Tag | Content |
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EnhancerAtlas ID | HS007-06468 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr16:67250370-67251970 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF4 | MA0039.3 | chr16:67251600-67251611 | CCACACCCTCT | + | 6.02 | Six3 | MA0631.1 | chr16:67251923-67251940 | AGAGGTGATATCCTCTC | - | 6.16 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr16 | 67250768 | 67251468 | chr16 | 67250756 | 67251901 |
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| Number: 1 | ID | Chromosome | Start | End |
GH16I067216 | chr16 | 67250541 | 67251751 |
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Enhancer Sequence | ATGGCCAGCA GCCACTCCCC TTGATGCCAT CTCCACTGGG GTTCTGCAAC TCTGCCCCCC 60 TGGCTTTCCT CCTACCTTCT AGCCTGCTCT TCTTCAGGCT CTTTTGGGGT CAACAAAGAA 120 CAGAGATCCA GTCCACAGAT GAGTGGGTTC CCCATGGTTT GTTCCACCCA AGAACACACA 180 CACGTGTGCA CGTGCACATA TGCACACGAT CTTTGTGCCC CTCCGAGTGT ACCCTGGCCA 240 ACTGCATTTT GCCCCATGGG GCCATCATTC CAACCACTGT CTTTCCGATC CACATGATGT 300 TCCTGAACGC CAGACCCCGG GAGCCAAGTG CCTGACTGGC CTCTCTCCAG AGGGCACGAT 360 GCAGCATACC CAAATCTGAA CTCATCATCT CATCCTCCAA CTCTGCTCCT TCTAAACTCT 420 CCCCACCCTC TATTGAGTCA CCCAAGTGGG AAATTTGGGA GTGATTCTAG AATCCTCCCT 480 CACTCCCCAC ATCCACAATG ACCCAAGCCC CTTCCACTTT TGTTTCCCTG ATACGGTGCA 540 ATCTGTCCCT CTGCTCCAAC CTCACTGCTT CTGCCCTAGT TGAAGTCCCC ATACTGTATG 600 CCAGCAGCCC GAGAGCTGCT TCCTCTAAGC TCAGACCACG CCAGCTTCCT CCTTATCAGG 660 TCCTGGCCTC CAGTTCCTCT GGCTCCAATC CATCCTGGGT TTTGTCACCA TGTGACCCTT 720 CCAAAAGGCG ATTCTGCCTG TGCTCTCCAG ACCCTCTGCC AGTTCCGCAC GCCTCCAGGA 780 CACAGGCTAA GCTTCCTAAG CCTGCATTCA AGCCCTTCTA GGACCCAGGC CTGCTGCTTC 840 AGCCAAGCTC TTCCCAAGCC CGTTCCCCTT CCTCCTAGTC CTGGCTCTGG GGCTGCCACT 900 TCTGACCATT GTCCTGTACC GCACGCCTCT GCTCAGCTGC TTTTTCTGTT CTGGGGGGGT 960 CCCACCCCTC ACTGGCTCCT ATTGGTCTAT TTGGCAAATG TTTATTCCTC TCTCGAGTCT 1020 CAGGCCAAGC ACCTCCTTCT CCATGGAGTC TTTTCTGATC TTTTCTCTGC ACCCATGATG 1080 TGCCTCACAC AGACTTCAAA TGCAGCACCC CAGCCTCTTT TTACTCATCT GTACTCACTA 1140 CACACTCCCC AGCCCTGTGC CTTCCTCAGT TTTGCCTCGC TGGTGCCCAG CACACTGCCC 1200 GGCACAGCAG AAACATTTGA GTAAGGCTGC CCACACCCTC TCTATGTGTC TCTGGTAATT 1260 TTCCATCTTC CTCCTGTCCT GTGACTGCTC CAACCCTCTC TGCTGAAGCC CTGGCCTCTA 1320 TGTCTCTTTT TACTCTCCTG AGACAACCTG GTCTCCAAAT CCACTGAGTG AAGGGGCCGC 1380 TGAGGAAGGA GATGCCTCTG AGGAACTTCT CTGCAAATAG CTCCATGTTT CCACCCCCAC 1440 CTCTCTGCTT CCTCAGGAAG AGGTGACATC CTTTTTTTCA CCAAACTGAT GCTGAAAAAA 1500 CAAAAAAGAA AAACACACAC ATACACACAC AAAAAAACAA AAAAAAAAAA GGGAGAGGTG 1560 ATATCCTCTC CATCCTATCC CAGATCAAGC TTGGTATGTG 1600
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