| ID: 132090549 | Neanderthal introgressed variant-containing enhancer experimental_51262 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (34100186..34100355) | | |
| ID: 130064189 | ATAC-STARR-seq lymphoblastoid silent region 10501 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (34134359..34134768) | | |
| ID: 129391093 | MPRA-validated peak3442 silencer [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (34259175..34259375) | | |
| ID: 129391092 | MPRA-validated peak3441 silencer [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (34236031..34236231) | | |
| ID: 127891251 | H3K4me1 hESC enhancer GRCh37_chr19:34857175-34857915 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (34366270..34367010) | | |
| ID: 127891250 | H3K27ac hESC enhancer GRCh37_chr19:34850825-34851431 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (34359920..34360526) | | |
| ID: 127891249 | H3K4me1 hESC enhancer GRCh37_chr19:34833051-34833551 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (34342146..34342646) | | |
| ID: 127891248 | H3K4me1 hESC enhancer GRCh37_chr19:34801395-34801894 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (34310490..34310989) | | |
| ID: 127891247 | H3K27ac hESC enhancer GRCh37_chr19:34761021-34761721 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (34270116..34270816) | | |
| ID: 127891246 | H3K27ac hESC enhancer GRCh37_chr19:34745756-34746277 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (34254851..34255372) | | |
| ID: 127891245 | NANOG-H3K27ac hESC enhancer GRCh37_chr19:34728773-34729345 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (34237868..34238440) | | |
| ID: 127891244 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr19:34715679-34716244 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (34224774..34225339) | | |
| ID: 127891243 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:34625657-34626192 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (34134752..34135287) | | |
| ID: 127891242 | H3K4me1 hESC enhancer GRCh37_chr19:34617551-34618060 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (34126646..34127155) | | |
| ID: 112543484 | Sharpr-MPRA regulatory region 14193 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (34319784..34320078) | | |
| ID: 100128110 | coiled-coil-helix-coiled-coil-helix domain containing 2 pseudogene 3 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (34126925..34127713) | | |
| ID: 401911 | ribosomal protein L29 pseudogene 33 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (34296163..34296784, complement) | RPL29_22_1650 | |
| ID: 126235 | ribosomal protein S4X pseudogene 21 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (34092476..34093361, complement) | RPS4P21, RPS4X_10_1649 | |
| ID: 26065 | LSM14A mRNA processing body assembly factor [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (34172504..34229288) | C19orf13, FAM61A, RAP55, RAP55A | 610677 |
| ID: 9710 | granule associated Rac and RHOG effector 1 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (34254554..34355566) | KIAA0355, MiniBAR | 619335 |