ID: 127891972 | H3K4me1 hESC enhancer GRCh37_chr19:49644909-49645502 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49141652..49142245) | | |
ID: 127891971 | H3K4me1 hESC enhancer GRCh37_chr19:49640079-49640585 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49136822..49137328) | | |
ID: 127891970 | H3K4me1 hESC enhancer GRCh37_chr19:49635887-49636531 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49132630..49133274) | | |
ID: 127891969 | H3K4me1 hESC enhancer GRCh37_chr19:49623585-49624085 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49120328..49120828) | | |
ID: 127891968 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:49621711-49622222 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49118454..49118965) | | |
ID: 127891967 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:49610053-49610894 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49106796..49107637) | | |
ID: 127891966 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:49604029-49604882 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49100772..49101625) | | |
ID: 127891965 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:49603173-49604028 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49099916..49100771) | | |
ID: 127891964 | H3K4me1 hESC enhancer GRCh37_chr19:49575349-49575848 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49072092..49072591) | | |
ID: 127891963 | H3K4me1 hESC enhancer GRCh37_chr19:49574847-49575348 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49071590..49072091) | | |
ID: 127891962 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:49559434-49560286 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49056177..49057029) | | |
ID: 127891961 | H3K4me1 hESC enhancer GRCh37_chr19:49558580-49559433 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49055323..49056176) | | |
ID: 127891960 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:49557355-49557905 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49054098..49054648) | | |
ID: 127891959 | H3K4me1 hESC enhancer GRCh37_chr19:49546952-49547460 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49043695..49044203) | | |
ID: 127891958 | H3K4me1 hESC enhancer GRCh37_chr19:49546442-49546951 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49043185..49043694) | | |
ID: 127891957 | H3K4me1 hESC enhancer GRCh37_chr19:49512697-49513198 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49009440..49009941) | | |
ID: 127891956 | H3K4me1 hESC enhancer GRCh37_chr19:49507585-49508084 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49004328..49004827) | | |
ID: 124904739 | uncharacterized LOC124904739 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49055417..49059836, complement) | | |
ID: 124904738 | uncharacterized LOC124904738 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49020093..49022815) | | |
ID: 121627885 | Sharpr-MPRA regulatory region 164 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49017812..49018839) | | |