| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:915735-915822 | Rare:25 | ||||
| chr4:932099-932492 | Common:2; Rare:148 | ||||
| chr4:986930-987197 | Common:3; Rare:88; Clinvar:3; Clinvar (benign):3 | ||||
| chr4:1289644-1289916 | Common:1; Rare:92 | ||||
| chr4:1720550-1720634 | Rare:26 | ||||
| chr4:1721325-1721529 | Common:2; Rare:58 | ||||
| chr4:2008964-2009027 | Rare:33 | ||||
| chr4:2041885-2042022 | Common:1; Rare:52 | ||||
| chr4:2468869-2469183 | Common:4; Rare:119 | ||||
| chr4:2812182-2812319 | Rare:23 | ||||
| chr4:2843678-2844000 | Common:3; Rare:120 | ||||
| chr4:2875665-2876026 | Common:1; Rare:89 | ||||
| chr4:2934777-2934928 | Common:4; Rare:71 | ||||
| chr4:2963322-2963596 | Common:2; Rare:101 | ||||
| chr4:3532264-3532326 | Rare:20 |