| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:81752668-81752821 | Rare:77 | ||||
| chr6:82247704-82247964 | Common:1; Rare:86 | ||||
| chr6:83068028-83068154 | Common:1; Rare:31 | ||||
| chr6:83193194-83193433 | Common:3; Rare:79 | ||||
| chr6:83709074-83709353 | Common:4; Rare:82 | ||||
| chr6:85593693-85594007 | Common:1; Rare:104 | ||||
| chr6:85642799-85643112 | Common:4; Rare:103 | ||||
| chr6:85643817-85643946 | Common:2; Rare:40 | ||||
| chr6:87155234-87155649 | Rare:126 | ||||
| chr6:87472890-87473004 | Common:1; Rare:43; Clinvar (benign):4 | ||||
| chr6:87589920-87590186 | Common:3; Rare:138; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr6:87702193-87702528 | Common:2; Rare:108 | ||||
| chr6:88963513-88963830 | Common:2; Rare:98 | ||||
| chr6:89117926-89118122 | Common:3; Rare:84 | ||||
| chr6:89145963-89146090 | Rare:36 |