| ID: 127894957 | H3K4me1 hESC enhancer GRCh37_chr21:46022006-46022862 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (44602089..44602945) | | |
| ID: 127894956 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr21:46021146-46021905 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (44601231..44601990) | | |
| ID: 127894955 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr21:46020385-46021145 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (44600481..44601230) | | |
| ID: 127894954 | H3K27ac hESC enhancer GRCh37_chr21:46018864-46019624 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (44598964..44599720) | | |
| ID: 127894953 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr21:46012727-46013473 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (44592846..44593592) | | |
| ID: 127894952 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr21:46011981-46012726 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (44592100..44592845) | | |
| ID: 127894951 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr21:46011233-46011980 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (44591352..44592099) | | |
| ID: 127894950 | H3K4me1 hESC enhancer GRCh37_chr21:46009439-46010260 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (44589559..44590379) | | |
| 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: 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: 386675 | keratin associated protein 10-7 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (44600597..44602174) | KAP10.7, KAP18.7, KRTAP18-7 | |
| ID: 386674 | keratin associated protein 10-6 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (44591268..44592505, complement) | KAP10.6, KAP18.6, KRTAP18-6, KRTAP18.6 | |
| 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 |