| ID: 130056277 | ATAC-STARR-seq lymphoblastoid active region 8881 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (90398461..90398760) | | |
| ID: 130056276 | ATAC-STARR-seq lymphoblastoid silent region 6011 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (90398331..90398400) | | |
| ID: 130056275 | ATAC-STARR-seq lymphoblastoid silent region 6010 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (90398221..90398290) | | |
| ID: 130056274 | ATAC-STARR-seq lymphoblastoid silent region 6009 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (90397591..90398140) | | |
| ID: 130056273 | ATAC-STARR-seq lymphoblastoid silent region 6008 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (90397421..90397580) | | |
| ID: 130056272 | ATAC-STARR-seq lymphoblastoid active region 8880 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (90397241..90397290) | | |
| ID: 130056271 | ATAC-STARR-seq lymphoblastoid active region 8879 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (90384227..90384376) | | |
| ID: 129390659 | MPRA-validated peak2228 silencer [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (90419211..90419411) | | |
| ID: 127828238 | H3K27ac hESC enhancer GRCh37_chr14:90849673-90850199 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (90383329..90383855) | | |
| ID: 127828237 | H3K27ac hESC enhancer GRCh37_chr14:90849146-90849672 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (90382802..90383328) | | |
| ID: 127828236 | H3K27ac hESC enhancer GRCh37_chr14:90848618-90849145 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (90382274..90382801) | | |
| ID: 126862021 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr14:90870785-90871984 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (90404441..90405640) | | |
| ID: 123466210 | long intergenic non-protein coding RNA 2960 [Homo sapiens (human)] | | | |
| ID: 112272566 | Sharpr-MPRA regulatory region 5900 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (90396721..90397140) | | |
| ID: 157206 | ribosomal protein L21 pseudogene 11 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (90366635..90367222, complement) | RPL21_50_1399 | |
| ID: 801 | calmodulin 1 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (90396502..90408268) | CALML2, CAM2, CAM3, CAMB, CAMC, CAMI, CAMIII, CPVT4, DD132, LQT14, PHKD, PHKD1, caM | 114180 |