| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:52284635-52285019 | Common:4; Rare:263 | ||||
| chr6:52361993-52362291 | Common:8; Rare:159 | ||||
| chr6:52362477-52362877 | Rare:118 | ||||
| chr6:52420089-52420385 | Common:6; Rare:247; Clinvar:2; Clinvar (benign):4 | ||||
| chr6:52576930-52577466 | Common:15; Rare:320 | ||||
| chr6:52670992-52671219 | Rare:105 | ||||
| chr6:53061672-53061984 | Rare:136 | ||||
| chr6:53065297-53065534 | Common:2; Rare:138 | ||||
| chr6:53348856-53349260 | Common:4; Rare:287 | ||||
| chr6:53544551-53544751 | Rare:102 | ||||
| chr6:53544990-53545304 | Common:2; Rare:175; Clinvar (benign):2 | ||||
| chr6:53794140-53794540 | Common:8; Rare:117 | ||||
| chr6:53794536-53794740 | Common:2; Rare:60 | ||||
| chr6:56393983-56394257 | Common:3; Rare:96 | ||||
| chr6:56542688-56543061 | Common:3; Rare:110 |