| ID: 129999946 | ATAC-STARR-seq lymphoblastoid active region 27057 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (19408489..19408548) | | |
| ID: 129999945 | ATAC-STARR-seq lymphoblastoid active region 27056 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (19386008..19386097) | | |
| ID: 129999944 | ATAC-STARR-seq lymphoblastoid active region 27055 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (19385888..19385987) | | |
| ID: 129662245 | ReSE screen-validated silencer GRCh37_chr8:19230007-19230168 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (19372496..19372657) | | |
| ID: 127458805 | OCT4-NANOG hESC enhancer GRCh37_chr8:19497293-19497837 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (19639782..19640326) | | |
| ID: 127458804 | H3K4me1 hESC enhancer GRCh37_chr8:19263473-19263973 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (19405962..19406462) | | |
| ID: 127458803 | H3K4me1 hESC enhancer GRCh37_chr8:19262972-19263472 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (19405461..19405961) | | |
| ID: 126860315 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr8:19435762-19436961 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (19578251..19579450) | | |
| ID: 126860314 | MED14-independent group 3 enhancer GRCh37_chr8:19394183-19395382 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (19536672..19537871) | | |
| ID: 124901900 | uncharacterized LOC124901900 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (19641151..19650586) | | |
| ID: 105379306 | uncharacterized LOC105379306 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (19300523..19311824) | | |
| ID: 105379300 | uncharacterized LOC105379300 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (19246056..19277381) | | |
| ID: 100128993 | uncharacterized LOC100128993 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (19183674..19245522, complement) | | |
| ID: 442382 | ATPase plasma membrane Ca2+ transporting 1 pseudogene [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (19238437..19240873) | | |
| ID: 63898 | SH2 domain containing 4A [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (19313693..19396218) | PPP1R38, SH2A | 614968 |
| ID: 55790 | chondroitin sulfate N-acetylgalactosaminyltransferase 1 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (19404161..19757908, complement) | CSGalNAcT-1, ChGn, ChGn-1, SDJLABA, beta4GalNAcT | 616615 |