Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:2047802-2048048 | Rare:118; Clinvar:2; Clinvar (benign):1 | ||||
chr16:2268069-2268165 | Rare:47 | ||||
chr16:2459954-2460145 | Common:1; Rare:53 | ||||
chr16:2537722-2538021 | Common:4; Rare:118 | ||||
chr16:2682350-2682666 | Rare:150 | ||||
chr16:2777117-2777392 | Common:2; Rare:113 | ||||
chr16:2980410-2980627 | Common:2; Rare:78 | ||||
chr16:3134861-3135125 | Common:2; Rare:67 | ||||
chr16:3305428-3305514 | Common:1; Rare:24 | ||||
chr16:3400965-3401251 | Common:6; Rare:104 | ||||
chr16:3443492-3443725 | Common:3; Rare:77 | ||||
chr16:3457946-3458076 | Common:2; Rare:62 | ||||
chr16:3577374-3577461 | Common:1; Rare:20 | ||||
chr16:3611572-3611804 | Rare:100 | ||||
chr16:4365014-4365340 | Common:1; Rare:88 |