Tag | Content |
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EnhancerAtlas ID | HS044-02906 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr11:130272560-130274060 |
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) |
Myog | MA0500.1 | chr11:130273217-130273228 | CTGCAGCTGTT | - | 6.02 | Tcf12 | MA0521.1 | chr11:130273217-130273228 | CTGCAGCTGTT | - | 6.62 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_08530 | chr11:130270251-130275391 | Brain_Inferior_Temporal_Lobe | SE_39023 | chr11:130269984-130274795 | IMR90 | SE_69174 | chr11:130270939-130272821 | H9 | SE_69174 | chr11:130272967-130276303 | H9 |
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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 |
GH11I130400 | chr11 | 130270005 | 130274950 |
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Enhancer Sequence | GTTTTGTTTT TTGGGGGGTG TGGGGAGGGA GGGGTGGTTT GAAACAACTC CGGAGCACAC 60 TCCAGAGGAA AACAGGAAGG GTGACATGTT TGGACACCAG AAAAGAGGAA GAGTCCTCAC 120 TAAGAGGGTG ACTTGGTTAA AAAGTTCAAG CACAAAGGAT GTAGAAGCAG GTGGATGTCA 180 TCAGAGAACA GATGCGGATC TAGTGAGATG GGTCCTACCA CCCCTGGAAT ATGTTCCTGG 240 GAGAGGGGTG GTCTGCTAGA GTGGACTGGG AATAGTAATA TTGCATACTT TTGTAAATTC 300 ACAAAACCCT CTGATCTGTG ATAGAGGAAT AAAGGGCAGA GGATAAACCC CAGATAAAGA 360 TTCACTTATC TTAAAAATGA AAGGTTGGAA ATTAACTTTA TGCTACTGTA CCACCTTCGA 420 AGTATTTCTG GCAGGTGCCT GGAGGATTCA GATTAATGAC CAAATTACCT GCCAAGTCAG 480 GGCCTCCCAT TAGAAGAGAG TACCAGTTTC CATTAGGAGC ACTAGCTGGA AAACACAATC 540 TTTCAGCAGA GGAAATACAG TCTTCTCTCC TTCTCTGGGT GCACAGAGTG GTCGTGGTTG 600 GCTGGGGCAG ATAATGGTGT GGTCTTCCTC TGCAGATCTG GTTTCTGAGT CCCTGGGCTG 660 CAGCTGTTGA ATTTCCAGAC ACAAACAAGT ATGCGTTCTG AGAGCCTCGC CGAGCCCACA 720 CAACCGGGAG AGCCAAGCTG GATTCCATTC TGCTTTGCAC ATCAGCAGCT CTGCTGCCAG 780 CTGAACTCCA GGGCAAAAGC TGTGCCTGGT AATGATGCAG GCAGCAGGGA TGGCACAGCT 840 GGCCTGGCTT AGGCCGTTAA GGGGGACACG CTTGGCCTTA TTTGGGGGAG AGCGAGAAAT 900 GGAAGGCGAT GAAGAGTTGC GGAAGCATAC ATCAGCCTCC ACAAAACTGG TGCACAGCAG 960 GGAAACAATC TGGTTTTGCT AGTCATCAAC AACATGCCTG TGTGTGTGCC TGTTTATGCT 1020 TAGGTAAGCC CAGCCTCCCA CTCGCTGAAA AGAGTAGGCA GACAAGAAGG AGTGACCAAC 1080 TCTGAGTCAG CTGTCATCGT GTAGAGAGCA GCTAAGGGGA ACAGTGGGGC TGGAATCTCA 1140 TGGCCTTGCC TAGTGCCCCT ACAGCATCCT CTCTGCCCAT GGTGCCAGAT ATCTGAATGG 1200 GAGGACAAAG GGGGCACAGG TGGTGAAAAA AACCAAGATG CACATTTGGG TATTTTCCTT 1260 CTTTTGCTAG AATGTCATTT CTTGATGTCT GTTTCTTGTC ACCCATTTGT GATCAGGGAC 1320 TAAGTAAGTT CCCTCTGCAC CAGACCAGGT GGAAGACTGA GCCAGAGTTC CTCTGAGCCA 1380 CAGGAGAGAT GAGGAGCTAT GGAGCGGAGT AGGGGCTGAG GATCTGGTGC CCCCAGCTAA 1440 ACTAAAAGGA GGCAGGCAGC ATGTAAGAGG ATGATGGGGT AGCTCACAGA GAGGAAGGGG 1500
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