| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:6632996-6633318 | Common:6; Rare:102; Clinvar:7; Clinvar (benign):3 | ||||
| chr5:7869000-7869209 | Common:2; Rare:106; Clinvar (benign):1 | ||||
| chr5:9546033-9546372 | Common:8; Rare:79 | ||||
| chr5:10249866-10250179 | Common:16; Rare:146 | ||||
| chr5:10250187-10250427 | Common:3; Rare:115; Clinvar:5; Clinvar (benign):2 | ||||
| chr5:10353590-10353955 | Common:3; Rare:137 | ||||
| chr5:16465706-16465951 | Common:1; Rare:56 | ||||
| chr5:16936196-16936492 | Common:3; Rare:96 | ||||
| chr5:31532032-31532381 | Common:3; Rare:100 | ||||
| chr5:32174277-32174437 | Common:2; Rare:58 | ||||
| chr5:32444662-32444949 | Common:1; Rare:110 | ||||
| chr5:33440606-33441117 | Common:7; Rare:143 | ||||
| chr5:33891917-33892289 | Rare:84 | ||||
| chr5:34656087-34656473 | Common:4; Rare:107 | ||||
| chr5:34915218-34915355 | Rare:38 |