Tag | Content |
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EnhancerAtlas ID | HS030-04295 |
Organism | Homo sapiens |
Tissue/cell | CyT49 |
Coordinate | chr11:47077260-47078640 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr11:47078040-47078051 | AGTGACTCATC | + | 6.02 | FOXA1 | MA0148.4 | chr11:47077478-47077494 | CTCTATGTAAACAAAA | + | 6.6 | FOXP2 | MA0593.1 | chr11:47077482-47077493 | ATGTAAACAAA | + | 6.14 | JUND | MA0491.1 | chr11:47078040-47078051 | AGTGACTCATC | + | 6.32 | STAT1 | MA0137.3 | chr11:47078245-47078256 | TTTCTAGGAAA | + | 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: 2 | ID | Chromosome | Start | End |
GH11I047055 | chr11 | 47077183 | 47078424 | GH11I047057 | chr11 | 47078561 | 47078896 |
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Enhancer Sequence | TAATATGCTG ATGTGCTATT TCTACTATTT TTACTTCAAT CATTGCCTCT TTGACATATA 60 ACTCTGGAGA TCATGCATCT CCATTACAGT ATTATGAAAG AAGTACTTAG TGTACTGAGG 120 ATCGTATCAT TTCCCTTACA GAATAAATGC ACTAATAGGC AAAAACCAAT GTGGACTCAA 180 TTTTAAGTTA AGTAATTCAG AAAAACTATT CCATTGGTCT CTATGTAAAC AAAACTGGGA 240 ACTGTGAGTA TATAGGTAAA GCTCGTGCTA TGTTATCAGA GGTTATCTTT CCCAGTCCCT 300 CACTCAGTCA GCAAATATTT GTTTTAGACC ACCTAGTACA GTCGTCTCTC AGTCTATGCA 360 GGGATTGGTT CCAGGACCCC TGTTTATACC AAAATCCACG CATAATCAAG GCCTACATTA 420 GTCCTGTGGA ACTCTCATAT GTGAAAAGTC AATCTTCCGT ATACAGGGCT TCATATCCCT 480 AGAATAGTGT ATTTTCGATC CATATTTGGT TGAAAAAAAT CCACCTAAAA GTGTGGACCT 540 GCACAGCTGA AACCTGTGTT GTTCAAGGGT CAGCTGCATG TTGAAGAATA TGGCTAGAGC 600 TAGTTTCTGT GATAGAACAT ATGGAGATAA CTATGGAAAA CAGTCTTCAG ATAGCCTTAA 660 CTTTTTTCCT GATATAGAAG TGGGGCCTCT TCAAGAATGT ATTTACTATC ACGAGGGATT 720 CATATAGCAT TTGGACTCTT AGCAGATGTG GGTTTCTTTA TCTTTCTAAT AGCAGCTGCC 780 AGTGACTCAT CCAGCTGCTA AGAATAAGCA GCTCCAAATT CCCCCAGTTT CTCCTTGTGC 840 CATAAACAAG ACCTAGATTT TATGCTGGCT GTTTATTGTT ATCCTTCTTA ATCAGACAGC 900 CTCAGATTTC TTAGACTAAA TGCAACATCT GTGTCTAGGT GTTCCTAAAA TAATTGGTTA 960 AGTAGCTTTA ATGTATTCTC AGCTTTTTCT AGGAAACTCC AGAACATCTT TCTAAACCAG 1020 AATGTGTCAA TCTCCAATTT TAATCCGGAA TTAGTGAAAA CTCTTGGCGG CAAGGTTCTA 1080 AAGGAAAGGA TTTATTAAGC CCCATTTTAT CAATTATAAT GCCAGGTACC TACCTACTCA 1140 GTGGAACTCC TACTGCATTA TTCTTCTGCA GATAACTTCC TTAGAATGTC ATGTGCATAC 1200 TTTAGCATTA TCAAGTGGAA AGTAACTCTT CTGGGAGGTA GCAAAACAAG AGCATAACAT 1260 ATCTAAAAAT GAAGCCACCT GTAGAACTCT AAGGACCTGG TCCCTTTTGA CAAAAAATAT 1320 TTTATTCCAG TTTTTAGCAA GTACAGGATA TGATATCTTT TCTGCATGAC TGAGTACTGA 1380
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