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Links from Gene

Items: 14

    • Showing Current items.

    Name/Gene IDDescriptionLocationAliasesMIM
    ID: 127894962
    H3K4me1 hESC enhancer GRCh37_chr21:46045935-46046630 [Homo sapiens (human)]Chromosome 21, NC_000021.9 (44626018..44626713)
    ID: 127894961
    H3K4me1 hESC enhancer GRCh37_chr21:46036915-46037661 [Homo sapiens (human)]Chromosome 21, NC_000021.9 (44616998..44617744)
    ID: 127894960
    H3K4me1 hESC enhancer GRCh37_chr21:46032635-46033283 [Homo sapiens (human)]Chromosome 21, NC_000021.9 (44612718..44613366)
    ID: 127894959
    H3K4me1 hESC enhancer GRCh37_chr21:46031985-46032634 [Homo sapiens (human)]Chromosome 21, NC_000021.9 (44612068..44612717)
    ID: 127894958
    H3K4me1 hESC enhancer GRCh37_chr21:46022863-46023717 [Homo sapiens (human)]Chromosome 21, NC_000021.9 (44602946..44603800)
    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: 386681
    keratin associated protein 10-8 [Homo sapiens (human)]Chromosome 21, NC_000021.9 (44612079..44612954)KAP10.8, KRTAP18-8, KRTAP18.8
    ID: 386676
    keratin associated protein 10-9 [Homo sapiens (human)]Chromosome 21, NC_000021.9 (44627093..44628378)KAP10.9, KAP18.9, KRTAP18-9
    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: 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: 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-EAR612920
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