| ID: 129660901 | ReSE screen-validated silencer GRCh37_chr2:219290512-219290729 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (218425789..218426006) | | |
| ID: 127275778 | H3K27ac hESC enhancer GRCh37_chr2:219442335-219442835 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (218577612..218578112) | | |
| ID: 127275777 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:219433545-219434172 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (218568822..218569449) | | |
| ID: 127275776 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:219432917-219433544 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (218568194..218568821) | | |
| ID: 127275775 | NANOG hESC enhancer GRCh37_chr2:219366267-219366838 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (218501544..218502115) | | |
| ID: 127275774 | H3K4me1 hESC enhancer GRCh37_chr2:219289129-219289629 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (218424406..218424906) | | |
| ID: 124906133 | uncharacterized LOC124906133 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (218619801..218619887) | | |
| ID: 122861291 | Sharpr-MPRA regulatory region 3568 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (218466126..218466420) | | |
| ID: 106479626 | RNA, U6 small nuclear 136, pseudogene [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (218589214..218589320, complement) | | |
| ID: 106479112 | RN7SK pseudogene 38 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (218500729..218501037, complement) | | |
| ID: 100189503 | tRNA-Gln (anticodon CTG) 16-1 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (218626409..218626484) | TRNAQ44P | |
| ID: 84812 | phospholipase C delta 4 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (218607899..218637175) | | 605939 |
| ID: 57695 | ubiquitin specific peptidase 37 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (218450251..218568351, complement) | | 620226 |
| ID: 9125 | CCR4-NOT transcription complex subunit 9 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (218568839..218597080) | CAF40, CT129, RCD-1, RCD1, RQCD1 | 612054 |
| ID: 7429 | villin 1 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (218419123..218453295) | D2S1471, VIL | 193040 |