| ID: 130062846 | ATAC-STARR-seq lymphoblastoid silent region 9621 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (738023..738072) | | |
| ID: 130062845 | ATAC-STARR-seq lymphoblastoid active region 13571 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (734305..734354) | | |
| ID: 130062844 | ATAC-STARR-seq lymphoblastoid silent region 9619 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (703705..704024) | | |
| ID: 130062843 | ATAC-STARR-seq lymphoblastoid silent region 9617 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (680043..680822) | | |
| ID: 130062842 | ATAC-STARR-seq lymphoblastoid silent region 9616 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (679703..680012) | | |
| ID: 127889808 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:782349-782922 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (782349..782922) | | |
| ID: 127889807 | H3K4me1 hESC enhancer GRCh37_chr19:718052-718584 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (718052..718584) | | |
| ID: 127889806 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:707932-708492 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (707932..708492) | | |
| ID: 127889805 | H3K4me1 hESC enhancer GRCh37_chr19:704097-705067 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (704097..705067) | | |
| ID: 127889804 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:681483-682031 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (681483..682031) | | |
| ID: 127889803 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:680933-681482 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (680933..681482) | | |
| ID: 127889802 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:678746-679248 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (678746..679248) | | |
| ID: 125371445 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:778723-779437 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (778723..779437) | | |
| ID: 101928450 | uncharacterized LOC101928450 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (781002..782608, complement) | | |
| ID: 100271250 | ribosomal protein S2 pseudogene 52 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (690442..691211) | RPS2_23_1615 | |
| ID: 400668 | serine protease 57 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (685546..695452, complement) | NSP4, PRSSL1, UNQ782 | |
| ID: 126353 | mitotic spindle positioning [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (748438..764318) | C19orf211, MISP | 615289 |
| ID: 10272 | follistatin like 3 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (676392..683385) | FLRG, FSRP | 605343 |
| ID: 5064 | paralemmin [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (708935..748329) | PALM1 | 608134 |