| ID: 127893958 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:57276557-57277089 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (58701501..58702033) | | |
| ID: 127893957 | H3K4me1 hESC enhancer GRCh37_chr20:57269435-57270042 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (58694379..58694986) | | |
| ID: 127893956 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:57267289-57267994 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (58692233..58692938) | | |
| ID: 127893955 | H3K4me1 hESC enhancer GRCh37_chr20:57251409-57251933 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (58676353..58676877) | | |
| ID: 127893954 | H3K4me1 hESC enhancer GRCh37_chr20:57250883-57251408 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (58675827..58676352) | | |
| ID: 127893953 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:57245701-57246356 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (58670645..58671300) | | |
| ID: 127893952 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:57245043-57245700 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (58669987..58670644) | | |
| ID: 127893951 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:57244387-57245042 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (58669331..58669986) | | |
| ID: 127893950 | H3K27ac hESC enhancer GRCh37_chr20:57236323-57236822 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (58661267..58661766) | | |
| ID: 127893949 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr20:57227205-57227708 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (58652042..58652652) | | |
| ID: 127893948 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:57223531-57224068 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (58648475..58649012) | | |
| ID: 125387311 | Sharpr-MPRA regulatory region 5631 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (58647493..58647787) | | |
| ID: 107985410 | uncharacterized LOC107985410 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (58640123..58649635, complement) | | |
| ID: 100534593 | STX16-NPEPL1 readthrough (NMD candidate) [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (58651253..58715844) | | |
| ID: 79716 | aminopeptidase like 1 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (58689131..58715844) | bA261P9.2 | |
| ID: 8675 | syntaxin 16 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (58651283..58679526) | SYN-16, SYN16 | 603666 |