ID: 127894639 | H3K4me1 hESC enhancer GRCh37_chr21:38655347-38656273 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (37283045..37283971) | | |
ID: 127894638 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr21:38630368-38630960 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (37258067..37258659) | | |
ID: 127894637 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr21:38629775-38630367 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (37257474..37258078) | | |
ID: 127894636 | H3K4me1 hESC enhancer GRCh37_chr21:38579468-38580304 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (37207167..37208003) | | |
ID: 124905019 | uncharacterized LOC124905019 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (37341405..37344214, complement) | | |
ID: 124905018 | uncharacterized LOC124905018 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (37293661..37296532) | | |
ID: 106481108 | RNA, 7SL, cytoplasmic 678, pseudogene [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (37215605..37215903) | | |
ID: 257203 | Down syndrome critical region 9 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (37208503..37221736) | NCRNA00038 | |
ID: 10311 | VPS26 endosomal protein sorting factor C [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (37223420..37268108, complement) | DCRA, DSCR3, DSCRA | 605298 |