ID: 129664198 | ReSE screen-validated silencer GRCh37_chr18:7043747-7043948 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (7043748..7043949) | | |
ID: 127888716 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr18:7203119-7203796 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (7203121..7203798) | | |
ID: 127888715 | H3K4me1 hESC enhancer GRCh37_chr18:7158211-7158711 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (7158212..7158712) | | |
ID: 127888714 | H3K4me1 hESC enhancer GRCh37_chr18:6951323-6951880 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (6951324..6951881) | | |
ID: 126862686 | MED14-independent group 3 enhancer GRCh37_chr18:7034687-7035886 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (7034688..7035887) | | |
ID: 126862685 | BRD4-independent group 4 enhancer GRCh37_chr18:6958646-6959845 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (6958647..6959846) | | |
ID: 112543434 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr18:7038146-7039345 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (7038101..7039346) | | |
ID: 106481468 | RNA, U6 small nuclear 916, pseudogene [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (6936912..6937020, complement) | | |
ID: 101927188 | uncharacterized LOC101927188 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (6954677..6957419) | | |
ID: 100421167 | SCML2 pseudogene 1 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (6926974..6928215) | | |
ID: 645423 | SLC25A51 pseudogene 2 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (7134120..7135875) | MCART4P | |
ID: 400643 | long intergenic non-protein coding RNA 668 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (6925474..6929869, complement) | | |
ID: 339291 | leucine rich repeat containing 30 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (7231089..7232044) | | |
ID: 284217 | laminin subunit alpha 1 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (6941742..7117797, complement) | LAMA, PTBHS, S-LAM-alpha | 150320 |