Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:1533487-1533815 | Common:1; Rare:70 | ||||
chr16:1706009-1706258 | Common:2; Rare:82 | ||||
chr16:1771499-1771864 | Common:3; Rare:143 | ||||
chr16:1773106-1773214 | Rare:34 | ||||
chr16:1782506-1783015 | Common:4; Rare:169 | ||||
chr16:1826790-1826970 | Common:3; Rare:57 | ||||
chr16:1943116-1943490 | Common:1; Rare:118 | ||||
chr16:1964814-1965061 | Common:6; Rare:111 | ||||
chr16:1971927-1972123 | Common:1; Rare:56 | ||||
chr16:2047724-2048043 | Rare:155; Clinvar:2; Clinvar (benign):1 | ||||
chr16:2268072-2268172 | Rare:46 | ||||
chr16:2459886-2460136 | Rare:79 | ||||
chr16:2474994-2475160 | Rare:55; Clinvar (benign):2 | ||||
chr16:2537697-2538063 | Common:4; Rare:138 | ||||
chr16:2682415-2682543 | Rare:59 |