| ID: 130064747 | ATAC-STARR-seq lymphoblastoid silent region 10808 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (46016863..46016922) | | |
| ID: 130064746 | ATAC-STARR-seq lymphoblastoid silent region 10807 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (46016053..46016132) | | |
| 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: 127891788 | H3K4me1 hESC enhancer GRCh37_chr19:46535831-46536434 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (46032573..46033176) | | |
| ID: 127891787 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:46524919-46525804 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (46021661..46022546) | | |
| ID: 126862914 | BRD4-independent group 4 enhancer GRCh37_chr19:46662347-46663546 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (46159090..46160289) | | |
| ID: 125371533 | Sharpr-MPRA regulatory region 13926 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (46015291..46015585) | | |
| ID: 105372424 | uncharacterized LOC105372424 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (46162541..46180879, complement) | | |
| ID: 105372421 | uncharacterized LOC105372421 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (46027811..46029914) | | |
| ID: 100533846 | solute carrier family 30 member 5 pseudogene [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (46113205..46113858, complement) | | |
| ID: 768217 | microRNA 769 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (46018932..46019049) | MIRN769, hsa-mir-769, mir-769 | |
| ID: 729440 | coiled-coil domain containing 61 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (45995467..46018616) | VFL3, hVFL3 | 620676 |
| ID: 444882 | IGF like family member 4 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (46039182..46077629, complement) | | 610547 |
| 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) | | |
| ID: 8993 | peptidoglycan recognition protein 1 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (46019153..46023053, complement) | PGLYRP, PGRP, PGRP-S, PGRPS, TAG7, TNFSF3L | 604963 |