| ID: 130056234 | ATAC-STARR-seq lymphoblastoid active region 8844 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (88824303..88824662) | | |
| ID: 130056233 | ATAC-STARR-seq lymphoblastoid silent region 5994 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (88792734..88793093) | | |
| ID: 130056232 | ATAC-STARR-seq lymphoblastoid silent region 5993 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (88792464..88792543) | | |
| ID: 130056231 | ATAC-STARR-seq lymphoblastoid active region 8843 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (88668395..88668574) | | |
| ID: 130056230 | ATAC-STARR-seq lymphoblastoid active region 8842 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (88600052..88600331) | | |
| ID: 130056229 | ATAC-STARR-seq lymphoblastoid silent region 5992 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (88562826..88563535) | | |
| ID: 130056228 | ATAC-STARR-seq lymphoblastoid silent region 5991 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (88554965..88555014) | | |
| ID: 130056227 | ATAC-STARR-seq lymphoblastoid active region 8841 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (88492443..88492632) | | |
| ID: 130056226 | ATAC-STARR-seq lymphoblastoid active region 8840 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (88385530..88385849) | | |
| ID: 129390658 | MPRA-validated peak2226 silencer [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (88766312..88766512) | | |
| ID: 127828190 | OCT4-NANOG hESC enhancer GRCh37_chr14:89084698-89085319 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (88618354..88618975) | | |
| ID: 127828189 | H3K4me1 hESC enhancer GRCh37_chr14:89015655-89016472 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (88549311..88550128) | | |
| ID: 127828188 | NANOG hESC enhancer GRCh37_chr14:88948745-88949275 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (88482401..88482931) | | |
| ID: 124903405 | proline-rich protein 2-like [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (88554657..88556790, complement) | | |
| ID: 107057646 | RNA, U4 small nuclear 22, pseudogene [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (88513498..88513663) | | |
| ID: 106479601 | RNA, U4 small nuclear 92, pseudogene [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (88820297..88820432) | | |
| ID: 105370614 | uncharacterized LOC105370614 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (88500867..88515502) | | |
| ID: 161436 | EMAP like 5 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (88612431..88792953, complement) | EMAP-2, EMAP-5, FAP16 | 618119 |
| ID: 123016 | tetratricopeptide repeat domain 8 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (88824153..88881079) | BBS8, RP51 | 608132 |
| ID: 79882 | zinc finger CCCH-type containing 14 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (88563037..88627596) | MRT56, MSUT-2, NY-REN-37, SUT2, UKp68 | 613279 |