| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:37248925-37249148 | Common:3; Rare:88 | ||||
| chr5:37249212-37249519 | Common:2; Rare:180; Clinvar:2; Clinvar (benign):3 | ||||
| chr5:37249470-37249747 | Common:1; Rare:74 | ||||
| chr5:37370790-37370970 | Common:2; Rare:110 | ||||
| chr5:37370985-37371153 | Rare:128 | ||||
| chr5:37379155-37379504 | Common:2; Rare:147 | ||||
| chr5:38556361-38556898 | Common:5; Rare:292 | ||||
| chr5:38557351-38557770 | Common:3; Rare:124 | ||||
| chr5:38845596-38846205 | Common:5; Rare:256 | ||||
| chr5:39073800-39074162 | Common:11; Rare:176 | ||||
| chr5:39074324-39074579 | Common:2; Rare:196 | ||||
| chr5:39424764-39425308 | Common:6; Rare:238 | ||||
| chr5:40679183-40679450 | Common:4; Rare:83 | ||||
| chr5:40679665-40679946 | Common:3; Rare:118 | ||||
| chr5:40755737-40756114 | Common:1; Rare:129 |