| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:35557622-35557845 | Common:2; Rare:85 | ||||
| chr1:36155976-36156210 | Rare:98 | ||||
| chr1:37808180-37808540 | Common:1; Rare:84 | ||||
| chr1:38012523-38012799 | Rare:83 | ||||
| chr1:38859701-38860033 | Rare:125 | ||||
| chr1:38873306-38873563 | Common:3; Rare:91 | ||||
| chr1:40040444-40040794 | Common:3; Rare:104 | ||||
| chr1:40257909-40258276 | Common:4; Rare:99; Clinvar:7 | ||||
| chr1:40508666-40508794 | Common:3; Rare:36 | ||||
| chr1:40691493-40691630 | Common:2; Rare:66 | ||||
| chr1:42456216-42456571 | Common:1; Rare:104 | ||||
| chr1:42767013-42767301 | Common:4; Rare:89; Clinvar (benign):1 | ||||
| chr1:42816961-42817141 | Common:1; Rare:52 | ||||
| chr1:42846401-42846652 | Common:1; Rare:70 | ||||
| chr1:42958821-42959030 | Common:2; Rare:50; Clinvar:3; Clinvar (benign):3 |