ID: 127889976 | H3K4me1 hESC enhancer GRCh37_chr19:2441645-2442144 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (2441647..2442146) | | |
ID: 127889975 | H3K4me1 hESC enhancer GRCh37_chr19:2441143-2441644 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (2441145..2441646) | | |
ID: 127889974 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:2433582-2434270 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (2433584..2434272) | | |
ID: 127617023 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:2427075-2427820 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (2427077..2427822) | | |
ID: 106804547 | origin of replication adjacent to lamin B2 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (2426874..2428373) | | |
ID: 102466806 | microRNA 7108 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (2434914..2435000, complement) | hsa-mir-7108 | |
ID: 84823 | lamin B2 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (2428166..2456959, complement) | EPM9, LAMB2, LMN2, MCPH27 | 150341 |
ID: 26517 | translocase of inner mitochondrial membrane 13 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (2425625..2427586, complement) | TIM13, TIM13BA, TIMM13B, ppv1, TIMM13 | 607383 |