| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:97764444-97764802 | Common:1; Rare:83; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:97821915-97822092 | Rare:62 | ||||
| chr3:97972361-97972484 | Common:3; Rare:47 | ||||
| chr3:98522598-98522755 | Rare:36 | ||||
| chr3:98522847-98523130 | Common:1; Rare:85 | ||||
| chr3:98901647-98901979 | Common:1; Rare:122 | ||||
| chr3:99638357-99638527 | Common:1; Rare:39 | ||||
| chr3:99638529-99638669 | Rare:31 | ||||
| chr3:99638714-99639000 | Common:1; Rare:52 | ||||
| chr3:99817548-99818040 | Rare:151 | ||||
| chr3:100260704-100261042 | Rare:96 | ||||
| chr3:100334666-100334786 | Common:1; Rare:56 | ||||
| chr3:100401348-100401616 | Common:1; Rare:61 | ||||
| chr3:100492422-100492658 | Common:2; Rare:78 | ||||
| chr3:100709171-100709721 | Common:9; Rare:164; Clinvar (benign):1 |