ID: 129663717 | ReSE screen-validated silencer GRCh37_chr16:1274120-1274306 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (1224120..1224306) | | |
ID: 127882715 | H3K4me1 hESC enhancer GRCh37_chr16:1289151-1289731 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (1239150..1239730) | | |
ID: 127882714 | H3K4me1 hESC enhancer GRCh37_chr16:1288568-1289150 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (1238567..1239149) | | |
ID: 127882713 | H3K4me1 hESC enhancer GRCh37_chr16:1248579-1249136 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (1198579..1199136) | | |
ID: 127882712 | H3K4me1 hESC enhancer GRCh37_chr16:1248019-1248578 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (1198019..1198578) | | |
ID: 127882711 | H3K4me1 hESC enhancer GRCh37_chr16:1222787-1223288 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (1172787..1173288) | | |
ID: 127882710 | H3K4me1 hESC enhancer GRCh37_chr16:1213358-1213914 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (1163358..1163914) | | |
ID: 127882709 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:1208711-1209430 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (1158711..1159430) | | |
ID: 127882708 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:1203960-1204727 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (1153960..1154727) | | |
ID: 127882707 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:1202005-1202585 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (1152005..1152585) | | |
ID: 127882706 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:1194949-1195763 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (1144949..1145763) | | |
ID: 127882705 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:1194132-1194948 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (1144132..1144948) | | |
ID: 127882704 | H3K4me1 hESC enhancer GRCh37_chr16:1188009-1188509 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (1138009..1138509) | | |
ID: 127882703 | H3K4me1 hESC enhancer GRCh37_chr16:1167285-1167853 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (1117285..1117853) | | |
ID: 127882702 | H3K4me1 hESC enhancer GRCh37_chr16:1157970-1158488 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (1107970..1108488) | | |
ID: 124903623 | uncharacterized LOC124903623 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (1200806..1201711, complement) | | |
ID: 124903622 | uncharacterized LOC124903622 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (1156972..1158610, complement) | | |
ID: 124903621 | uncharacterized LOC124903621 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (1225251..1227240) | | |
ID: 110596865 | 16p subtelomeric meiotic recombination hotspot [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (1125590..1129030) | | |
ID: 110596863 | MS205 minisatellite repeat instability region [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (1184546..1186384) | | |