| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:144095524-144095831 | Common:6; Rare:90 | ||||
| chr6:144150247-144150537 | Common:5; Rare:84 | ||||
| chr6:144285223-144285372 | Common:2; Rare:39 | ||||
| chr6:144286083-144286366 | Common:3; Rare:55 | ||||
| chr6:145814709-145814895 | Common:1; Rare:90 | ||||
| chr6:145964295-145964553 | Common:1; Rare:88 | ||||
| chr6:149546006-149546191 | Common:1; Rare:80 | ||||
| chr6:149648584-149648814 | Common:1; Rare:72 | ||||
| chr6:149718055-149718191 | Common:3; Rare:48 | ||||
| chr6:149749545-149749796 | Rare:115 | ||||
| chr6:149963824-149964007 | Common:1; Rare:53 | ||||
| chr6:150866346-150866521 | Rare:68 | ||||
| chr6:151325475-151325686 | Common:2; Rare:52 | ||||
| chr6:151391516-151391809 | Common:3; Rare:75 | ||||
| chr6:151452019-151452538 | Common:5; Rare:183; Clinvar (benign):3 |