| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:106316183-106316601 | Common:5; Rare:135 | ||||
| chr4:107720181-107720518 | Common:7; Rare:136 | ||||
| chr4:107989690-107989942 | Common:5; Rare:112; Clinvar:4; Clinvar (benign):5 | ||||
| chr4:108620388-108620718 | Common:6; Rare:148 | ||||
| chr4:109433535-109433631 | Rare:24 | ||||
| chr4:109433757-109433920 | Common:1; Rare:57 | ||||
| chr4:109730062-109730237 | Common:2; Rare:42 | ||||
| chr4:109815380-109815553 | Common:1; Rare:46 | ||||
| chr4:109815749-109815798 | Rare:12 | ||||
| chr4:110198521-110198709 | Rare:54 | ||||
| chr4:112636880-112637182 | Common:1; Rare:82 | ||||
| chr4:112637394-112637581 | Common:3; Rare:49 | ||||
| chr4:113761129-113761272 | Common:1; Rare:34 | ||||
| chr4:113978965-113979181 | Common:3; Rare:33 | ||||
| chr4:113979569-113979817 | Common:6; Rare:60 |