| ID: 129999943 | ATAC-STARR-seq lymphoblastoid silent region 18968 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (19013757..19013846) | | |
| ID: 129999942 | ATAC-STARR-seq lymphoblastoid silent region 18967 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (19013587..19013686) | | |
| ID: 129662244 | ReSE screen-validated silencer GRCh37_chr8:19068899-19069055 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (19211389..19211545) | | |
| ID: 129662243 | ReSE screen-validated silencer GRCh37_chr8:18859165-18859442 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (19001655..19001932) | | |
| ID: 127458802 | H3K27ac hESC enhancer GRCh37_chr8:19034764-19035693 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (19177254..19178183) | | |
| ID: 127458801 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr8:18942071-18942864 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (19084561..19085354) | | |
| ID: 127458800 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr8:18941277-18942070 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (19083767..19084560) | | |
| ID: 126860313 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr8:19051482-19052681 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (19193972..19195171) | | |
| ID: 124901898 | uncharacterized LOC124901898 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (19014003..19031245) | | |
| ID: 105379306 | uncharacterized LOC105379306 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (19300523..19311824) | | |
| ID: 105379303 | uncharacterized LOC105379303 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (18989262..19006873) | | |
| ID: 105379301 | uncharacterized LOC105379301 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (19091739..19145393) | | |
| 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: 23362 | pleckstrin and Sec7 domain containing 3 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (18527303..19084805, complement) | EFA6D, EFA6R, HCA67 | 614440 |