Tag | Content |
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EnhancerAtlas ID | HS094-08177 |
Organism | Homo sapiens |
Tissue/cell | hMADS-3 |
Coordinate | chr11:119438310-119439830 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFE2L1 | MA0089.2 | chr11:119439058-119439073 | GTATGACTCAGCATG | + | 6.73 | Nfe2l2 | MA0150.2 | chr11:119439056-119439071 | AAGTATGACTCAGCA | + | 7.48 | RELA | MA0107.1 | chr11:119438566-119438576 | GGGAATTTCC | + | 6.02 | RREB1 | MA0073.1 | chr11:119438713-119438733 | GCATTGGGGGTGGGGGGTGG | - | 6.03 |
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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 |
GH11I119567 | chr11 | 119438347 | 119439690 |
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Enhancer Sequence | TGAGCCACCG CACTCGGCAT TTTTGAGAAT TTAGGAGATT AAGCACCTGT TCCCCACCCC 60 TTGGGGTTTT GAAAATTAGG TGGGAAGAAG CTGATTCTAG GTTTTGCAAG TAAAGGGGGA 120 CCTAGTACTG CTGGGGCCAG CTTGCACCCA GGAAGTGGCT GGTAGCTGAG CAGAATGAGC 180 CACTGATGAC AGCTTTGGCT CTTTGGCCTT AGGCCTAGTG GGTCCCCAGG GTTCTGCTGA 240 TCTGAGCATT TTGCTGGGGA ATTTCCCTTT TCTGAAAGGG CTCCACAATA AGGTGGTGGC 300 ATCAGCTGGG GCCTAGGCCA GGCACCTTCT GTCTATGGAC TCTGGCCTGA GTTTCAGGGA 360 CATCTTGACT CACAAGGGGA GCTTTTCCCT CCCACCAATC ATGGCATTGG GGGTGGGGGG 420 TGGGCAGCCA CCCTGGATAA CGTCACTCAG TGCATACCAC TGCTGGCCCC TGTGGCTGTT 480 GCATGAAGAG GAGACGGGGC TCCATTTTCC AGAAATCGTC TGTGCTAGGC ATCCCAGTGA 540 GGGGGCTGAG CCAACCTCTA AGTTTCCTCT AAGACACTAG GAAGCATTGG GGGAACCCTG 600 GATGCACCCA AGCAGGGACT GGATGGGGGA GGCTTGAGCA TTCGCTCTTT TCTCCCACAT 660 GGGTTGGAGG CCACTCTGCC TCATTATCGT CCTCTACATT TGCATGACTG CTGTCCTGTG 720 AAAAATCTCC GCTTGTGAGC CAGCACAAGT ATGACTCAGC ATGTCTCTTT AATTCCCTTC 780 GGGCACGACC ATCAGAGTCA GTTTACAATA ACCAGACGCC TGGCTTTACA ATCACTCCTC 840 ATTGTTGACC CAAAACAGCA TCCTGCAGCT TGATCATTGC CCATGTGCCA GACTTCTCTC 900 AGAATGACTC TTATTTAAAA AAAAAAAAAA ATCACATCTG GTCCATTTAG TGGCCTAGAG 960 CACATACCCT TGAGAATTCA TCAAGGCAGA AAGTATTTGT TATTCGAGGA TGGGTTTGAT 1020 TTTTGGCAAT GATGTTGAGG CTCTCTGAGT CAAGTCTGGA GGATTATGCA GCAGGGAGAG 1080 CTCTTTGCTT AGACCACTGC ATCAGACCAC CCTCCTCAAT CTCAGGGCTC AGCTACCACT 1140 TCCCTTCTAT AGCTCCCCCA GTCGCCATGG CAGATGTGGC CAGACACCTC ACTCTCTTGC 1200 CATCCGCCCA GGGTTTCTCT GACACCAAGG CCATGCCCGC CTCTTCCTTG TCTCAGGTGC 1260 ATTTTGCATG GTTCTTCAGA GGTTCCCTAG CAGGATGGAG CCTCAGTGAC CCACAGTGAT 1320 GACCAGCTCA GTTAAGAAAA CTTAGCTTGG CCTTTCTGCT TCCCTGTTTT ATGCTTCCCA 1380 ATCCCCCTTG GGATTCTAGG GAACCATTGC TTTTCCCTAG AATCTCTTTC CAAAATAAGC 1440 TACTTGAACC AAAGGCTCTT TATGTGGGGG AACCCAGGCA AGGACAGCTG CCCTGCTGAA 1500 TTTTTTGTAA GATTTCAACA 1520
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