ID: 127894965 | H3K4me1 hESC enhancer GRCh37_chr21:46075541-46076041 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (44655624..44656124) | | |
ID: 127894964 | H3K4me1 hESC enhancer GRCh37_chr21:46075040-46075540 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (44655123..44655623) | | |
ID: 127894963 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr21:46067006-46067870 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (44647089..44647953) | | |
ID: 386684 | keratin associated protein 12-4 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (44654213..44654659, complement) | KRTAP12.4 | |
ID: 386683 | keratin associated protein 12-3 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (44657932..44658341) | KRTAP12.3 | |
ID: 386678 | keratin associated protein 10-11 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (44646414..44647650) | KAP10.11, KAP10.9, KAP18-9, KAP18.11, KRTAP10-9, KRTAP10.9, KRTAP18-11, KRTAP18-9, KRTAP18.11, KRTAP18.9 | |
ID: 353333 | keratin associated protein 10-10 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (44637356..44638455) | KAP10.10, KAP18.10, KRTAP18-10, KRTAP18.10 | |
ID: 353323 | keratin associated protein 12-2 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (44666189..44666927, complement) | KAP12.2, KRTAP12.2 | |
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 |