Tag | Content |
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EnhancerAtlas ID | HS073-02567 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr11:67325280-67326470 |
Target genes | Number: 23 | 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 | TTCTCCTGCC TCAGCCTCCC GAGTAGCTGA GACTACAGGT GTGTGCCACC ACACCCGGCT 60 CTTTTTTGTG TGTTTTTAGT AGAGACAGCG TTTCACCATG TTGGCCAGGC TGGTCTCAAA 120 CTCCTGACCG CAAATGATCT GCCCGCCTTG GCCTCCCAAA ATGCTGGGAT TATAGGCATG 180 AGCCACTGCG CCCAGCCCAA AGTCTTTACA TATTTGCCCA ACATGTATTT AGTTTGGCTG 240 TTTCTTTATT TTAAAAAGCC GCTTTTTATT TAAAGAAAAA CAAAAGATTG TTTTCAGAAA 300 TAAATTCACC TTCCGGGGCT AAAAAAATCC TAACCATTTC CTACTTCTCT TTGGTTCTTG 360 TTCTCACTTC AGGTTGTATA TTAATCAGAT ACAAGTCCCA CTGAGGTTAC AAAGTCCCCC 420 AACCGCAGCA GCTGAAACAA GCTAGAAGTA TGTTTTCACT CTGCAACAAG TCCGGTGTCC 480 TCTGCACGAA GCAATGGGCA CTCCGTGGTG TTAGGGACCC AGGCTCCCCC TGCTCTCTCT 540 GCCATGCCAA GGATGCCATC CCTGTCACGT CCATGTTCCA GCCCCGCGGG ATCAGGGGTT 600 CTCTGAACAA CACCTTTTGA AGAGGCATCT TCTAGGTTTG CAATGTAGAT GATAAAATAA 660 GTCACTTGTT GGCAACACGC AGCATACCCC ATGCAGCACC GGGTTTCTGA CTTGCAACTG 720 GCGTGACTTC TAGTGAATGT GCCGCCCAGA AACACTCGAC GGAGACTACA CTGCTATCAC 780 TAAGTTGTTT TTTCTCCTTC TTGAGTACTT CAGTGGGGTG GGGCCAATTT ATATTTAACC 840 AGTTATTTCA GGAATCAAGG AGGGCGGGGA GGCACACTGA CTGCTGTATT ACTGGTTCAT 900 TCTGGGAAGC CTGGGCCCAG CTCCAGCTTG CTGAGGCCAC GCTACGGGGT CCACAGCGTC 960 GACTGTCCCT GACTCTAACC AGCGTCTCCC AGAGCCTGCA AATGTGCCAC ACACAGCAGC 1020 AGGGGCGGGG CTCACTCCTC ATTCTCACTC TTCGACTTGT ATTGGGCTGA TTTTGATTGA 1080 AAGCAGCAGA AACCCAATCA AAGGCGAATT TGCTGACTCA GTTAACTGGA AGATAACGGA 1140 TGCTTCTGCT TTACGCACGT TGGATCCAGG AGCTCCATCA AATTCTTCAT 1190
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