| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:25914051-25914301 | Common:2; Rare:106 | ||||
| chr4:26319364-26319688 | Rare:88 | ||||
| chr4:26320590-26320826 | Common:1; Rare:86 | ||||
| chr4:26320946-26321041 | Rare:39 | ||||
| chr4:26583981-26584120 | Rare:28 | ||||
| chr4:26857443-26857776 | Common:4; Rare:92 | ||||
| chr4:26860444-26860665 | Common:2; Rare:71 | ||||
| chr4:37826571-37826729 | Common:1; Rare:57 | ||||
| chr4:37977142-37977470 | Rare:85 | ||||
| chr4:38782921-38783008 | Common:1; Rare:20 | ||||
| chr4:39458856-39459133 | Common:3; Rare:158; Clinvar:1; Clinvar (benign):5 | ||||
| chr4:39527537-39527761 | Common:1; Rare:58 | ||||
| chr4:39697936-39698192 | Common:2; Rare:109 | ||||
| chr4:40056662-40056976 | Common:4; Rare:99 | ||||
| chr4:40192847-40192960 | Common:1; Rare:17 |