| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:143450654-143450944 | Common:1; Rare:107; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:143511651-143511755 | Common:3; Rare:27 | ||||
| chr6:143773801-143774103 | Common:1; Rare:73 | ||||
| chr6:143843168-143843398 | Common:2; Rare:74 | ||||
| chr6:144150316-144150523 | Common:5; Rare:60 | ||||
| chr6:144285242-144285510 | Common:2; Rare:60 | ||||
| chr6:144286142-144286434 | Common:4; Rare:53 | ||||
| chr6:145814663-145814922 | Common:1; Rare:115 | ||||
| chr6:147204364-147204482 | Rare:32 | ||||
| chr6:147204542-147204630 | Rare:28 | ||||
| chr6:148342913-148343178 | Common:1; Rare:96 | ||||
| chr6:149484853-149485189 | Common:4; Rare:63 | ||||
| chr6:149546010-149546149 | Rare:59 | ||||
| chr6:149717650-149717702 | Rare:16 | ||||
| chr6:149717711-149717770 | Rare:18 |