Tag | Content |
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EnhancerAtlas ID | HS012-15850 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr2:16236650-16237800 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr2:16236791-16236806 | TGAACTCTTGACCTC | - | 7.64 | RARA | MA0729.1 | chr2:16236788-16236806 | TCTTGAACTCTTGACCTC | - | 6.45 |
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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 |
GH02I016093 | chr2 | 16233591 | 16238433 |
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Enhancer Sequence | CAACCTGTGC TTCCCAGGTT CAAGTGATTC TCCTGCCTTA GCCTCTTGAG TAGCTGGGAT 60 TACAGGTACA CACCACTGTG CCTGGCTCAT TTTTGTATTT TTAGTAGAAA CGGGGTTTCA 120 CCATGTTGGC CACGCTGGTC TTGAACTCTT GACCTCATGG TCTGCCTGCC TTGGCCTCCC 180 AAAGTGCTGG GATTACAGGT GTGAGCCACC ACGCCTGGCT GGAGTCCTTT ATTGTTGCAC 240 TAAAGTCAAA AAAGAATTCT TGGCCAGACG ATGTATAAGC ATCTTACATT GTATGGTGTT 300 TCTCAGGTTC CAAAAATCTT AGCAGAACTC GTTTCATTCA GGGCTTACAG TTTCCTGGTG 360 GGGATCATCA ACCCCATCTT ACAGTGATGG AAACAAGTCT AGAAGGGAAT TAACAAAGAT 420 TTCTTCAGTG TCAGCAACTG ATGGAGCTGG AAGTAGATCT AAATAGCCTG TTTCAAACCC 480 AGAATTCTCT CCTGTACTCC AGGTAACGCC ACTGGTTGTG GGCAAAATCC ACCTGTGAGC 540 CACAGTCTAG TCTTACGAAA TTGTAAAACG GATGCAGGGG GTGAAATTTC CTTTTTAATG 600 TTTTAACTTT AGATTGGCCT TCTGCCTCTG ACTCTAGAAT GGTTTGTACT GAGTAAATAT 660 TAACCCAGGG CTCCATGGCC AGTGTTTTAT GAGCTGGTGG AATGCCCTGC AGCAGGGGCT 720 GGGGAGAGGG GAATTGGCTG GCCCCACATT TGAAGATGGC ACCTGATGCT TGGGTCGGCA 780 AATGTCTGAA AGGCTTTGCA GCTTGCTGGG CAGCCCAGGT GGGAACTTAC CTCTTGGTGA 840 AAGCATCAGG AATCTCCCAA TCCCTCAGGT AACCCCGATC CCTCAGAATA GATCAGATGA 900 TGGCCGGGAC TTGTATTGGT TCATTTTCAC ACTGCTGATA GAGACATACC GGAGACTGGG 960 TAATTTATAA AGAAAAAGAT GTTTAATGAA CTCACAGTTC CACGTGGCTG GGGAGGCCTC 1020 ACAATCATGA TGGAAGGCGA TAGGCACGTC TTACATGGCA GCAGCAAGAG AGAATGAGAG 1080 AACCAAGTGA AAGGGATTTC CTCTTAGAAA ACCATCAGAT CTTGTGAGAC TTATTCAGTA 1140 CCATGAGAAC 1150
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