Tag | Content |
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EnhancerAtlas ID | HS180-36935 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr4:89888600-89889790 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Mecom | MA0029.1 | chr4:89889275-89889289 | AAGAGAAGATAAAA | + | 6.05 | Sox6 | MA0515.1 | chr4:89889517-89889527 | CCATTGTTTT | + | 6.02 |
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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 |
GH04I088966 | chr4 | 89887973 | 89891286 |
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Enhancer Sequence | AAATACACCA AATTCGTTTA TGAGCACGTT TATTGGTAAG TTCCATGTGG AACATTTTAA 60 CTCTTGTAGT GGGTAGCTGC AAATATATTC AGGGTCTTCA TATTTATCTT AATTTATAAT 120 GTGAGCCCAT TGTGGGATGC GGCTTAAGGA GAGTAGCCTT ATCTTTGCTC ATCATAGAAA 180 TGAGAGAGAA TTCCATGTGC CTTACAACAC AGAAAAGATG CCCGGCAAGA GCAATGGGTA 240 GAAAACTCAG TGGGTCAAGC ACTGTACCAT CATAATTAGA AAAACAAATA AACCAAACTT 300 TAATCAGCAG TTCAGTTATT CCCACTGTGG GCAGGAGGTT GGTAATGGGG ACAGAGAGGA 360 AGGGAAATTC TTTTGGAGAT GAAATCAGTT GATACTTGTT TATTACCAGG AGTTCCATGC 420 TTGTTTTTCC GGGTATCACG TCTCTTAAAC AGTGCCTAGT GCTGCCATGT GGAGGACACT 480 GGCTGAGTGA GACAGGCTGT GGTGGTAGTG TGTGTGTGTT TACTTTCCAC AATTACAGTC 540 CACAGTCATA CTGACTTTTC CTGTTTATCC CTTTCCACAG AAGACCTGCC ATAATTTGCA 600 GAGTCTAGCA AGTAGTTAGA AAGGTTTGTT GACTAAATGT GGAAGATTGG TAAGCCTCTG 660 GGTACAATGG CCAAGAAGAG AAGATAAAAA GAACTATTTG CATTATCTCT GATACAAAGC 720 ACCCGCCTCA GGGACTTGAA TATCCTAGTT ATTAAAACTG CATTCAACTC TTGGCCACAT 780 CACCTACTTG GAAACAAAGG TCATCATCTG ATTAAGAAAT ACTTTTCCTC CTGTTTGCTC 840 AGAACACACC TTCTAAAGTT TCAACTTTGC AACACTTATG TTCTAAACAA TTAGGGATAA 900 AAGTAGAGGC CAAACAACCA TTGTTTTCCA ACATAGCAAG TACAAAAATA TATAATCAGT 960 AGCAAGGTAA AATTGACTCT GAAAAAAGCT TTCAAATTCT TTCTTCGCTA TGACCGAGAA 1020 TCAGGAGGGG ATACAGTAAT TACTTACTCT ACAATGATTT TGTTTTCAGT TTAGAGTACT 1080 TGGCAATTGT TCATAATCTT TTTTTCTGCC CTATATGCCC CAGAGGATAT ACACTGTTCT 1140 TTCTTAATAA CAAGGGAATC ATAGACAATA ATTTCCAAAA GTGTTTTGGA 1190
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