| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:159693148-159693614 | Common:6; Rare:143 | ||||
| chr6:159726911-159727162 | Common:1; Rare:97 | ||||
| chr6:159727322-159727640 | Common:5; Rare:135 | ||||
| chr6:159789553-159789947 | Common:3; Rare:134 | ||||
| chr6:159790272-159790550 | Common:8; Rare:98 | ||||
| chr6:162727736-162727974 | Rare:67; Clinvar:1 | ||||
| chr6:166342508-166342665 | Common:3; Rare:61 | ||||
| chr6:166956539-166956728 | Common:4; Rare:71; Clinvar:3 | ||||
| chr6:166999037-166999405 | Common:1; Rare:128 | ||||
| chr6:168441041-168441399 | Common:4; Rare:101 | ||||
| chr6:169253722-169254139 | Common:1; Rare:71 | ||||
| chr6:169702013-169702138 | Common:1; Rare:50 | ||||
| chr6:169751525-169751643 | Rare:41; Clinvar (benign):1 | ||||
| chr6:170553207-170553351 | Common:2; Rare:68 | ||||
| chr6:170554211-170554428 | Common:1; Rare:68 |