Tag | Content |
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EnhancerAtlas ID | HS180-08694 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr11:58426820-58428160 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr11:58427040-58427051 | GGTGACTCATC | + | 6.32 | FOSL2 | MA0478.1 | chr11:58427039-58427050 | GGGTGACTCAT | + | 6.14 | JUNB | MA0490.1 | chr11:58427039-58427050 | GGGTGACTCAT | + | 6.32 | JUND | MA0491.1 | chr11:58427040-58427051 | GGTGACTCATC | + | 6.62 | Zfx | MA0146.2 | chr11:58427248-58427262 | GCAGCCCAGGCCTG | + | 6.2 |
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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 |
GH11I058658 | chr11 | 58426124 | 58428314 |
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Enhancer Sequence | GAGAATAGAT TAAATAGATG ATATTCAAAG CAGAAGCATC TGAACACAAG AGGAGAAAAA 60 CAATTTTCAT AAGAGCAAAG TTTAAAAGTA ATTCACTAAA AATAAGATTG TTTGAAAAAA 120 CATAACATCA GGAAAATAAA AAGAATATTT ATTCATAATA ATAGTTATTA TTCCTCATAA 180 GGAAAGCTCA CCTGAGACTT GGTGTCTAGT TTTTATTGGG GGTGACTCAT CGAGGCATGG 240 AGTCATATAT TGACCTTAGC TACTTAGTCA CCAGCCCTAT ACCCCACCCC AGAGGTCAAA 300 TTGAATACAG TGAGGCCCAA GGCCCCAGGT GAATGGAATG AAAACAGGTG TATTCCAAAG 360 GCTCACAGGT TATTTACGAG AGTTGTTTAT CACAGGCCAG TCTTTTCTTA GAAAAATGCA 420 GGATTTGAGC AGCCCAGGCC TGCTGAGTTA TGCTTGCTCC CAGGTGTGTT TAAGATGAAA 480 GTAAAATATA TAAAATGAAA AGGCAAAAGT GTAAGGCCAC TAAGGTTAAA ATCACCCAAA 540 AATGATTGAA AGAAAAAAAG AAATTGCAGC CAATTATTAA TCAGACTTGA AGTCTGTAAG 600 GCGTTTACTG AGAAATTCCT TAGAGTAAGG TTTCCTGCTG AAGCAACAAG CTGTCTTTCT 660 TCCTGAAGCA GGGCTTGGCA GAGAGCTGTG AAATACCCTG TGGTTTGCCA GGCTCTTCAT 720 CTCATGCTCT GATTATATGT ATTTTCCTGC AGGGAGTTCT ACGGGGCAGA ATCAGCTATA 780 GCTTCCCCAG CAGCATCTAT AGAGTAGGTC CCACCCACTG CACAGTGAGG CTGCTGGGGC 840 ACTTACAGCA GGAGAATCTG CAGCACTTCT GAACCAAGTC TGCAGAGGGG ATGGCTCAAC 900 TGGAGAATCA GCCATATATA AGGAGTAGCT GAGCAATTAG AGGGAACTAG ACTAAGAAGT 960 AGATTGGGAT CTTTGTCCTC AACTGGGCAA AGATTGAAAA CAGAGTCCAG CCCTTAGATA 1020 AAGTATAGAT GACAGTGGAA GAGAAGAATG CGAGAGGGTC AGATTCTAAC CAGGCAAGGA 1080 ATGTGACTTG AATCCTCATT CCACCTTTGG CCTGACATTT AATCAGGTCA TTCATCGGAC 1140 ATTCAGATCC ATCTCAATGA CATCTTGTTA TCACATAAGG AGGCCGACAA GGAGTAGGGG 1200 AGTCTCTCCT GATCACCTTT GTTTAATTTC AGATTGAATA TTTTATAAAC AAACTGAAAC 1260 TTATGCCTGA AGAATGTGTG TGAAGCATAA AAAGATAGGT TTAGCAGACC AAGGGCAGAT 1320 ATTTAACTTA AGAGTAATTG 1340
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