ID: 127402141 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr4:190767907-190768620 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (189846752..189847465) | | |
ID: 127402140 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr4:190767193-190767906 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (189846038..189846751) | | |
ID: 127402139 | H3K4me1 hESC enhancer GRCh37_chr4:190749823-190750323 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (189828668..189829168) | | |
ID: 127402138 | H3K4me1 hESC enhancer GRCh37_chr4:190749322-190749822 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (189828168..189828667) | | |
ID: 127402137 | NANOG-H3K27ac hESC enhancer GRCh37_chr4:190405973-190406728 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (189484819..189485574) | | |
ID: 127402136 | H3K27ac hESC enhancer GRCh37_chr4:190405217-190405972 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (189484063..189484818) | | |
ID: 127402135 | OCT4-NANOG hESC enhancer GRCh37_chr4:190400698-190401256 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (189479544..189480102) | | |
ID: 126807279 | BRD4-independent group 4 enhancer GRCh37_chr4:190802184-190803383 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (189880899..189882228) | | |
ID: 126807276 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr4:190523074-190524273 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (189601920..189603119) | | |
ID: 126807275 | BRD4-independent group 4 enhancer GRCh37_chr4:190471799-190472998 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (189550645..189551844) | | |
ID: 126088085 | BRD4-independent group 4 enhancer GRCh37_chr4:190615457-190616656 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (189694303..189695502) | | |
ID: 107987311 | uncharacterized LOC107987311 [Homo sapiens (human)] | | | |
ID: 106480163 | RNA, U1 small nuclear 51, pseudogene [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (189709539..189709714, complement) | | |
ID: 105377619 | uncharacterized LOC105377619 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (189814945..189820145) | | |
ID: 105377617 | long intergenic non-protein coding RNA 1596 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (189881515..189884868) | | |
ID: 105377616 | uncharacterized LOC105377616 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (189703880..189723158, complement) | | |
ID: 105377615 | uncharacterized LOC105377615 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (189550782..189552089) | | |
ID: 105377614 | uncharacterized LOC105377614 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (189364340..189391702) | | |
ID: 101928971 | long intergenic non-protein coding RNA 1262 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (189659606..189661486) | TCONS_l2_00021807 | |
ID: 728339 | FRG1 divergent transcript [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (189764391..189940733, complement) | | |