Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr21:46659513-46659733 | Common:2; Rare:47 | ||||
chr21:46659910-46660025 | Rare:24 | ||||
chr22:17097046-17097079 | Rare:8; Clinvar (benign):1 | ||||
chr22:17639567-17639814 | Common:3; Rare:62 | ||||
chr22:17969837-17970065 | Common:1; Rare:52 | ||||
chr22:17972743-17972875 | Common:1; Rare:25 | ||||
chr22:19176690-19176874 | Common:1; Rare:71; Clinvar:1; Clinvar (benign):1 | ||||
chr22:19197964-19198038 | Common:1; Rare:11 | ||||
chr22:19331906-19331929 | Rare:5 | ||||
chr22:19943530-19943574 | Common:1; Rare:7 | ||||
chr22:19953331-19953577 | Common:2; Rare:56 | ||||
chr22:20058721-20058789 | Rare:8 | ||||
chr22:20206301-20206402 | Common:1; Rare:24 | ||||
chr22:20315428-20315606 | Rare:55 | ||||
chr22:20428205-20428494 | Common:7; Rare:61 |