Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:46916025-46916197 | Common:2; Rare:52 | ||||
chr2:47176178-47176319 | Common:2; Rare:52 | ||||
chr2:47176335-47176941 | Common:7; Rare:282; Clinvar (benign):5 | ||||
chr2:47344956-47345210 | Common:1; Rare:70 | ||||
chr2:47369474-47369559 | Common:2; Rare:47; Clinvar:5; Clinvar (benign):4 | ||||
chr2:47402903-47403209 | Common:1; Rare:142; Clinvar:47; Clinvar (benign):32; Clinvar (pathogenic):1 | ||||
chr2:47570011-47570135 | Rare:27 | ||||
chr2:47570945-47571013 | Rare:19 | ||||
chr2:47782950-47783214 | Common:2; Rare:119; Clinvar:6; Clinvar (benign):10 | ||||
chr2:47783759-47783952 | Common:5; Rare:39; Clinvar (benign):1 | ||||
chr2:47905491-47905848 | Common:3; Rare:176 | ||||
chr2:47906054-47906197 | Common:1; Rare:43 | ||||
chr2:48314364-48314814 | Rare:161 | ||||
chr2:48440609-48440925 | Common:8; Rare:137 | ||||
chr2:49973990-49974315 | Common:2; Rare:107 |