| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:78867470-78867605 | Rare:62 | ||||
| chr6:79537340-79537676 | Common:2; Rare:107; Clinvar:4 | ||||
| chr6:79631156-79631358 | Common:2; Rare:51 | ||||
| chr6:83193194-83193395 | Common:3; Rare:67 | ||||
| chr6:85449974-85450083 | Common:1; Rare:28 | ||||
| chr6:85593812-85594064 | Common:1; Rare:78 | ||||
| chr6:85643817-85643918 | Common:2; Rare:33 | ||||
| chr6:87155240-87155591 | Rare:93 | ||||
| chr6:87472847-87472999 | Common:1; Rare:54; Clinvar (benign):4 | ||||
| chr6:87589946-87590165 | Common:2; Rare:100; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr6:88963545-88963830 | Common:2; Rare:95 | ||||
| chr6:89081022-89081365 | Common:2; Rare:136 | ||||
| chr6:89352609-89352999 | Common:3; Rare:92 | ||||
| chr6:89638419-89638530 | Common:1; Rare:21 | ||||
| chr6:89638721-89638829 | Common:3; Rare:38 |