| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:88823134-88823341 | Common:3; Rare:33 | ||||
| chr4:89111360-89111641 | Common:4; Rare:100 | ||||
| chr4:94757739-94758053 | Common:4; Rare:85 | ||||
| chr4:95548992-95549168 | Common:1; Rare:41 | ||||
| chr4:98143468-98143638 | Common:1; Rare:41 | ||||
| chr4:98261194-98261499 | Common:1; Rare:95 | ||||
| chr4:98929101-98929242 | Common:3; Rare:43 | ||||
| chr4:98995356-98995837 | Common:6; Rare:160 | ||||
| chr4:99088689-99088917 | Common:7; Rare:111 | ||||
| chr4:99563601-99563805 | Common:2; Rare:62 | ||||
| chr4:99563911-99564165 | Common:2; Rare:83; Clinvar:2; Clinvar (benign):2 | ||||
| chr4:99894357-99894600 | Common:2; Rare:88 | ||||
| chr4:99946529-99946846 | Rare:113 | ||||
| chr4:99950188-99950482 | Common:1; Rare:77 | ||||
| chr4:101346920-101347075 | Common:1; Rare:36 |