| ID: 128772328 | melanoma risk locus-associated MPRA allelic enhancer 8:22014424 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22156839..22156983) | | |
| ID: 127458872 | H3K4me1 hESC enhancer GRCh37_chr8:22077527-22078227 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22220014..22220714) | | |
| ID: 127458871 | H3K4me1 hESC enhancer GRCh37_chr8:22071895-22072757 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22214382..22215244) | | |
| ID: 127458870 | H3K4me1 hESC enhancer GRCh37_chr8:22069059-22069750 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22211546..22212237) | | |
| ID: 127458869 | H3K4me1 hESC enhancer GRCh37_chr8:22068368-22069058 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22210855..22211545) | | |
| ID: 127458868 | H3K4me1 hESC enhancer GRCh37_chr8:22067676-22068367 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22210163..22210854) | | |
| ID: 127458867 | H3K4me1 hESC enhancer GRCh37_chr8:22054519-22055286 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22197006..22197773) | | |
| ID: 127458866 | H3K4me1 hESC enhancer GRCh37_chr8:22046165-22046665 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22188652..22189152) | | |
| ID: 127458865 | H3K27ac hESC enhancer GRCh37_chr8:22031123-22031622 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22173610..22174109) | | |
| ID: 126860323 | BRD4-independent group 4 enhancer GRCh37_chr8:22048316-22049515 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22190803..22192002) | | |
| ID: 124901904 | uncharacterized LOC124901904 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22187776..22191595, complement) | | |
| ID: 113788269 | BRD4-independent group 4 enhancer GRCh37_chr8:22052064-22053263 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22194376..22195750) | | |
| ID: 9796 | phytanoyl-CoA 2-hydroxylase interacting protein [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22219703..22232099, complement) | DYRK1AP3, PAHX-AP, PAHXAP1 | 608511 |
| ID: 6440 | surfactant protein C [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22157383..22164479) | BRICD6, PSP-C, SFTP2, SMDP2, SP-C, SP5 | 178620 |
| ID: 649 | bone morphogenetic protein 1 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22165372..22212326) | OI13, PCOLC, PCP, PCP2, TLD | 112264 |