| ID: 130064906 | ATAC-STARR-seq lymphoblastoid active region 14929 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49232014..49232093) | | |
| ID: 130064905 | ATAC-STARR-seq lymphoblastoid active region 14928 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49226079..49226128) | | |
| ID: 130064904 | ATAC-STARR-seq lymphoblastoid active region 14927 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49149523..49149742) | | |
| ID: 130064903 | ATAC-STARR-seq lymphoblastoid silent region 10914 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49127873..49128272) | | |
| ID: 129664498 | ReSE screen-validated silencer GRCh37_chr19:49700016-49700342 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49196759..49197085) | | |
| ID: 129664497 | ReSE screen-validated silencer GRCh37_chr19:49662088-49662274 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49158831..49159017) | | |
| ID: 127891979 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:49713888-49714526 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49210631..49211269) | | |
| ID: 127891978 | H3K4me1 hESC enhancer GRCh37_chr19:49692147-49692646 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49188890..49189389) | | |
| ID: 127891977 | H3K4me1 hESC enhancer GRCh37_chr19:49691645-49692146 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49188388..49188889) | | |
| ID: 127891976 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:49669228-49669870 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49165971..49166613) | | |
| ID: 127891975 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:49668584-49669227 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49165327..49165970) | | |
| ID: 127891974 | H3K4me1 hESC enhancer GRCh37_chr19:49660783-49661404 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49157526..49158147) | | |
| ID: 127891973 | H3K4me1 hESC enhancer GRCh37_chr19:49654589-49655198 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49151332..49151941) | | |
| 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: 107985340 | uncharacterized LOC107985340 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49221844..49269496) | | |
| ID: 101290502 | SUMO1 pseudogene 4 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49275026..49276499) | | |
| ID: 652969 | solute carrier family 6 member 21, pseudogene [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49252333..49256340, complement) | SLC6A21 | |