| ID: 127893366 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:41804429-41805039 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (43175789..43176399) | | |
| ID: 127893365 | H3K4me1 hESC enhancer GRCh37_chr20:41733081-41733580 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (43104441..43104940) | | |
| ID: 127893364 | OCT4-NANOG hESC enhancer GRCh37_chr20:40937504-40938187 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (42308864..42309547) | | |
| ID: 127893363 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:40834580-40835212 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (42205940..42206572) | | |
| ID: 127893362 | H3K4me1 hESC enhancer GRCh37_chr20:40627259-40627760 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (41998619..41999120) | | |
| ID: 126863032 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr20:41379572-41380771 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (42750932..42752131) | | |
| ID: 125387274 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr20:41614665-41615864 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (42986025..42987224) | | |
| ID: 124904981 | uncharacterized LOC124904981 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (42826554..42826702) | | |
| ID: 121853075 | PTPRT divergent transcript [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (43190065..43202599) | | |
| ID: 106481854 | RNA, 7SL, cytoplasmic 666, pseudogene [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (43222206..43222509) | | |
| ID: 106479139 | RN7SK pseudogene 100 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (43063326..43063609) | | |
| ID: 105372624 | uncharacterized LOC105372624 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (42630843..42647554) | | |
| ID: 105372623 | uncharacterized LOC105372623 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (42949390..42955794) | | |
| ID: 105372622 | uncharacterized LOC105372622 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (42014541..42024127, complement) | | |
| ID: 101927182 | uncharacterized LOC101927182 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (41903848..42108504) | | |
| ID: 101927159 | uncharacterized LOC101927159 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (42685483..42688562) | | |
| ID: 101927138 | PTPRT antisense RNA 1 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (42968743..42971492) | | |
| ID: 643172 | NEFH pseudogene 2 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (41996935..41999447, complement) | | |
| ID: 170536 | peptidylprolyl isomerase A pseudogene 21 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (43230733..43231461) | PPIAL, dJ269M15.1 | |
| ID: 11122 | protein tyrosine phosphatase receptor type T [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (42031890..43189906, complement) | R-PTP-T, RPTP-rho, RPTPrho | 608712 |