| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:4775522-4775691 | Common:4; Rare:81; Clinvar:1 | ||||
| chr7:4882214-4882449 | Rare:47 | ||||
| chr7:5190023-5190247 | Common:1; Rare:93 | ||||
| chr7:5513746-5513886 | Common:1; Rare:61 | ||||
| chr7:5593353-5593448 | Rare:26 | ||||
| chr7:6009018-6009496 | Common:4; Rare:228; Clinvar:11; Clinvar (benign):15; Clinvar (pathogenic):1 | ||||
| chr7:6104627-6104966 | Common:5; Rare:125 | ||||
| chr7:6400027-6400186 | Rare:36 | ||||
| chr7:6447885-6448087 | Common:2; Rare:80 | ||||
| chr7:6484038-6484289 | Common:2; Rare:122 | ||||
| chr7:6577382-6577523 | Rare:49 | ||||
| chr7:7183011-7183321 | Common:1; Rare:97 | ||||
| chr7:7566753-7567073 | Common:5; Rare:127 | ||||
| chr7:8262130-8262367 | Rare:96 | ||||
| chr7:10973744-10973928 | Rare:79 |