| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:122471768-122471925 | Common:2; Rare:45 | ||||
| chr6:127266811-127266971 | Common:1; Rare:64 | ||||
| chr6:127343334-127343429 | Rare:19 | ||||
| chr6:143060738-143060895 | Common:7; Rare:50 | ||||
| chr6:143450648-143450882 | Common:1; Rare:96; Clinvar:3; Clinvar (benign):1 | ||||
| chr6:144095075-144095233 | Common:1; Rare:40 | ||||
| chr6:144150302-144150564 | Common:5; Rare:71 | ||||
| chr6:144285130-144285335 | Common:2; Rare:67 | ||||
| chr6:149941808-149942041 | Common:6; Rare:45 | ||||
| chr6:153002664-153002841 | Common:3; Rare:60 | ||||
| chr6:158168244-158168393 | Common:2; Rare:54 | ||||
| chr6:159726929-159727167 | Common:1; Rare:90 | ||||
| chr6:159727330-159727575 | Common:5; Rare:108 | ||||
| chr6:159789425-159789471 | Rare:20 | ||||
| chr6:159789599-159789947 | Common:2; Rare:118 |