| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:7389753-7389976 | Common:1; Rare:54 | ||||
| chr6:7541390-7541902 | Common:1; Rare:150; Clinvar:3; Clinvar (benign):2 | ||||
| chr6:7910622-7910923 | Common:4; Rare:121 | ||||
| chr6:8064309-8064593 | Common:4; Rare:94 | ||||
| chr6:8102505-8102712 | Common:1; Rare:71 | ||||
| chr6:8435440-8435678 | Common:5; Rare:89 | ||||
| chr6:10694599-10694988 | Common:4; Rare:103 | ||||
| chr6:10722927-10723241 | Common:5; Rare:119 | ||||
| chr6:10747582-10747881 | Common:3; Rare:111 | ||||
| chr6:11044238-11044629 | Common:3; Rare:127 | ||||
| chr6:11093644-11093834 | Rare:62 | ||||
| chr6:11232612-11232825 | Rare:45 | ||||
| chr6:13328515-13328621 | Common:2; Rare:36 | ||||
| chr6:13615170-13615624 | Common:2; Rare:180 | ||||
| chr6:13814015-13814183 | Common:2; Rare:34 |