Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:1771505-1771630 | Rare:52 | ||||
chr16:1782508-1783009 | Common:4; Rare:166 | ||||
chr16:1943152-1943497 | Common:1; Rare:107 | ||||
chr16:1964824-1965003 | Common:6; Rare:75 | ||||
chr16:1971932-1972113 | Common:1; Rare:52 | ||||
chr16:2047804-2048058 | Rare:127; Clinvar:2; Clinvar (benign):5 | ||||
chr16:2155348-2155514 | Rare:51 | ||||
chr16:2268063-2268198 | Common:1; Rare:62 | ||||
chr16:2429156-2429472 | Common:2; Rare:99 | ||||
chr16:2459940-2460133 | Rare:52 | ||||
chr16:2682350-2682628 | Rare:131 | ||||
chr16:2770150-2770387 | Common:1; Rare:71 | ||||
chr16:2777235-2777380 | Common:1; Rare:58 | ||||
chr16:3065195-3065432 | Common:3; Rare:63 | ||||
chr16:3112490-3112628 | Common:2; Rare:33 |