| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:3752157-3752255 | Common:1; Rare:32 | ||||
| chr6:3849163-3849448 | Common:3; Rare:78 | ||||
| chr6:4021216-4021432 | Rare:97 | ||||
| chr6:5003646-5003834 | Common:5; Rare:58 | ||||
| chr6:5004000-5004102 | Common:2; Rare:52 | ||||
| chr6:5132813-5132973 | Common:1; Rare:33 | ||||
| chr6:5260681-5261051 | Common:5; Rare:133; Clinvar (benign):4 | ||||
| chr6:5261263-5261553 | Common:9; Rare:72 | ||||
| chr6:6006835-6007102 | Common:3; Rare:60 | ||||
| chr6:7107601-7107995 | Common:1; Rare:130 | ||||
| chr6:7108553-7108674 | Common:1; Rare:40 | ||||
| chr6:7313100-7313391 | Common:5; Rare:107 | ||||
| chr6:7389390-7389510 | Rare:29 | ||||
| chr6:7389740-7390003 | Common:1; Rare:70 | ||||
| chr6:7541385-7541770 | Rare:118; Clinvar:2; Clinvar (benign):1 |