| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:140107679-140107865 | Rare:64 | ||||
| chr5:140175011-140175285 | Common:2; Rare:66 | ||||
| chr5:140346362-140346721 | Common:2; Rare:83 | ||||
| chr5:140401393-140401935 | Common:3; Rare:124 | ||||
| chr5:140486771-140487034 | Rare:67 | ||||
| chr5:140564296-140564508 | Common:1; Rare:55 | ||||
| chr5:140564537-140564846 | Rare:81 | ||||
| chr5:140647551-140647924 | Common:5; Rare:156; Clinvar:4; Clinvar (benign):4 | ||||
| chr5:140675044-140675236 | Rare:51; Clinvar:1; Clinvar (benign):3 | ||||
| chr5:140691300-140691661 | Common:1; Rare:133; Clinvar:12; Clinvar (benign):2 | ||||
| chr5:141320742-141320910 | Common:1; Rare:56 | ||||
| chr5:141475924-141476028 | Rare:24 | ||||
| chr5:141476227-141476741 | Common:1; Rare:151 | ||||
| chr5:141625739-141625953 | Common:1; Rare:45 | ||||
| chr5:141636780-141637011 | Common:2; Rare:109 |