| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:7068030-7068394 | Common:7; Rare:124 | ||||
| chr4:15655295-15655473 | Common:1; Rare:81 | ||||
| chr4:15681445-15681875 | Common:4; Rare:148 | ||||
| chr4:17614548-17614651 | Common:2; Rare:44 | ||||
| chr4:17810701-17811039 | Common:3; Rare:105 | ||||
| chr4:24584472-24584730 | Common:1; Rare:80 | ||||
| chr4:25160385-25160725 | Common:3; Rare:96; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25914029-25914283 | Common:2; Rare:111 | ||||
| chr4:26583984-26584120 | Rare:26 | ||||
| chr4:37826466-37826728 | Common:7; Rare:86 | ||||
| chr4:39458849-39459112 | Common:3; Rare:149; Clinvar (benign):5 | ||||
| chr4:39527410-39527754 | Common:2; Rare:85 | ||||
| chr4:39638847-39639140 | Common:1; Rare:109 | ||||
| chr4:39697970-39698174 | Common:1; Rare:82 | ||||
| chr4:41990402-41990572 | Common:1; Rare:62 |