| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:9877891-9878084 | Common:1; Rare:29 | ||||
| chr1:9893259-9893615 | Rare:62 | ||||
| chr1:9942783-9942921 | Common:1; Rare:23 | ||||
| chr1:9943012-9943125 | Common:1; Rare:28 | ||||
| chr1:9943247-9943492 | Common:3; Rare:63 | ||||
| chr1:10032763-10032996 | Rare:63 | ||||
| chr1:10398857-10399132 | Common:2; Rare:106 | ||||
| chr1:10399316-10399557 | Common:3; Rare:50 | ||||
| chr1:10399856-10400187 | Common:3; Rare:61 | ||||
| chr1:11099772-11100026 | Common:2; Rare:101 | ||||
| chr1:11262490-11262828 | Common:2; Rare:104 | ||||
| chr1:11273249-11273552 | Common:2; Rare:85; Clinvar:2; Clinvar (benign):2 | ||||
| chr1:11654396-11654541 | Rare:36 | ||||
| chr1:11654826-11654925 | Common:1; Rare:24 | ||||
| chr1:11805900-11806278 | Common:2; Rare:102; Clinvar:1 |