| Tag | Content |
|---|
EnhancerAtlas ID | HS104-12745 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr12:2953880-2956050 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Ar | MA0007.3 | chr12:2954776-2954793 | GGGCACAGGGTGTTCTG | + | 6.15 | | GLI2 | MA0734.2 | chr12:2954530-2954545 | CAACGTGGGTGGCCC | - | 6.79 | | NFIA | MA0670.1 | chr12:2953903-2953913 | ACTTGGCACC | - | 6.02 | | RREB1 | MA0073.1 | chr12:2954913-2954933 | CCCCACCCCACCCCACCAAA | + | 6.45 | | ZNF263 | MA0528.1 | chr12:2955800-2955821 | CCCTCCTTTCCACCCTCATTC | - | 6.42 | | ZNF263 | MA0528.1 | chr12:2954677-2954698 | GGGGGAGGTGGAGGGAGGGGA | + | 7.19 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I002844 | chr12 | 2953885 | 2956121 |
|
Enhancer Sequence | CCTTGCCTAA GCTGTGGGCC TGCACTTGGC ACCCTTGGAC ACGACCTCCC CTTCCTAGTG 60
ATACTCAGAC TAAAGAAGTC ACTGACTATT GTTTGGGAAC CATGTCATGA TACCTAGTGT 120
CAACGTTCCA TAAACACCCA GTAAACATAA GTGTGGTCTA AGGGAAGCCA CACATCGAAA 180
TTCCTGTCTT GGAATTTGGA CAATGGCAAG ATGCAGCCAC ATTCTTTACA AGCGTGGAGG 240
CGTTCGTGAG GCTCTGCCCT GGGACTGGCA GGGAATGAAC TGGCTTGGGA CTAACATAAG 300
TGGAGCAGCT ATGTGAAGAG CCACGGGAAC CGCTACCTGT GATGGCAGGT GGGCAGCAGC 360
CACTATTGAC ACTGTGTAAT GAAAAGAGCA AATGTGTGCG GCTCGGTGGC AGCACAACTA 420
AGGACAGGGC TCAGTGATGG AAAAGAGGCA TGAAGACAAG GGGCTCCCAG CAAGTGAGGC 480
AGCGATGAGT TGGAATGAAG GCTGGAGGGT CGCAGGGAAG CTGGAAAGTG AGTTGGGTGG 540
GGACTGTCTG CAGAGGGGAT CTTGGCTCGA GTTTGTCATC TCAAGGAGCA GCTATGGGGC 600
TTTTTGAGGC ATGGTAATTA GATGAGACAA CCCTGGCAGG GCATGACTGG CAACGTGGGT 660
GGCCCTGTAT GGTCCCCCAG GGGTTCCCAG TCCCCACAGC TTCCCGACTC CCTGGCCCCA 720
GCCATTCCTC AAGCTCCCAG CAGCTCAGGA ACTTGCGTCA GCAGCTCAGG TCATGACACC 780
AAGATCAGGC TTGGAAAGGG GGAGGTGGAG GGAGGGGAGT TTTTGGCCCG GAAATGGCTG 840
GGAAGACTTC CTTTGCTGGG ATTAACTGTT GTCCGTGAAG CTGGTGGCAT TCAGCAGGGC 900
ACAGGGTGTT CTGGGGAGTG AAGTATGTGG GGGAAAGGGG TGTCCATACC TTCACCCCTG 960
CCTCCCTCTC AGAGCTGCAC TCCAGCTGTG GTGAAAGAGT GGATCTTTAG GCAGATACAG 1020
ATACAGAGAT TCCCCCCACC CCACCCCACC AAAGGCTTTC AGGACCTCTA GGTTCATTCG 1080
TGTGTGGGGA TGGAGTAAGG AGGTTGCTCA TGCTTGCCAG CCAAGTGTAT GTAGGCTGAG 1140
CTGGGGTGAT TTTCTTTTTC TTTTTTTTGT TGAGTTAGGG TCTCACTGTA TTCCCCAGGC 1200
TGGTCTGAAA CTCCTGGGCT CAAGCGATCC TCCTGCCTCA GCCTCCCAAG TAGCTGGGAC 1260
TACAGGTGCA CACCACTGCA CCTGCCTGGC TGGGGGTTGC CTCGTTAGGG TCCCCAGGCC 1320
CGGAAGGTCG CGTGCTTGCT ATTGCTGCCC CGCAGACCCC CATGGCCTGC TGGAGCTAGG 1380
GGGCGCCAGA AGCCTTACTT CTGTGTCTCT GGCCGATGAA CAAGAGAGCC TGGATACTGC 1440
TGCAGAGCAG AGGCTGTTCC GGAGAGCAGG GCTGGAAGGT GGTGGGGCGG GGTGAAGTCC 1500
TGACTAGAGG CTGGGAGCTT CTGGGTGGGC AGGGTCTGCC AGGGCAGGAG CCTGTGTGAG 1560
TGCAGCTTCC TTTCTGCCCG CCCCTAGCTT AAGGCCAGAG AGTAGGCAGC TTGTTTTCAA 1620
GAATCCCAAT GGCTTTCTTC CTCCCACTCC CTAAATCTTC TTGCCCACCC TCTAACCATG 1680
CCCAGGGCCT CTCGCTGTGA GGTGGCAAGT AGCCCGAGAA GCAGATGGTA GCCCAGGCCT 1740
TGCAGTCCCC GCTCCAGCAC ACCCCTCCCG TCCTCTCGCC AGGAGGCTGC CTGGCTTTGT 1800
GGTCCGGAGC AAGTCACTTC TCGACGGGCT TCACTTTGCC CATCTGAAGT CTGAGGTTGT 1860
TAGGCGTGTT TTCTAATGGC CTGCCCAGCT CTGACATTTT TGGATCCTAT GTAAAGGGAA 1920
CCCTCCTTTC CACCCTCATT CCCAGTCCAG AGTGAGGAGA TTGGGTAAAT TCCCAGAGCC 1980
CTGGCACTCC CGTGGAGCAC TCAGGAAACG CTCCTTCACC CCTCAATTCT GCTCTCACAC 2040
ACCCCGTCAC ACATAGACTC ACATACACCA AGCAGAGAGG AGCAAAGAGA AGGACCATGT 2100
AAGACAATCA CGGACATGGC GTTAGAAGGA AACTGAGAAA CGCTCTACAA GAGTTCGATG 2160
TATTACATTA 2170
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