Tag | Content |
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EnhancerAtlas ID | HS050-17558 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr12:122952410-122953140 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Lhx3 | MA0135.1 | chr12:122952913-122952926 | TAATTAATTAATT | + | 6.78 | Lhx3 | MA0135.1 | chr12:122952914-122952927 | AATTAATTAATTT | - | 6.92 | POU6F1 | MA0628.1 | chr12:122952915-122952925 | ATTAATTAAT | + | 6.02 | POU6F1 | MA0628.1 | chr12:122952915-122952925 | ATTAATTAAT | - | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_27577 | chr12:122952079-122953267 | Esophagus |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr12 | 122952702 | 122952803 | chr12 | 122952584 | 122952853 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I122466 | chr12 | 122950812 | 122953434 |
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Enhancer Sequence | AAAAAAAAAA AAAAAATTTA CCTAGAGGGA AAAAAAGTAA AAAAACCCCA ATTCAAGACA 60 GAAAAAAGCA AAATGATTCC AGCCGAGAAC TTGAAGAATA AAATCAACCA GGAGGACGCT 120 TCATGTTAGT AGAAAGTGGA CGGCATTTTC ACCATGTAAG GAAATGTGAC CTTTTGAAAA 180 AAGAACGAGG TCGTTTTCTA TTTTAATAAG GGCAGTTCCT TCTTTCCACT TACCTGCTTC 240 TAGGAGACAA CAACAAAGAG CTGGCCTTGT TTTAGCAACC TGCACTGCAG TTTACATTCC 300 CTTTAACCCA AGACAAAGAT TAAAGAGATA TCCCCACCCC TGCTCCAAGT CAATCTTGAA 360 GGACAAACGT CTGGTTCTTA CCTCATCTAC CCACACCTGG AACCTGTCAT GGCATGGGCA 420 AGTTGAAACA GTAACTTGTT CCTCCACCCA ACAGTCTTGC AATACTCCAA AACAGCAAAC 480 AATACTTCTT TATTTTATTA CTTTAATTAA TTAATTTATT TTTTGAGACG GAGTATTGCT 540 CTTGTTGCCC AGGCTGGAAT GCAATGGTGG GATCTCGGCT CACCGCAACC TCTGCATCCC 600 GACTTCAGAT GATTCTCCTC CCTCAGCCTC TCGAGTAGCT GGGATTACAG GCATGTACCA 660 CCACGCCTGG CTAATTTTTT TTTTTTTTTT TTTAGTAGAG ATGGGGTTTC TCCATGTTGG 720 TCAGGCTGGT 730
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