Tag | Content |
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EnhancerAtlas ID | HS074-02673 |
Organism | Homo sapiens |
Tissue/cell | GM19239 |
Coordinate | chr11:67325510-67326500 |
Target genes | Number: 21 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF5 | MA0599.1 | chr11:67326301-67326311 | GGGGCGGGGC | - | 6.02 | MAFK | MA0496.2 | chr11:67326387-67326406 | ATTTGCTGACTCAGTTAAC | - | 6.17 | Mafb | MA0117.2 | chr11:67326386-67326398 | AATTTGCTGACT | + | 6.22 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_28422 | chr11:67325001-67327956 | Fetal_Intestine |
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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 |
GH11I067557 | chr11 | 67325001 | 67327741 |
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Enhancer Sequence | AGTTTGGCTG TTTCTTTATT TTAAAAAGCC GCTTTTTATT TAAAGAAAAA CAAAAGATTG 60 TTTTCAGAAA TAAATTCACC TTCCGGGGCT AAAAAAATCC TAACCATTTC CTACTTCTCT 120 TTGGTTCTTG TTCTCACTTC AGGTTGTATA TTAATCAGAT ACAAGTCCCA CTGAGGTTAC 180 AAAGTCCCCC AACCGCAGCA GCTGAAACAA GCTAGAAGTA TGTTTTCACT CTGCAACAAG 240 TCCGGTGTCC TCTGCACGAA GCAATGGGCA CTCCGTGGTG TTAGGGACCC AGGCTCCCCC 300 TGCTCTCTCT GCCATGCCAA GGATGCCATC CCTGTCACGT CCATGTTCCA GCCCCGCGGG 360 ATCAGGGGTT CTCTGAACAA CACCTTTTGA AGAGGCATCT TCTAGGTTTG CAATGTAGAT 420 GATAAAATAA GTCACTTGTT GGCAACACGC AGCATACCCC ATGCAGCACC GGGTTTCTGA 480 CTTGCAACTG GCGTGACTTC TAGTGAATGT GCCGCCCAGA AACACTCGAC GGAGACTACA 540 CTGCTATCAC TAAGTTGTTT TTTCTCCTTC TTGAGTACTT CAGTGGGGTG GGGCCAATTT 600 ATATTTAACC AGTTATTTCA GGAATCAAGG AGGGCGGGGA GGCACACTGA CTGCTGTATT 660 ACTGGTTCAT TCTGGGAAGC CTGGGCCCAG CTCCAGCTTG CTGAGGCCAC GCTACGGGGT 720 CCACAGCGTC GACTGTCCCT GACTCTAACC AGCGTCTCCC AGAGCCTGCA AATGTGCCAC 780 ACACAGCAGC AGGGGCGGGG CTCACTCCTC ATTCTCACTC TTCGACTTGT ATTGGGCTGA 840 TTTTGATTGA AAGCAGCAGA AACCCAATCA AAGGCGAATT TGCTGACTCA GTTAACTGGA 900 AGATAACGGA TGCTTCTGCT TTACGCACGT TGGATCCAGG AGCTCCATCA AATTCTTCAT 960 CATTTCTCAC TCTTCCTCCC CATGAAACAT 990
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