Tag | Content |
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EnhancerAtlas ID | HS012-15659 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr19:45548730-45549980 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ELF5 | MA0136.2 | chr19:45548828-45548839 | ACCAGGAAGTA | + | 6.02 | PLAG1 | MA0163.1 | chr19:45549756-45549770 | CCCCTGTGGGCCCC | - | 6.86 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_05663 | chr19:45546684-45553894 | Brain_Cingulate_Gyrus | SE_06624 | chr19:45546489-45556859 | Brain_Hippocampus_Middle |
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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 |
GH19I045044 | chr19 | 45547947 | 45551861 |
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Enhancer Sequence | TACCACTGCA CTCCAGCCTG AGTGGGAGAA TAAGACCCTG TCTTTAAAAA AAAAGTTTCG 60 GGATGTTTTC CCGTAACATT TCCACTCCTC CCCTGCTGAC CAGGAAGTAG TCTTATGAAC 120 AGCCGTGAGG AAGGCTAAGA GGTGTAGACT TTATTTTGGG TCGCCCTGAC CAGATATATT 180 TGGAGTTCTG TTACTGTTGT AGCAAAGGGA ATAGATGTTG GTTGCCAATT AATGGTTTGC 240 CACTAACAGT GGAGACAAGA GCATGTCCTT CGATGTTGTT GGAGTGTTGG ACACATGGAC 300 CACTGAGAGC AGCCTGGCCA GCGTCGCTAT CGCTCAGTAA ATATTAGCTC TTGTTATTGA 360 CATTACTGTT GCTGATAGAA CTGGAGTTTG GATCCAGGTG GAGGGATGGT GCAGAGGAAG 420 GAAGGCTGGA GCTGAGACTC CAGGCCCCCT CCCTGTTAGC AGGGAAGCTT GCTGCATTGT 480 ATTCCCCCTC AGGACAGTGG TGACGACCAA CCCCTCTCAC TGGATAATGG GGAAGAGCTC 540 AAAGAACCAA TGTCTATGGG TGCTTTGTGG TGCAGGCCTG TACAAGCGGC CTTTGTCCCT 600 GTATGTGAAC GTGACCTGCA TTCCGATCTG GGCTGCCAAG CTGTGGAGTA TGGCTGGGCC 660 GTGGCTGATG GCTGCTTTGA GGAGGGGACT CTCATCTCAG CCTTGGGCCG AGAGCAGAGG 720 CTGTGGAGCG AGTGTCAGTG AAGCTGCGGT AGATTGTGGC AGGCTGAATG AGTATGTCCA 780 GATGCAGTTG GTTTCTGTCT TCCTGATTTG TCGTTGGTGC CTGCTTTCTC TCCCTGTCTT 840 CAGTCCCAAG CAGACTCCGG TTCTGTCATT GCTTCTGTCC TTGTCAACTT TCCTTTTTAA 900 TCAGTGGTTT GGATAAAGAA ACAGAATCCT CTGTTGATAC GGAAATAAGA AGTAAACAGG 960 TCGCAGCTCA GGCGTCGCCT CCTCCAGGAA GCTCCAGACT GACCCCCAAG TCTGGGTCAG 1020 GTGTTCCCCC TGTGGGCCCC CATCTCAGCG CTGTCCACTC TAGGTTGTCC TTGTATGGGG 1080 ACAAGTCTGT GTCCCACACT GGACTGTGAG CCCATGAGGG CAGGGCCAGG GCTATCTCAG 1140 TTACTGCCAT ACCCTAGCAC AAGGTCTGCT TAACAGTTGA ATGAATGAAT GAATGAATGA 1200 GTAACTTCAT GAACTCCTCT GACACAATCT GATCCTAGAG ACAGGATAAT 1250
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