Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:2033060-2033343 | Common:1; Rare:68 | ||||
chr16:2047231-2047460 | Rare:56 | ||||
chr16:2047768-2048058 | Rare:145; Clinvar:2; Clinvar (benign):5 | ||||
chr16:2205673-2205894 | Common:4; Rare:102 | ||||
chr16:2207078-2207226 | Common:1; Rare:57 | ||||
chr16:2223309-2223661 | Rare:143 | ||||
chr16:2267780-2267887 | Rare:38 | ||||
chr16:2268053-2268520 | Common:5; Rare:169 | ||||
chr16:2429148-2429472 | Common:2; Rare:106 | ||||
chr16:2459940-2460147 | Common:1; Rare:61 | ||||
chr16:2474976-2475151 | Rare:55 | ||||
chr16:2513635-2514054 | Rare:158 | ||||
chr16:2514083-2514179 | Common:1; Rare:28 | ||||
chr16:2520253-2520436 | Common:5; Rare:113 | ||||
chr16:2537697-2538136 | Common:4; Rare:164 |