Tag | Content |
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EnhancerAtlas ID | HS012-15849 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr2:16233740-16235330 |
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) |
PAX6 | MA0069.1 | chr2:16235138-16235152 | TTCACGCTTGAGCT | + | 6.55 | POU2F2 | MA0507.1 | chr2:16234612-16234625 | TGCATTTGCATGT | + | 6.37 |
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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 | CAGATATCTC TGGGCTCTTG GGAGAAACAG AGCCCTGTGT TTCCAGGTAG GTAGGCTTCC 60 TGGAGGAGTT GACACTTTAA CAGAGATTTA AAGGATTGGC ACAAGCTATA TGGAAGAGGA 120 GGTGTGGGGT TGCATTTGAG GCCTGGATGG AACAAATGGT CAGAATTGGC TCTGGGTAGA 180 ACAAATGGTG GGGCAGAGGG TGAGGCTGGG GAGCAGGAGG AAGCCAGCCC CGCAGGAGGC 240 AGCATGAGCT TCCTGGCCAG GGTCCTGAGG AAAGGCATCA AGGGACCTCC GGGGAGCATG 300 GCAGGGCTTT CCTGTTAGAG CCTCCTGATG ATGATGGACT GTGGTGTAGA AGGATGCATG 360 CCAGCCGTGG GCTGAGGCTG TGATCCACAG AGACGAGAAC CCACCCAGGG CAGCAGCTTT 420 GGGGCTCATG GCAGAGCCTC CGCCCTCGGC TCCAGTGGGA TAATAGGGCG ACATGACAAG 480 CTCTTCGTGC TCCCTGGAGG CTTGGTGCTC CCCCTGGCTG GATGTCAGAA CAAATTAAGG 540 GCACTTGTCT CACAAGCCCC ACCTGGCCGG CAGCGTCGTG GGGCCGGCTG GCAGGGGAAA 600 TGTGTCACCA GCAGCATCTT GGACCTTGGC CATTGGCCTC AGAGCAAGAA AAGCTCTCTC 660 TGCCCTGCCT GTTTAGTGAA CAATGTACAG GAGTACAAGA GACTCTATGG CAACCAAAGA 720 CCTGTGTCAG GGTCATGGTT CGAGGTTTTC TGTGCTCACT AATGTGGAAA ACAGAAGCCT 780 CATGCTACAT CAGCATCGCG GCTGGTTTAC ATAAGCAGTC GGAGGCTGCA CAGAGCCAGA 840 GCTGGAGCTG GGGCCGGGGC AGCTCCACAT CTTGCATTTG CATGTTGCTA AGTGTGCATG 900 TGTACATGAT CTCCTTTGAC TTCACAATAC CCTGTAACTC TGGGATTCCT TGTTATCCCC 960 ATTTTACAGA CAAGGAAACC CTGTAGGTTC CAGGGAGGGG CAAGGACTTA CCCAAAGTCT 1020 GATTCTAACT TCAGTGCTCT CTTGAATTGA CTAGATGTGG AGGCGTCTCA GAGCTTGGTG 1080 TAACGTGAGC TGGTGGGCAG AGTCCCCTTC CCCACCAGTG TCTCCCTGAG TCCTGATGCC 1140 AGGAGGGCAG GGCCCCCTAA GGTAGGGCAC CTTGAATGCA TCCTGGGCTG ATTCTGGGGT 1200 CTGAGGACCA AATGGCTGGG AATGAAACAG GGACAATGAG TTGGATGTTT TCATCCAGTG 1260 CTTGGAAGCC GTCCTGGAGT TACCACTAAC AGTGCTGAAG AGTGGAGAGC CTCTGGGTTC 1320 TGGAGAAACA CCTGGGCCCA TGCTGTCCCT TCTTCCTGAA AGCTCCTCTT CTCCTGTCCC 1380 TGCATGAGGC TTCGCCCCTT CACGCTTGAG CTAGCATATC CTGTTATCTG CAAAGTGTCT 1440 TGAATCTCTC ATCTGGGCTG GGTGCCTCCA CTCTGTCTGC TCACTGCTCT TGGGACACCC 1500 CTCCCACAGC GCTTATGCCA CTCTCAGGTC ACGGCTTCAT TTGTGCTTTT CATTGCACGA 1560 AGACAGAGAC CTCCCATGGG CCCTCAGATG 1590
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