Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:2777235-2777380 | Common:1; Rare:58 | ||||
chr16:3112584-3112603 | Rare:6 | ||||
chr16:3134861-3135126 | Common:2; Rare:67 | ||||
chr16:3305391-3305494 | Common:1; Rare:38 | ||||
chr16:3400975-3401215 | Common:5; Rare:88 | ||||
chr16:3443505-3443725 | Common:2; Rare:70 | ||||
chr16:4371688-4371860 | Rare:63 | ||||
chr16:4425767-4425879 | Common:1; Rare:52 | ||||
chr16:4538427-4538562 | Common:1; Rare:42 | ||||
chr16:8797631-8797866 | Rare:88; Clinvar:2; Clinvar (benign):1 | ||||
chr16:8868986-8869247 | Common:4; Rare:118 | ||||
chr16:10944326-10944630 | Common:1; Rare:93 | ||||
chr16:11586903-11587030 | Common:1; Rare:41 | ||||
chr16:11851517-11851614 | Rare:49 | ||||
chr16:11976648-11976769 | Rare:45 |