Tag | Content |
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EnhancerAtlas ID | HS040-19177 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr2:18074110-18074910 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFE2L1 | MA0089.2 | chr2:18074431-18074446 | TCTGCTGAGTCATGC | - | 7.23 | Nfe2l2 | MA0150.2 | chr2:18074433-18074448 | TGCTGAGTCATGCAG | - | 7.41 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 18074112 | 18074343 | chr2 | 18074367 | 18074908 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I017892 | chr2 | 18073975 | 18074891 |
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Enhancer Sequence | GGTGCAATGG ACTCCATGAG GATCCTTAGC TTTGGTGGTT TAATGCTCTA TTTTTTTACT 60 GGTTGGCCGC CTGCCAGGAG GCGGCACTTT CAGCTGTGCT AGTATGGGGA GGAACCAGCA 120 GTGGGTGGGG CCCTAGAACT CTCAAGATTA TATGCCCTTT GTCTTCCATT ACCAAGGTGG 180 ATAGGAAAGG ACCATCAGGT GGGGGTAGGG CCAGGCACAT GTGTCTGAGC TCAGACTCTC 240 CTTGGGTGGG TCTTGCTGTG GCTGCTGTGG GGGATGGAGG TGAGATTCCC AGGTCACTGG 300 AGTTGTGTAC CTATGGCTGC CTCTGCTGAG TCATGCAGGT TTTCAGTTAA GTGGGGGAAA 360 GCTGGCAGTC ACTGGCCTCA CCCAGTTCCC ATGCAAACTG AAGGGCCGGT CCCACTCCCA 420 CCCTGTCCCC TCCTACAGCC TGGAGTCTGT TTCCAGGTGG AGAGTGAGAG GGTCTTGAAA 480 ACTTGCCCGA GGCCATCTGC CTCCCAGCTG AGAAAGAAAG GGCTTTAATT CTTCCTGGCC 540 TGTGAAGTCT GCATGCCGGA TTAGGATTCG CAACCTCTCC TGAGTTCTGG CCAGGGGGCT 600 TCTCGCCCCG TTCAAATTGT TACAGAGTTT GCCTAGAGAA TTCCTTCTCC TTGTTGAATT 660 TTACCCCCTG CATCTCTGGG CACCCTCATG ATGGATCCCC GTGGTGCCAG GCAGGAATGG 720 ACTGCTTGGG GACCCAGTGA GCTCCCAGGG CTTTTCTGCT GCTTCCTCTG TATTTCGCTC 780 GGCTCTCTAA CTTGACTCAG 800
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