| ID: 126806393 | MED14-independent group 3 enhancer GRCh37_chr2:163175227-163176426 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (162318599..162319916) | | |
| ID: 124906084 | uncharacterized LOC124906084 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (162490334..162499045) | | |
| ID: 105373724 | uncharacterized LOC105373724 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (162246117..162261156) | | |
| ID: 101929532 | uncharacterized LOC101929532 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (162114441..162172739) | | |
| ID: 100873379 | RNA, 5S ribosomal pseudogene 109 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (162496936..162497051) | RN5S109 | |
| ID: 90134 | potassium voltage-gated channel subfamily H member 7 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (162371407..162838767, complement) | ERG3, HERG3, Kv11.3 | 608169 |
| ID: 64135 | interferon induced with helicase C domain 1 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (162267074..162318684, complement) | AGS7, Hlcd, IDDM19, IMD95, MDA-5, MDA5, RLR-2, SGMRT1 | 606951 |
| ID: 25801 | grancalcin [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (162318763..162375396) | GCL | 607030 |
| ID: 2191 | fibroblast activation protein alpha [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (162170684..162243445, complement) | DPPIVA, FAPalpha, SIMP, FAP | 600403 |