Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:86509604-86509617 | Rare:1 | ||||
chr16:87344601-87344775 | Common:1; Rare:43 | ||||
chr16:88759537-88759587 | Common:1; Rare:15 | ||||
chr17:7283046-7283192 | Rare:25 | ||||
chr17:7887472-7887796 | Rare:66 | ||||
chr17:8151483-8151491 | Rare:1 | ||||
chr17:8190060-8190372 | Common:1; Rare:103 | ||||
chr17:16061747-16062060 | Common:1; Rare:83 | ||||
chr17:16439528-16439692 | Rare:63 | ||||
chr17:17836209-17836418 | Common:3; Rare:58 | ||||
chr17:29677160-29677278 | Rare:8 | ||||
chr17:31008454-31008634 | Common:2; Rare:37 | ||||
chr17:38257267-38257438 | Common:1; Rare:64 | ||||
chr17:40120711-40120902 | Rare:39 | ||||
chr17:42422616-42422974 | Rare:143; Clinvar:4; Clinvar (pathogenic):2 |