| ID: 129935047 | ATAC-STARR-seq lymphoblastoid active region 16729 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (165898024..165898113) | | |
| ID: 129935046 | ATAC-STARR-seq lymphoblastoid active region 16728 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (165874554..165874753) | | |
| ID: 127275159 | NANOG-H3K27ac hESC enhancer GRCh37_chr2:166810301-166811050 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (165953627..165954540) | | |
| ID: 127275158 | H3K27ac hESC enhancer GRCh37_chr2:166710405-166710906 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (165853895..165854396) | | |
| ID: 127275157 | NANOG hESC enhancer GRCh37_chr2:166700603-166701418 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (165844093..165844908) | | |
| ID: 127275156 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:166650414-166651319 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (165793880..165794809) | | |
| ID: 127275155 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:166649507-166650413 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (165792997..165793903) | | |
| ID: 124906086 | uncharacterized LOC124906086 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (165793586..165803756) | | |
| ID: 106479163 | RN7SK pseudogene 152 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (166180652..166180966, complement) | | |
| ID: 102724058 | uncharacterized LOC102724058 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (165957418..166036400) | | |
| ID: 101929680 | SCN1A and SCN9A antisense RNA 1 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (166081531..166301784) | SCN1A-NAT, SCN1ANAT | |
| ID: 100506134 | TTC21B antisense RNA 1 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (165933857..165948321) | | |
| ID: 100506124 | uncharacterized LOC100506124 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (165857475..165871941, complement) | | |
| ID: 79809 | tetratricopeptide repeat domain 21B [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (165873362..165953776, complement) | ATD4, CFAP60, FAP60, FLA17, IFT139, IFT139B, JBTS11, NPHP12, Nbla10696, SRTD4, THM1 | 612014 |
| ID: 6323 | sodium voltage-gated channel alpha subunit 1 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (165984641..166149161, complement) | DEE6, DEE6A, DEE6B, DRVT, EIEE6, FEB3, FEB3A, FHM3, GEFSP2, HBSCI, NAC1, Nav1.1, SCN1, SMEI | 182389 |
| ID: 2591 | polypeptide N-acetylgalactosaminyltransferase 3 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (165747588..165794692, complement) | GalNAc-T3, HFTC, HFTC1, HHS | 601756 |