Tag | Content |
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EnhancerAtlas ID | HS095-14073 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr18:60000930-60001890 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr18:60001317-60001332 | TGAACTCTTGACCTC | - | 7.64 | RARA | MA0729.1 | chr18:60001314-60001332 | TCTTGAACTCTTGACCTC | - | 6.45 | TFAP2C | MA0524.2 | chr18:60001736-60001748 | AGCCCCAGGGCA | + | 6.11 | Zfx | MA0146.2 | chr18:60001342-60001356 | CCCGCCTCGGCCTC | + | 6.01 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH18I062333 | chr18 | 60000941 | 60002330 |
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Enhancer Sequence | TTGTATAGTC AACTCTGTGA TGGGGTAGGG AGTAGAGAAA GGGACCTCCC AGAATGGTGG 60 GACAGAAAGC TTTTTGGTAT TTGGGGACAC CCATGCAAAT GCGTGCCCAG TCTGCATTTG 120 TGGGGGTCTG TCTTGTCTGC TCAAGTATGT ACTCACTGAG GGCTTTCTAG AACTTTTTTT 180 TTTTTGAGAA GGAGTCTCAC TCTGTCGCCT AGGCTGGAAT GCGGTGGTGC CATCTTGGCT 240 CACTGCAACC TCCGCCTCCC CCATTCAAGC AATTCTCCCT GCCTCAGCCT CCCGAGTAGC 300 TGGGATTACA GGTGCTCGTC ACCATGCCAG GCTAATTTTT GTATTTTTAG TAGAGACGGG 360 TTTTCGACAT GTTGGCCAGG CTGGTCTTGA ACTCTTGACC TCAAGTGATC TGCCCGCCTC 420 GGCCTCCCAA AGTGCTGGGA TTGCAGGCAT GAGCCACCGC GCCTGGCCTC TAGAACTATT 480 CTTAAGCAGA AATGGCAATG CTGTGTCTTT AAGGCTAATC CAGATAAAAG GCACTCCAGG 540 CACTCTTGGC ACAGGGTCCA TGTGCCAGTT GATCCCTGAC TCAGGAGGAA AAGAAGTGTA 600 TGTCTTGAAT CACCACCACT TCCTGAAGCC AAGGCAGCAC TGGCTCGTCT ATGCCCCACA 660 CCCCAGAGTT AGACTATACC GTACCACTGT GCTGTAGCCC TGGGTGTACC GCCTCAGAGG 720 GTCGCATCTC TCCACGCGTG TTCATCCCAC TCCCACCACC TGCCAGGCTC TGTGTAGGGT 780 GGGAGGAGGG AGAAGGATGG CCTTGGAGCC CCAGGGCAGC AGACAGTGAT AGGTTAAACC 840 TTTGCCCTCA TAAGCTTTCG GAAGTAGGTA GTTATATTTT TAAAGGTCCT TTATGTCTTA 900 GTCTTACTAC AATTATAGCT AATCTGGGGA CTCTTCCCTT GATGAGAATA ACCTGGGCTC 960
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