| ID: 130059321 | ATAC-STARR-seq lymphoblastoid active region 11047 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (69824301..69824370) | | |
| ID: 130059320 | ATAC-STARR-seq lymphoblastoid active region 11046 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (69824191..69824290) | | |
| ID: 130059319 | ATAC-STARR-seq lymphoblastoid active region 11045 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (69773284..69773483) | | |
| ID: 130059318 | ATAC-STARR-seq lymphoblastoid silent region 7667 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (69762759..69762808) | | |
| ID: 129663866 | ReSE screen-validated silencer GRCh37_chr16:69967565-69967755 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (69933662..69933852) | | |
| ID: 129663865 | ReSE screen-validated silencer GRCh37_chr16:69964206-69964363 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (69930303..69930460) | | |
| ID: 128966615 | C-type lectin domain family 18 member C-like [Homo sapiens (human)] | | | |
| ID: 127884407 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:69986397-69987010 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (69952494..69953107) | | |
| ID: 127884406 | H3K4me1 hESC enhancer GRCh37_chr16:69984558-69985170 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (69950655..69951267) | | |
| ID: 127884405 | H3K4me1 hESC enhancer GRCh37_chr16:69983944-69984557 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (69950041..69950654) | | |
| ID: 127884404 | NANOG-H3K27ac hESC enhancer GRCh37_chr16:69924551-69925074 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (69890648..69891171) | | |
| ID: 127884403 | H3K27ac hESC enhancer GRCh37_chr16:69796040-69796618 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (69762137..69762738) | | |
| ID: 127884402 | H3K27ac hESC enhancer GRCh37_chr16:69788499-69789121 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (69754596..69755218) | | |
| ID: 127884401 | H3K27ac hESC enhancer GRCh37_chr16:69787875-69788498 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (69753972..69754595) | | |
| ID: 126862385 | MED14-independent group 3 enhancer GRCh37_chr16:69950984-69952183 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (69917081..69918280) | | |
| ID: 119139903 | NQO1 divergent transcript [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (69726727..69743918) | FASRL | |
| ID: 644035 | non-POU domain containing, octamer-binding pseudogene 1 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (69755416..69758070, complement) | | |
| ID: 406932 | microRNA 140 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (69933081..69933180) | MIRN140, SEDN, miRNA140, mir-140 | 611894 |
| ID: 348174 | C-type lectin domain family 18 member A [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (69943519..69966623) | MRCL, MRCL1, MRLP2 | 616571 |
| ID: 28987 | NIN1 (RPN12) binding protein 1 homolog [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (69741871..69754926, complement) | ART-4, MST158, MSTP158P, PSMD8BP1, NOB1 | 613586 |