Tag | Content |
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EnhancerAtlas ID | HS185-00981 |
Organism | Homo sapiens |
Tissue/cell | T98G |
Coordinate | chr1:246795790-246796590 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CEBPA | MA0102.3 | chr1:246796413-246796424 | ATTGCATAATA | + | 6.02 | IRF1 | MA0050.2 | chr1:246796366-246796387 | ACCTTCTTTTAGTTTCTGTTT | + | 6.1 | MLX | MA0663.1 | chr1:246796053-246796063 | ATCACGTGAT | + | 6.02 | MLX | MA0663.1 | chr1:246796053-246796063 | ATCACGTGAT | - | 6.02 | MLXIPL | MA0664.1 | chr1:246796053-246796063 | ATCACGTGAT | + | 6.02 | MLXIPL | MA0664.1 | chr1:246796053-246796063 | ATCACGTGAT | - | 6.02 | Nr2f6(var.2) | MA0728.1 | chr1:246796535-246796550 | GAGGTCAGGAGTTCA | + | 6.22 |
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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 |
GH01I246631 | chr1 | 246794443 | 246797449 |
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Enhancer Sequence | TAGTGGAAGA GTGTATTTTG ACCAAAAGCA GTAAATCTCA AAGCTAGCTT GGTAGCAAGC 60 GAGAGAGAGA GAACTTCTGA GTGATCATGA AGACAAAAAG CTGAACAGTG AGTTTTTCTC 120 TTCCTTTTTT CTGGGTCAGC ATTTAGAGCA TTGCCCAGAG GAAGGTAGGC AGTTGGACAG 180 TGTATCCTGA CCTCACAAGA TGCAGATCTG TGTGATACAA ATGAGAAGGC TAAAGCTCAC 240 AGGATCATTT ACAAAGAAGT AGAATCACGT GATAATAATG GAAATCACTG TGGCAAGTTA 300 ATTGAGTGTT TACAAAAGAC CCATATAAGT TTTTGCCCTG TCATTGTTTA GGCATGTGAT 360 CCTTTGGTCT TGTGGGAGAA AAGCATTCAG TGGGAAATAA TAAGGATCAA GGTGACTTGA 420 AACAGAAACA CTTGACCAGA GAGTCACATA GTTCTTTGAC AGAAAGTAAG GAGAGAAATA 480 AAAAAGGGAA ACATGTAGAT TCCAGGATTC CATGTGGTCC TGTTTCCTTA AATTACTTTT 540 AGTTGACTCC GCAGCAGACA TTCCTTGAGC ATTAAAACCT TCTTTTAGTT TCTGTTTGCC 600 GATAGTGTGG AATCCAAGTA GCTATTGCAT AATATGCCAC ATTAAAATTT ACCTACTTCA 660 AAACCAAGAA ACATTACTAG GCTGGGCGCA GTGGCTCACA CCTGTAATCC CAGCAATTTG 720 GGAGGCTGAG GCAGGCAGAT CGCTTGAGGT CAGGAGTTCA AAACCAGCCT GGCCAACGTG 780 GTGAAACCCC ATCTTGACAA 800
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