ID: 129662849 | ReSE screen-validated silencer GRCh37_chr11:2135598-2135868 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (2114368..2114638) | | |
ID: 127820162 | OCT4-NANOG hESC enhancer GRCh37_chr11:2244593-2245167 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (2223363..2223937) | | |
ID: 127820161 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr11:2235935-2236495 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (2214705..2215265) | | |
ID: 127820160 | H3K4me1 hESC enhancer GRCh37_chr11:2233643-2234213 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (2212413..2212983) | | |
ID: 127820159 | H3K4me1 hESC enhancer GRCh37_chr11:2225905-2226503 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (2204675..2205273) | | |
ID: 127820158 | H3K4me1 hESC enhancer GRCh37_chr11:2198066-2198912 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (2176836..2177682) | | |
ID: 127820157 | H3K4me1 hESC enhancer GRCh37_chr11:2158413-2159034 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (2137183..2137804) | | |
ID: 127820156 | H3K4me1 hESC enhancer GRCh37_chr11:2155593-2156179 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (2134363..2134949) | | |
ID: 127820155 | H3K4me1 hESC enhancer GRCh37_chr11:2148496-2149320 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (2127266..2128090) | | |
ID: 127820154 | H3K4me1 hESC enhancer GRCh37_chr11:2121704-2122345 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (2100474..2101115) | | |
ID: 127820153 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr11:2121061-2121703 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (2099831..2100473) | | |
ID: 127820152 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr11:2118490-2119132 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (2097260..2097902) | | |
ID: 109623489 | insulin repeat instability region [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (2161574..2161971) | | |
ID: 100616126 | microRNA 4686 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (2173063..2173138) | | |
ID: 723961 | INS-IGF2 readthrough [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (2129117..2161209, complement) | INSIGF | |
ID: 619552 | microRNA 483 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (2134134..2134209, complement) | MIRN483, hsa-mir-483, mir-483 | |
ID: 51214 | IGF2 antisense RNA [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (2140512..2148666) | IGF2-AS1, IGF2AS, PEG8 | 610146 |
ID: 7054 | tyrosine hydroxylase [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (2163929..2171815, complement) | DYT14, DYT5b, TYH | 191290 |
ID: 3630 | insulin [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (2159779..2161209, complement) | IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10, PNDM4 | 176730 |
ID: 3481 | insulin like growth factor 2 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (2129117..2149566, complement) | C11orf43, GRDF, IGF-II, PP9974, SRS3 | 147470 |