Tag | Content |
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EnhancerAtlas ID | HS164-02619 |
Organism | Homo sapiens |
Tissue/cell | Raji |
Coordinate | chr11:119437920-119440340 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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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 | Nr2f6(var.2) | MA0728.1 | chr11:119438248-119438263 | TGAACTCCTGACCTC | - | 6.22 | RELA | MA0107.1 | chr11:119438566-119438576 | GGGAATTTCC | + | 6.02 | RREB1 | MA0073.1 | chr11:119438713-119438733 | GCATTGGGGGTGGGGGGTGG | - | 6.03 | TFAP2A | MA0003.3 | chr11:119438275-119438286 | CGCCTCAGGCT | + | 6.14 |
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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 | GGGGCCTTTC CAGAGGGATG GACTAGCCTA AATGTCCAGA AAAGAAGTGA ACCAGACTCT 60 TGATTTTTGA GATTTTGTGT GTGTGTGTGT GTGTGTGTGT GTGTGTGTGT GTGTGTGTGT 120 GTGTTTGAGA CAGAGTCTCA CTCTATCGCC CGGGCTGGAG TTCAATGCAC AATCTTGGCT 180 CACTGCAACC TCCACCTCCT GGGTTCAAGT GATCCTCTTG CCTCAGCCTC CTGAGTAGCT 240 GGGACTACAG GCGTGTGCCA CCACGCCCGG CTAATTTTTG TATTTTTCGT ATAGAGATGA 300 GGTTTCACCA TATTGGCCAG GCTGGTCTTG AACTCCTGAC CTCAGGTGAT CCACTCGCCT 360 CAGGCTTCCA AAGTGTTGGG ATTATAGGTG TGAGCCACCG CACTCGGCAT TTTTGAGAAT 420 TTAGGAGATT AAGCACCTGT TCCCCACCCC TTGGGGTTTT GAAAATTAGG TGGGAAGAAG 480 CTGATTCTAG GTTTTGCAAG TAAAGGGGGA CCTAGTACTG CTGGGGCCAG CTTGCACCCA 540 GGAAGTGGCT GGTAGCTGAG CAGAATGAGC CACTGATGAC AGCTTTGGCT CTTTGGCCTT 600 AGGCCTAGTG GGTCCCCAGG GTTCTGCTGA TCTGAGCATT TTGCTGGGGA ATTTCCCTTT 660 TCTGAAAGGG CTCCACAATA AGGTGGTGGC ATCAGCTGGG GCCTAGGCCA GGCACCTTCT 720 GTCTATGGAC TCTGGCCTGA GTTTCAGGGA CATCTTGACT CACAAGGGGA GCTTTTCCCT 780 CCCACCAATC ATGGCATTGG GGGTGGGGGG TGGGCAGCCA CCCTGGATAA CGTCACTCAG 840 TGCATACCAC TGCTGGCCCC TGTGGCTGTT GCATGAAGAG GAGACGGGGC TCCATTTTCC 900 AGAAATCGTC TGTGCTAGGC ATCCCAGTGA GGGGGCTGAG CCAACCTCTA AGTTTCCTCT 960 AAGACACTAG GAAGCATTGG GGGAACCCTG GATGCACCCA AGCAGGGACT GGATGGGGGA 1020 GGCTTGAGCA TTCGCTCTTT TCTCCCACAT GGGTTGGAGG CCACTCTGCC TCATTATCGT 1080 CCTCTACATT TGCATGACTG CTGTCCTGTG AAAAATCTCC GCTTGTGAGC CAGCACAAGT 1140 ATGACTCAGC ATGTCTCTTT AATTCCCTTC GGGCACGACC ATCAGAGTCA GTTTACAATA 1200 ACCAGACGCC TGGCTTTACA ATCACTCCTC ATTGTTGACC CAAAACAGCA TCCTGCAGCT 1260 TGATCATTGC CCATGTGCCA GACTTCTCTC AGAATGACTC TTATTTAAAA AAAAAAAAAA 1320 ATCACATCTG GTCCATTTAG TGGCCTAGAG CACATACCCT TGAGAATTCA TCAAGGCAGA 1380 AAGTATTTGT TATTCGAGGA TGGGTTTGAT TTTTGGCAAT GATGTTGAGG CTCTCTGAGT 1440 CAAGTCTGGA GGATTATGCA GCAGGGAGAG CTCTTTGCTT AGACCACTGC ATCAGACCAC 1500 CCTCCTCAAT CTCAGGGCTC AGCTACCACT TCCCTTCTAT AGCTCCCCCA GTCGCCATGG 1560 CAGATGTGGC CAGACACCTC ACTCTCTTGC CATCCGCCCA GGGTTTCTCT GACACCAAGG 1620 CCATGCCCGC CTCTTCCTTG TCTCAGGTGC ATTTTGCATG GTTCTTCAGA GGTTCCCTAG 1680 CAGGATGGAG CCTCAGTGAC CCACAGTGAT GACCAGCTCA GTTAAGAAAA CTTAGCTTGG 1740 CCTTTCTGCT TCCCTGTTTT ATGCTTCCCA ATCCCCCTTG GGATTCTAGG GAACCATTGC 1800 TTTTCCCTAG AATCTCTTTC CAAAATAAGC TACTTGAACC AAAGGCTCTT TATGTGGGGG 1860 AACCCAGGCA AGGACAGCTG CCCTGCTGAA TTTTTTGTAA GATTTCAACA GAGCTTGAGG 1920 ACGGAGTTGG GGGGAGTCTA TTGAGATACT AGGTCATAGG AATTCATAGT GTCCCGTGGC 1980 ATCATATATA TGGGCCATCT CTTTTGCTCT CTCTCCCCCT TTTTTAAAAA ACAGTTTTTT 2040 TTAGATATAA CTCACCTACC ATATAATTCC CATTTAAAGT GTGCAATTTG GCCAGGCATA 2100 TGGCTCATGC CTGTAATCCC AGCACTTTGG GAGGTGGAAG TGGGAGGATT GCTTGAGTCC 2160 AGAAGTTCAA GATCAGCCTG GGGAATACAG TGAAACCCCA TCTCTATATA TAAAAAAAAA 2220 TAAAGTGTGC AATTCAGTGG TTTTTAGTAT ATTTACAGAG TTGTGCACCC ATCACTGCAT 2280 CAATTTTAGA ACATATTTAT CACCCCTAAA AGAAACACAG TACTCATTAA CAATCACTCT 2340 CCATTTCTCC CACAACCTCA TCCCTCTAGG CAACCACTGG TCTACTTTTT GTTTGCCTAT 2400 TGTGGACATT TCACTTAAAT 2420
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