| ID: 132089582 | Neanderthal introgressed variant-containing enhancer experimental_102343 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (16868484..16868653) | | |
| ID: 129999929 | ATAC-STARR-seq lymphoblastoid silent region 18960 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (17155941..17157300) | | |
| ID: 129999928 | ATAC-STARR-seq lymphoblastoid active region 27046 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (17027776..17027865) | | |
| ID: 129999927 | ATAC-STARR-seq lymphoblastoid silent region 18959 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (17027216..17027625) | | |
| ID: 129999926 | ATAC-STARR-seq lymphoblastoid silent region 18958 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (17001862..17001931) | | |
| ID: 127458776 | NANOG hESC enhancer GRCh37_chr8:16918455-16918956 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (17060946..17061447) | | |
| ID: 127458775 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr8:16801751-16802334 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (16944242..16944825) | | |
| ID: 127458774 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr8:16801165-16801750 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (16943656..16944241) | | |
| ID: 107986918 | uncharacterized LOC107986918 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (17162776..17164847) | | |
| ID: 106481052 | RNA, 7SL, cytoplasmic 474, pseudogene [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (16863196..16863496, complement) | | |
| ID: 105379297 | uncharacterized LOC105379297 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (16783215..16916072, complement) | | |
| ID: 100130392 | ribosomal protein L9 pseudogene 20 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (17150203..17150909, complement) | RPL9_7_879 | |
| ID: 286097 | mitochondrial calcium uptake family member 3 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (17027238..17138640) | EFHA2, hMICU3 | 610633 |
| ID: 51201 | zinc finger DHHC-type palmitoyltransferase 2 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (17156482..17224799) | DHHC2, ZNF372 | 618621 |
| ID: 26281 | fibroblast growth factor 20 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (16992181..17002345, complement) | FGF-20, RHDA2 | 605558 |