| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:44127278-44127663 | Common:4; Rare:107 | ||||
| chr6:44223489-44223620 | Common:1; Rare:46 | ||||
| chr6:44387439-44387801 | Common:4; Rare:99 | ||||
| chr6:45377845-45378149 | Common:2; Rare:103 | ||||
| chr6:46652718-46653022 | Rare:75 | ||||
| chr6:47477714-47478238 | Common:5; Rare:150; Clinvar:6; Clinvar (benign):7 | ||||
| chr6:49463264-49463412 | Rare:42 | ||||
| chr6:52284756-52285094 | Common:2; Rare:99 | ||||
| chr6:52995267-52995825 | Common:4; Rare:229 | ||||
| chr6:53065253-53065598 | Common:1; Rare:116 | ||||
| chr6:53348878-53349213 | Common:2; Rare:128 | ||||
| chr6:54846623-54846762 | Common:1; Rare:36 | ||||
| chr6:56542728-56542954 | Common:1; Rare:41 | ||||
| chr6:56543031-56543096 | Rare:8 | ||||
| chr6:57172515-57172798 | Common:1; Rare:88 |