| ID: 130055471 | ATAC-STARR-seq lymphoblastoid silent region 5664 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (34498969..34499068) | | |
| ID: 129663419 | ReSE screen-validated silencer GRCh37_chr14:35022516-35022692 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (34553310..34553486) | | |
| ID: 127827373 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr14:35024749-35025306 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (34555543..34556100) | | |
| ID: 127827372 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr14:35016231-35016802 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (34547025..34547596) | | |
| ID: 127827371 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr14:35008110-35009034 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (34538904..34539878) | | |
| ID: 127827370 | H3K27ac hESC enhancer GRCh37_chr14:34964993-34965682 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (34495787..34496476) | | |
| ID: 126861915 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr14:34965742-34966941 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (34496477..34497735) | | |
| ID: 124995366 | Sharpr-MPRA regulatory region 9667 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (34537543..34537837) | | |
| ID: 112268123 | uncharacterized LOC112268123 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (34541234..34543454, complement) | | |
| ID: 106799849 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr14:35025307-35025864 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (34556101..34556658) | | |
| ID: 106799848 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr14:35015659-35016230 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (34546453..34547024) | | |
| ID: 105370449 | uncharacterized LOC105370449 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (34544089..34557252, complement) | | |
| ID: 105370447 | uncharacterized LOC105370447 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (34539749..34541706) | | |
| ID: 728953 | ribosomal protein S19 pseudogene 3 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (34568617..34569169, complement) | RPS19_4_1350 | |
| ID: 644384 | ribosomal protein L23a pseudogene 71 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (34485966..34486492) | RPL23A_33_1349 | |
| ID: 58533 | sorting nexin 6 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (34561093..34630148, complement) | MSTP010, TFAF2 | 606098 |
| ID: 55837 | E2F associated phosphoprotein [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (34515938..34539701, complement) | BM036, C14orf11 | 609486 |
| ID: 26866 | RNA, U1 small nuclear 28, pseudogene [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (34556226..34556389, complement) | RNU1-8, RNU1-8P | |
| ID: 26865 | RNA, U1 small nuclear 27, pseudogene [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (34546714..34546877) | RNU1-7, RNU1-7P | |