| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:33441090-33441550 | Common:4; Rare:281 | ||||
| chr5:33441815-33442215 | Common:4; Rare:68 | ||||
| chr5:33984535-33984935 | Common:3; Rare:204 | ||||
| chr5:34007584-34008380 | Common:21; Rare:1001; Clinvar:30; Clinvar (benign):20; Clinvar (pathogenic):4 | ||||
| chr5:34655410-34655860 | Common:1; Rare:127 | ||||
| chr5:34656091-34656749 | Common:21; Rare:554 | ||||
| chr5:34656836-34657236 | Common:3; Rare:95 | ||||
| chr5:34686770-34687220 | Common:2; Rare:173 | ||||
| chr5:34687310-34687630 | Common:4; Rare:46 | ||||
| chr5:34838927-34839601 | Common:29; Rare:820 | ||||
| chr5:34914650-34914922 | Rare:162 | ||||
| chr5:34915130-34915390 | Rare:247 | ||||
| chr5:34915413-34915869 | Common:8; Rare:595 | ||||
| chr5:34915771-34916171 | Common:7; Rare:125 | ||||
| chr5:34916556-34916956 | Common:1; Rare:103 |