ID: 127894949 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr21:46000216-46000805 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (44580339..44580928) | | |
ID: 127894948 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr21:45999625-46000215 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (44579748..44580338) | | |
ID: 127894947 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr21:45994339-45994857 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (44574462..44574980) | | |
ID: 127894946 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr21:45993821-45994338 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (44573944..44574461) | | |
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: 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: 386680 | keratin associated protein 10-5 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (44579455..44580604, complement) | KAP10.5, KAP18-5, KAP18.5, KRTAP10.5, KRTAP18-5, KRTAP18.1, KRTAP18.5 | |
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: 386672 | keratin associated protein 10-4 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (44573729..44575371) | KAP10.4, KAP18-4, KRTAP10.4, KRTAP18-4, KRTAP18.4 | |
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 |