Tag | Content |
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EnhancerAtlas ID | HS092-10628 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr11:119438400-119439660 |
Target genes | Number: 20 | Name | Ensembl ID |
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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 | CTGATTCTAG GTTTTGCAAG TAAAGGGGGA CCTAGTACTG CTGGGGCCAG CTTGCACCCA 60 GGAAGTGGCT GGTAGCTGAG CAGAATGAGC CACTGATGAC AGCTTTGGCT CTTTGGCCTT 120 AGGCCTAGTG GGTCCCCAGG GTTCTGCTGA TCTGAGCATT TTGCTGGGGA ATTTCCCTTT 180 TCTGAAAGGG CTCCACAATA AGGTGGTGGC ATCAGCTGGG GCCTAGGCCA GGCACCTTCT 240 GTCTATGGAC TCTGGCCTGA GTTTCAGGGA CATCTTGACT CACAAGGGGA GCTTTTCCCT 300 CCCACCAATC ATGGCATTGG GGGTGGGGGG TGGGCAGCCA CCCTGGATAA CGTCACTCAG 360 TGCATACCAC TGCTGGCCCC TGTGGCTGTT GCATGAAGAG GAGACGGGGC TCCATTTTCC 420 AGAAATCGTC TGTGCTAGGC ATCCCAGTGA GGGGGCTGAG CCAACCTCTA AGTTTCCTCT 480 AAGACACTAG GAAGCATTGG GGGAACCCTG GATGCACCCA AGCAGGGACT GGATGGGGGA 540 GGCTTGAGCA TTCGCTCTTT TCTCCCACAT GGGTTGGAGG CCACTCTGCC TCATTATCGT 600 CCTCTACATT TGCATGACTG CTGTCCTGTG AAAAATCTCC GCTTGTGAGC CAGCACAAGT 660 ATGACTCAGC ATGTCTCTTT AATTCCCTTC GGGCACGACC ATCAGAGTCA GTTTACAATA 720 ACCAGACGCC TGGCTTTACA ATCACTCCTC ATTGTTGACC CAAAACAGCA TCCTGCAGCT 780 TGATCATTGC CCATGTGCCA GACTTCTCTC AGAATGACTC TTATTTAAAA AAAAAAAAAA 840 ATCACATCTG GTCCATTTAG TGGCCTAGAG CACATACCCT TGAGAATTCA TCAAGGCAGA 900 AAGTATTTGT TATTCGAGGA TGGGTTTGAT TTTTGGCAAT GATGTTGAGG CTCTCTGAGT 960 CAAGTCTGGA GGATTATGCA GCAGGGAGAG CTCTTTGCTT AGACCACTGC ATCAGACCAC 1020 CCTCCTCAAT CTCAGGGCTC AGCTACCACT TCCCTTCTAT AGCTCCCCCA GTCGCCATGG 1080 CAGATGTGGC CAGACACCTC ACTCTCTTGC CATCCGCCCA GGGTTTCTCT GACACCAAGG 1140 CCATGCCCGC CTCTTCCTTG TCTCAGGTGC ATTTTGCATG GTTCTTCAGA GGTTCCCTAG 1200 CAGGATGGAG CCTCAGTGAC CCACAGTGAT GACCAGCTCA GTTAAGAAAA CTTAGCTTGG 1260
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