| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:85643752-85643983 | Common:3; Rare:72 | ||||
| chr6:87155277-87155631 | Rare:105 | ||||
| chr6:87156071-87156272 | Rare:67 | ||||
| chr6:87472897-87473010 | Common:1; Rare:44; Clinvar (benign):4 | ||||
| chr6:87518607-87518859 | Common:1; Rare:81; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):5 | ||||
| chr6:87589744-87590180 | Common:3; Rare:191; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr6:87700932-87701027 | Common:1; Rare:18 | ||||
| chr6:87701450-87701723 | Common:1; Rare:92 | ||||
| chr6:87701874-87702013 | Rare:46 | ||||
| chr6:88963549-88963826 | Common:2; Rare:93 | ||||
| chr6:89081008-89081411 | Common:2; Rare:156 | ||||
| chr6:89352611-89353008 | Common:2; Rare:93 | ||||
| chr6:89638410-89638549 | Common:1; Rare:32 | ||||
| chr6:89638685-89638772 | Common:3; Rare:38 | ||||
| chr6:89819720-89819896 | Rare:61 |