Tag | Content |
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EnhancerAtlas ID | HS101-01135 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:35289810-35292020 |
Target genes | Number: 14 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFIL3 | MA0025.1 | chr1:35290591-35290602 | TTATGTAACCT | + | 6.14 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 35290944 | 35291068 | chr1 | 35291146 | 35291505 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I034825 | chr1 | 35290806 | 35291667 |
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Enhancer Sequence | TCCTGGCCCT ATACTTGAAC CTACATCTTT ACTTCCTGTT ACAATCCTGA GTCTACAATC 60 ATGGATGAGC CAAATCTCCA CCAGCAGTCC AGGATGTTAA GTAGCACATC TTTATCGCTA 120 GGGAGGGAGG CACAACCAAA TGAACATGGC TTGGTGTTTC AAAGACCTAG ACTGAAATCT 180 CTGCTCTACA AATTACAAAT CACATGCCAA GGCCATGTGA TACCATCTCT CTGAGCCTCA 240 GTGTCTGAGC CTCAGAGCCT TATAGATAGG CCTCAGCCTA TCTATAAGAT GGGGATAATA 300 ATGTCTTCTT CACAGAGTTG TTGTGAAGAT TAAACTAGGT AATGGATGTG TAAGGACCCA 360 GCATAGCGTC TGACACACAT GAGTCTCTTG GTAGACCCAG AACTACTTTC CCAATTCCCA 420 AAGAATACTA GAGCTGACCA GGCTCCCAGG GGCCAGCATA CCATACAGAG GCCTGTGGAT 480 AAGTACAGGG ATGCACCTTC AGCCCCAGTA GAAGTGGCAT CTGCTCAGCT CTCTTTCCTG 540 TACCCCTGGA AGCAAAAGTA AGTACAGACC TCTTACTTGA AATACTGTAA CAACCTCCTC 600 TAAATCACAC ACTGACAATA CCACCACCAA CAGCAACAGT CTAATGATAG CTAAAATCTA 660 TTGGGTTTAT TGTGTTGTAC ACTCCCCATG AGAAAGTTGA GATGCTAGAA GCACATTTAA 720 TTTTCACAAT AATTCTATAA GGTACATATT CTACAGATGA GGAAAATAGG GCCCAGAGAG 780 GTTATGTAAC CTGCTGAAAG TCACACAGCC ACCAGGTAGC ACAGCTAGAA ATTAAACGTA 840 TTCATATGTT CAATCTTTCA TTGATTGGGT CAAGAAATTG TTTCTGCCAC ATGCCCTGTG 900 CCAGGTCATA CACAGGGCCT GAAGACACAA AGGTGCAGAG ACACAAAATC CTCAAGGTGC 960 CCCAGGGGAA ACAGATCATG ACTCATTAGC AACAGTCCCA TGCAGAATGC AGCCTGTGCC 1020 ATGCCAGTCC CACTCTGGCC CCTTCCCCCA GCTCTGCTGC CTCCAAAAGC TGTGGAACCC 1080 CAGCAACAGC CCAGAGACGC TTCCTGAGAC CGCTGTTTTC CTTGGCCCTG AGGTGAGAGA 1140 CAGTGTGCCC AACAAGGTGG AAAACAAGAC AGTGGGTGGG GGAAGTAAGA GGAGAGCAAA 1200 TCTCCCCACC CAATCAACCT GTCTCTGTCA CTGGTGGAAG CAGGGATCAG AGGGGGCTGC 1260 CTTTCCACCC ACCCACCAGC CCGTCCAAGC CATTGTTCCC TTGTTGTGAC AGGGGGTTCA 1320 ACTGGAGCCC ACGGACTGGG GGCTTCCTCC CCAGCTCGCC GTGCTTGGAC AGCTGGAGGA 1380 AACAGGCGGC TGGCGGGCCA GCTCTCCACT CCAACAACAA CAGGCTGCCC GCCCACTGGC 1440 GGCCTTGCTG GGGGCCCAGC CTGGAGCCAG AGAGGCCACC CCACTCCACC CCATCACTGG 1500 CAAAACATGT TTTCTTGTTT TCTGAAGGGG AGGAGGAGGA CTGTACCCAT GCTGAGCAAA 1560 CACAGGCACT GATAAGCATG GACAGGCCTG GCTGCCAGGT GGGGCTGCAG AGGCAGGGCC 1620 AGGACCAGGC TGGCCCCGGA GGTCATTCTG ACCAGCCTGC CAGGTTCAGA GTCAGGTTGG 1680 GGGACAGAAA GCGCCTGCCA CTCCAGGGAT AAAGCACCCA GCCACAAGCC TTTCAGAGAA 1740 AGAGAAGAGA CTGCCAGGCC ACAGACCTCA GAAGCACAGC AGGCTAGCCT TCAAGAGCTG 1800 GAACGCTCTA TCAGGTGCCT GCTCCTCAGC CAGTCTCTAT GCCAGTCCCT TTGCCAGCTA 1860 TTAATATCCT TTTCAGTGCT TGTAGAGACC ATGAGAAGTA GGGACTGCTG CCCATGGCCT 1920 TCTTCAGATA AGGAAACTGA GGTTTAGAGA GGCTGAGTGA CTTGTTCAAA GTCACACAGC 1980 AATTGGTACC CAGTTGGGAT ATTAATTTTT ATCTGTCTGA CCACAAAGTT CATGTGCTTT 2040 TTACCATGCC CTGACCAGTC CCAGAGCCCT TTATATTTGT AGGAGTCTTT AGTTTACAAA 2100 GCACTTACCA GGTTACTGTA TTAGTTTCCT AGAGAGCTGC TGCAGAAACC ATCATCAACC 2160 TGCCAGAGCT GTATCTCTTA TCAAAAAGCT CACAATAGAT CAGTTAGGTT 2210
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