ID: 127889981 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:2476197-2476784 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (2476199..2476786) | | |
ID: 127889980 | H3K4me1 hESC enhancer GRCh37_chr19:2454977-2455685 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (2454979..2455687) | | |
ID: 127889979 | H3K4me1 hESC enhancer GRCh37_chr19:2454266-2454976 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (2454268..2454978) | | |
ID: 127889978 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:2453595-2454209 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (2453597..2454211) | | |
ID: 127889977 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:2452980-2453594 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (2452982..2453596) | | |
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: 127617022 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:2426331-2427074 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (2426333..2427076) | | |
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: 101928602 | long intergenic non-protein coding RNA 1775 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (2458937..2462185, complement) | | |
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 |
ID: 4616 | growth arrest and DNA damage inducible beta [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (2476127..2478257) | GADD45BETA, MYD118 | 604948 |