| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:144078492-144078722 | Common:1; Rare:74 | ||||
| chr8:144082490-144082671 | Common:2; Rare:59 | ||||
| chr8:144096152-144096388 | Common:1; Rare:90; Clinvar (benign):3 | ||||
| chr8:144103713-144103896 | Rare:60 | ||||
| chr8:144104196-144104496 | Common:2; Rare:90 | ||||
| chr8:144292564-144292723 | Rare:37 | ||||
| chr8:144373788-144374066 | Common:3; Rare:92 | ||||
| chr8:144413516-144413673 | Rare:58; Clinvar:1 | ||||
| chr8:144528560-144528759 | Common:7; Rare:47 | ||||
| chr8:144755461-144755709 | Common:1; Rare:84 | ||||
| chr8:144787311-144787386 | Rare:23 | ||||
| chr8:144792335-144792623 | Common:3; Rare:113 | ||||
| chr9:2844051-2844339 | Common:5; Rare:106 | ||||
| chr9:3526425-3526511 | Common:1; Rare:45 | ||||
| chr9:4679437-4679669 | Rare:108 |