| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:2468853-2469154 | Common:3; Rare:104 | ||||
| chr4:2843721-2843970 | Common:3; Rare:82 | ||||
| chr4:2934783-2935024 | Common:5; Rare:103 | ||||
| chr4:4248214-4248305 | Common:2; Rare:35 | ||||
| chr4:4290161-4290247 | Common:1; Rare:24 | ||||
| chr4:4541989-4542158 | Common:1; Rare:70 | ||||
| chr4:6987024-6987292 | Common:1; Rare:84 | ||||
| chr4:15681463-15681869 | Common:3; Rare:140 | ||||
| chr4:17810701-17811065 | Common:4; Rare:114 | ||||
| chr4:25160388-25160704 | Common:3; Rare:91; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:26320874-26321038 | Rare:54; Clinvar (benign):1 | ||||
| chr4:38867565-38867816 | Common:2; Rare:84 | ||||
| chr4:39458876-39459112 | Common:2; Rare:132; Clinvar (benign):5 | ||||
| chr4:39527531-39527754 | Common:1; Rare:56 | ||||
| chr4:39638847-39639140 | Common:1; Rare:109 |