| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:32661070-32661398 | Common:58; Rare:27 | ||||
| chr6:32690291-32690473 | Common:4; Rare:20 | ||||
| chr6:32812570-32812950 | Common:3; Rare:56 | ||||
| chr6:32833900-32834065 | Common:1; Rare:20 | ||||
| chr6:32853192-32853238 | Common:1; Rare:17; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:32853281-32853298 | Rare:4 | ||||
| chr6:32894581-32894827 | Common:7; Rare:70 | ||||
| chr6:32930986-32931118 | Rare:16 | ||||
| chr6:32974355-32974583 | Common:5; Rare:73; Clinvar:1 | ||||
| chr6:33018816-33019220 | Common:9; Rare:63 | ||||
| chr6:33029473-33029758 | Common:3; Rare:39 | ||||
| chr6:33072697-33072979 | Common:13; Rare:39 | ||||
| chr6:33077763-33077854 | Common:1; Rare:16 | ||||
| chr6:33112140-33112486 | Common:7; Rare:60 | ||||
| chr6:33249235-33249624 | Rare:119 |