Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:173356236-173356400 | Common:3; Rare:25 | ||||
chr2:176637607-176637762 | Common:3; Rare:60 | ||||
chr2:177214859-177215141 | Rare:79 | ||||
chr2:177215326-177215945 | Common:4; Rare:153 | ||||
chr2:177234158-177234363 | Rare:54; Clinvar:2 | ||||
chr2:178304400-178304627 | Common:1; Rare:40 | ||||
chr2:181773654-181773836 | Rare:38 | ||||
chr2:186174061-186174154 | Common:1; Rare:9 | ||||
chr2:190491360-190491482 | Rare:17 | ||||
chr2:190503176-190503511 | Common:1; Rare:57 | ||||
chr2:190649826-190650181 | Rare:72 | ||||
chr2:190942330-190942356 | Rare:4 | ||||
chr2:197489182-197489489 | Common:1; Rare:71; Clinvar (benign):1 | ||||
chr2:197693533-197693576 | Common:1; Rare:12 | ||||
chr2:202376111-202376292 | Rare:94 |