| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:25377001-25377349 | Common:3; Rare:106 | ||||
| chr4:25913932-25914327 | Common:3; Rare:169 | ||||
| chr4:26320438-26320863 | Common:1; Rare:143 | ||||
| chr4:26320900-26321057 | Rare:57; Clinvar (benign):1 | ||||
| chr4:37826538-37826744 | Common:6; Rare:75 | ||||
| chr4:39458834-39459142 | Common:3; Rare:170; Clinvar:1; Clinvar (benign):5 | ||||
| chr4:39527383-39527755 | Common:2; Rare:91 | ||||
| chr4:39638847-39639140 | Common:1; Rare:109 | ||||
| chr4:39697930-39698192 | Common:2; Rare:112 | ||||
| chr4:39977339-39977639 | Common:2; Rare:86 | ||||
| chr4:40056673-40056998 | Common:4; Rare:103 | ||||
| chr4:40629457-40629614 | Common:1; Rare:25 | ||||
| chr4:40629811-40630036 | Common:1; Rare:53 | ||||
| chr4:40630582-40630861 | Common:2; Rare:62 | ||||
| chr4:40749795-40750242 | Common:3; Rare:123 |