| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:235883671-235883888 | Rare:40 | ||||
| chr1:236142006-236142068 | Rare:20 | ||||
| chr1:236142344-236142598 | Common:4; Rare:60 | ||||
| chr1:236281864-236282295 | Common:7; Rare:124 | ||||
| chr1:236523804-236524092 | Common:3; Rare:85 | ||||
| chr1:236524487-236524675 | Common:1; Rare:50 | ||||
| chr1:236604466-236604886 | Common:5; Rare:116 | ||||
| chr1:236686392-236686541 | Rare:61 | ||||
| chr1:236795023-236795547 | Common:7; Rare:206; Clinvar:6; Clinvar (benign):1 | ||||
| chr1:236795580-236795720 | Common:1; Rare:68; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr1:236795724-236795914 | Common:1; Rare:66; Clinvar:1; Clinvar (benign):1 | ||||
| chr1:241519145-241519301 | Rare:27 | ||||
| chr1:241519635-241520036 | Common:3; Rare:121; Clinvar:13; Clinvar (benign):12; Clinvar (pathogenic):4 | ||||
| chr1:241532074-241532270 | Common:1; Rare:40 | ||||
| chr1:241639720-241639912 | Common:2; Rare:47 |