| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:45500107-45500359 | Rare:59; Clinvar:4; Clinvar (pathogenic):3 | ||||
| chr1:45521827-45522040 | Common:1; Rare:87 | ||||
| chr1:45550721-45550879 | Common:1; Rare:46 | ||||
| chr1:45583809-45584070 | Common:1; Rare:86 | ||||
| chr1:45687059-45687317 | Common:1; Rare:70 | ||||
| chr1:45688059-45688258 | Common:1; Rare:57 | ||||
| chr1:45750615-45750728 | Rare:38 | ||||
| chr1:46132853-46133264 | Common:3; Rare:114 | ||||
| chr1:46198347-46198522 | Common:1; Rare:73; Clinvar:1; Clinvar (benign):1 | ||||
| chr1:46203249-46203374 | Rare:29 | ||||
| chr1:46303243-46303784 | Common:2; Rare:170 | ||||
| chr1:46340672-46340821 | Common:3; Rare:41 | ||||
| chr1:47023494-47023830 | Common:2; Rare:81 | ||||
| chr1:47314093-47314406 | Common:3; Rare:65; Clinvar:1 | ||||
| chr1:47333767-47333979 | Common:2; Rare:74 |