| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:159000130-159000305 | Common:1; Rare:45 | ||||
| chr6:159693144-159693609 | Common:6; Rare:143 | ||||
| chr6:159726911-159727175 | Common:1; Rare:103 | ||||
| chr6:159727325-159727633 | Common:5; Rare:132 | ||||
| chr6:159762310-159762530 | Common:2; Rare:61 | ||||
| chr6:159789534-159789975 | Common:4; Rare:146 | ||||
| chr6:159790244-159790515 | Common:7; Rare:87 | ||||
| chr6:162727766-162728054 | Common:3; Rare:77; Clinvar:1 | ||||
| chr6:166342505-166342659 | Common:3; Rare:61 | ||||
| chr6:166999061-166999415 | Common:1; Rare:120 | ||||
| chr6:167826823-167827123 | Common:2; Rare:164 | ||||
| chr6:169701984-169702149 | Common:1; Rare:73 | ||||
| chr6:169751521-169751645 | Rare:45; Clinvar (benign):1 | ||||
| chr6:170554162-170554445 | Common:2; Rare:86 | ||||
| chr7:519148-519294 | Rare:40 |