Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:12617441-12617583 | Rare:22 | ||||
chr1:12617588-12618464 | Common:9; Rare:155 | ||||
chr1:13583707-13584278 | Common:4; Rare:248 | ||||
chr1:13749150-13749455 | Common:2; Rare:109 | ||||
chr1:15409734-15409902 | Common:1; Rare:51 | ||||
chr1:15410186-15410279 | Rare:26 | ||||
chr1:15456684-15456734 | Common:1; Rare:12 | ||||
chr1:15526550-15526913 | Common:2; Rare:117 | ||||
chr1:16017763-16018144 | Common:5; Rare:139 | ||||
chr1:16352410-16352575 | Common:2; Rare:91 | ||||
chr1:16613468-16613836 | Common:6; Rare:1 | ||||
chr1:17053960-17054368 | Common:3; Rare:126; Clinvar:16; Clinvar (benign):10 | ||||
chr1:17119444-17119569 | Rare:32 | ||||
chr1:17618209-17618424 | Common:2; Rare:50 | ||||
chr1:18902759-18902992 | Common:3; Rare:51 |