Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:68182048-68182106 | Common:9; Rare:18 | ||||
chr2:69014882-69015090 | Common:1; Rare:32 | ||||
chr2:69044649-69044812 | Rare:38; Clinvar (pathogenic):1 | ||||
chr2:69063355-69063469 | Rare:18 | ||||
chr2:69445531-69445829 | Common:1; Rare:33 | ||||
chr2:69498010-69498315 | Common:1; Rare:52 | ||||
chr2:69526095-69526358 | Common:2; Rare:42 | ||||
chr2:69642672-69642764 | Common:1; Rare:18 | ||||
chr2:69804244-69804625 | Rare:87 | ||||
chr2:70086265-70086378 | Common:2; Rare:49 | ||||
chr2:70088436-70088860 | Common:1; Rare:97 | ||||
chr2:70088901-70089072 | Rare:52 | ||||
chr2:70124309-70124371 | Rare:13 | ||||
chr2:70275322-70275551 | Rare:54 | ||||
chr2:70281101-70281436 | Common:1; Rare:81 |