| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:42217848-42217967 | Common:2; Rare:30 | ||||
| chr6:42452010-42452323 | Common:3; Rare:53 | ||||
| chr6:42746074-42746335 | Rare:71 | ||||
| chr6:42879831-42879940 | Rare:46 | ||||
| chr6:42890802-42891051 | Rare:83 | ||||
| chr6:42929197-42929562 | Common:4; Rare:104 | ||||
| chr6:42984284-42984609 | Rare:80 | ||||
| chr6:43013822-43014329 | Common:2; Rare:126 | ||||
| chr6:43182160-43182216 | Rare:14 | ||||
| chr6:43308796-43309011 | Common:1; Rare:62 | ||||
| chr6:43427603-43427893 | Rare:62 | ||||
| chr6:43477327-43477589 | Common:2; Rare:50 | ||||
| chr6:43516877-43517112 | Common:4; Rare:90; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:43575962-43576185 | Rare:87; Clinvar:4 | ||||
| chr6:43687768-43687865 | Common:1; Rare:41 |