||
| chr1:241998673-241998849 | Rare:55 | ||||
| chr1:243254629-243254949 | Common:2; Rare:97 | ||||
| chr1:243255047-243255497 | Common:1; Rare:102 | ||||
| chr1:243255729-243256157 | Common:1; Rare:123; Clinvar:4; Clinvar (benign):1 |