Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:87765929-87766044 | Rare:43 | ||||
chr16:88570174-88570420 | Common:1; Rare:88 | ||||
chr16:88663068-88663346 | Common:6; Rare:106 | ||||
chr16:88856913-88857143 | Common:4; Rare:106; Clinvar:1; Clinvar (benign):2 | ||||
chr16:89508325-89508418 | Rare:50 | ||||
chr16:89686898-89686922 | Rare:8 | ||||
chr16:89972503-89972601 | Rare:29 | ||||
chr17:714825-714976 | Common:2; Rare:43 | ||||
chr17:752175-752360 | Common:2; Rare:71 | ||||
chr17:1516662-1516969 | Common:1; Rare:110 | ||||
chr17:1829823-1830008 | Common:3; Rare:78 | ||||
chr17:2303757-2303980 | Common:2; Rare:84 | ||||
chr17:2593863-2593957 | Common:1; Rare:31; Clinvar:1; Clinvar (benign):3 | ||||
chr17:3668552-3668815 | Common:2; Rare:103 | ||||
chr17:3723802-3724031 | Rare:128 |