| ID: 130066830 | ATAC-STARR-seq lymphoblastoid silent region 13385 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (44510724..44510773) | | |
| ID: 127894945 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr21:45970519-45971066 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (44550636..44551183) | | |
| ID: 127894944 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr21:45969969-45970518 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (44550086..44550635) | | |
| ID: 127894943 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr21:45958816-45959480 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (44538933..44539597) | | |
| ID: 127894942 | H3K4me1 hESC enhancer GRCh37_chr21:45957963-45958462 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (44538080..44538579) | | |
| ID: 127894941 | H3K4me1 hESC enhancer GRCh37_chr21:45939631-45940180 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (44519748..44520297) | | |
| ID: 126653398 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr21:45928270-45929469 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (44508387..44509586) | | |
| ID: 124905038 | uncharacterized LOC124905038 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (44527509..44533182) | | |
| ID: 112694751 | Sharpr-MPRA regulatory region 850 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (44549026..44549320) | | |
| ID: 386682 | keratin associated protein 10-3 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (44557790..44558795, complement) | KAP10.3, KAP18-3, KAP18.3, KRTAP10.3, KRTAP18-3, KRTAP18.3 | |
| ID: 386679 | keratin associated protein 10-2 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (44550357..44551505, complement) | KAP10.2, KAP18-2, KAP18.2, KRTAP10.2, KRTAP18-2, KRTAP18.2 | |
| ID: 386677 | keratin associated protein 10-1 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (44538981..44540195, complement) | KAP10.1, KAP18-1, KAP18.1, KRTAP10.1, KRTAP18-1, KRTAP18.1 | |
| ID: 114043 | TSPEAR antisense RNA 2 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (44517215..44518977) | C21orf90 | |
| ID: 54084 | thrombospondin type laminin G domain and EAR repeats [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (44497893..44711572, complement) | C21orf29, DFNB98, ECTD14, STHAG10, TSP-EAR | 612920 |
| ID: 54082 | TSPEAR antisense RNA 1 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (44506044..44516575) | C21orf31, C21orf90, TSPEAR-AS2 | |