| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:185143136-185143310 | Common:2; Rare:58; Clinvar (benign):3 | ||||
| chr4:185203906-185204098 | Common:1; Rare:64 | ||||
| chr4:185210648-185210831 | Common:2; Rare:27 | ||||
| chr4:185395901-185396039 | Rare:44 | ||||
| chr4:185396561-185396843 | Rare:91 | ||||
| chr4:185425866-185426268 | Common:4; Rare:124 | ||||
| chr4:185535421-185535632 | Common:1; Rare:73; Clinvar:1; Clinvar (benign):4 | ||||
| chr4:185811701-185811856 | Common:1; Rare:33 | ||||
| chr4:185812150-185812518 | Common:1; Rare:72 | ||||
| chr4:185933063-185933501 | Common:1; Rare:75 | ||||
| chr4:186068891-186069202 | Common:4; Rare:60 | ||||
| chr4:186191442-186191841 | Common:6; Rare:128; Clinvar:2; Clinvar (benign):5 | ||||
| chr4:186723759-186723952 | Common:5; Rare:78 | ||||
| chr4:186726616-186726925 | Common:4; Rare:101 | ||||
| chr4:188109327-188109448 | Rare:33 |