| ID: 127891792 | NANOG hESC enhancer GRCh37_chr19:46673889-46674439 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (46170632..46171182) | | |
| ID: 127891791 | H3K27ac hESC enhancer GRCh37_chr19:46637729-46638559 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (46134472..46135302) | | |
| ID: 127891790 | NANOG-H3K27ac hESC enhancer GRCh37_chr19:46636897-46637728 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (46133640..46134471) | | |
| ID: 127891789 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:46636065-46636896 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (46132808..46133639) | | |
| ID: 126862914 | BRD4-independent group 4 enhancer GRCh37_chr19:46662347-46663546 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (46159090..46160289) | | |
| ID: 105372424 | uncharacterized LOC105372424 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (46162541..46180879, complement) | | |
| ID: 100533846 | solute carrier family 30 member 5 pseudogene [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (46113205..46113858, complement) | | |
| ID: 388555 | IGF like family member 3 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (46120067..46124688, complement) | UNQ483 | 610546 |
| ID: 147920 | IGF like family member 2 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (46078513..46215362) | UNQ645, VPRI645 | 610545 |
| ID: 126052 | TGFB induced factor homeobox 1 pseudogene 1 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (46136282..46137597, complement) | | |