| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:10747575-10747855 | Common:3; Rare:111 | ||||
| chr6:12008629-12008854 | Common:1; Rare:50 | ||||
| chr6:13328488-13328615 | Common:4; Rare:56 | ||||
| chr6:13574442-13574632 | Common:1; Rare:46 | ||||
| chr6:13615156-13615470 | Common:3; Rare:131 | ||||
| chr6:15245830-15245997 | Rare:44 | ||||
| chr6:16761404-16761726 | Common:2; Rare:96 | ||||
| chr6:17600765-17600965 | Common:14; Rare:77 | ||||
| chr6:17706377-17706450 | Rare:42 | ||||
| chr6:17706857-17707128 | Common:1; Rare:80 | ||||
| chr6:18122616-18122763 | Common:1; Rare:33; Clinvar (benign):2 | ||||
| chr6:20212343-20212592 | Common:2; Rare:65 | ||||
| chr6:20401541-20401916 | Common:3; Rare:94 | ||||
| chr6:20403368-20403811 | Common:1; Rare:107 | ||||
| chr6:20404031-20404295 | Common:2; Rare:50 |