| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:34426010-34426205 | Common:5; Rare:83; Clinvar:1; Clinvar (benign):8 | ||||
| chr6:34696714-34696995 | Common:1; Rare:66 | ||||
| chr6:34757315-34757550 | Common:1; Rare:68 | ||||
| chr6:34887908-34888111 | Common:1; Rare:58 | ||||
| chr6:35259382-35259778 | Common:3; Rare:127 | ||||
| chr6:35468284-35468462 | Common:3; Rare:72 | ||||
| chr6:35921052-35921274 | Common:1; Rare:90 | ||||
| chr6:36442915-36443100 | Common:2; Rare:70 | ||||
| chr6:36547242-36547548 | Common:2; Rare:113 | ||||
| chr6:36839438-36839573 | Common:1; Rare:17 | ||||
| chr6:36874769-36874902 | Rare:48 | ||||
| chr6:36874977-36875168 | Common:1; Rare:30 | ||||
| chr6:37257583-37257827 | Rare:63 | ||||
| chr6:37433085-37433294 | Common:3; Rare:62 | ||||
| chr6:37818985-37819137 | Common:1; Rare:51 |