| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:37808284-37808636 | Common:1; Rare:82 | ||||
| chr1:37859575-37859836 | Common:4; Rare:94 | ||||
| chr1:37989954-37990129 | Rare:70 | ||||
| chr1:38012461-38012819 | Common:1; Rare:110 | ||||
| chr1:38873282-38873563 | Common:3; Rare:95 | ||||
| chr1:39026240-39026397 | Common:1; Rare:41 | ||||
| chr1:39738701-39738907 | Common:2; Rare:44 | ||||
| chr1:39883447-39883570 | Common:1; Rare:51; Clinvar (pathogenic):1 | ||||
| chr1:39954983-39955170 | Common:1; Rare:50 | ||||
| chr1:40040444-40040851 | Common:3; Rare:125 | ||||
| chr1:40097163-40097316 | Rare:69; Clinvar:6; Clinvar (benign):3; Clinvar (pathogenic):5 | ||||
| chr1:40161272-40161405 | Rare:34 | ||||
| chr1:40257877-40258332 | Common:4; Rare:132; Clinvar:8; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr1:40373536-40373774 | Common:1; Rare:61 | ||||
| chr1:40449983-40450190 | Common:3; Rare:79 |