Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:22814772-22814850 | Rare:33 | ||||
chr16:23453097-23453227 | Rare:39 | ||||
chr16:23557299-23557745 | Common:3; Rare:163; Clinvar:1; Clinvar (benign):2 | ||||
chr16:23641223-23641567 | Common:2; Rare:98; Clinvar:1; Clinvar (benign):3 | ||||
chr16:23678665-23678962 | Common:5; Rare:91 | ||||
chr16:23694852-23695189 | Rare:140 | ||||
chr16:23713196-23713314 | Rare:40 | ||||
chr16:23835817-23836001 | Common:1; Rare:68 | ||||
chr16:24729332-24729859 | Common:8; Rare:171 | ||||
chr16:25015254-25015458 | Common:2; Rare:69 | ||||
chr16:25111478-25111855 | Common:2; Rare:111 | ||||
chr16:25257474-25257577 | Rare:32 | ||||
chr16:25257817-25258008 | Common:3; Rare:85 | ||||
chr16:25691900-25692005 | Rare:34 | ||||
chr16:27203409-27203578 | Rare:59 |