Tag | Content |
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EnhancerAtlas ID | HS080-11648 |
Organism | Homo sapiens |
Tissue/cell | H9 |
Coordinate | chr15:31372560-31373450 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF16 | MA0741.1 | chr15:31372819-31372830 | GCCCCGCCCCC | + | 6.02 | KLF16 | MA0741.1 | chr15:31372918-31372929 | GCCCCGCCCCC | + | 6.02 | KLF5 | MA0599.1 | chr15:31372819-31372829 | GCCCCGCCCC | + | 6.02 | KLF5 | MA0599.1 | chr15:31372918-31372928 | GCCCCGCCCC | + | 6.02 | SP1 | MA0079.4 | chr15:31372816-31372831 | CAGGCCCCGCCCCCA | + | 6.56 | SP1 | MA0079.4 | chr15:31372915-31372930 | CAGGCCCCGCCCCCA | + | 6.56 | SP4 | MA0685.1 | chr15:31372816-31372833 | CAGGCCCCGCCCCCAAG | + | 6.3 | SP4 | MA0685.1 | chr15:31372915-31372932 | CAGGCCCCGCCCCCAGC | + | 6.4 | Zfx | MA0146.2 | chr15:31372816-31372830 | CAGGCCCCGCCCCC | - | 6.19 | Zfx | MA0146.2 | chr15:31372915-31372929 | CAGGCCCCGCCCCC | - | 6.19 |
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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 |
GH15I031079 | chr15 | 31371436 | 31376284 |
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Enhancer Sequence | CACATCGCCT GTCATGGAAC AAATATTTAT TATGAGGCTC TGGATAAAAC GCACCAAGAG 60 GAACAAAAGT GCCCAAAGTA CATCATCTGA ACCTGATCTG GAGGAAGGAT CATCAGACAG 120 CCCGAACTGA GGGCCATCCT ACGAAATAAC CCACCTGCGT TCCTCAAAAA CGTCAAGGCC 180 ACGAAAAGAC AAGGAAGAAC TGAGGGAAGA TTCCAGAGGC TGGACACAAG ATCTGGCACT 240 GTCCTTCCCT AGCCCCCAGG CCCCGCCCCC AAGTCCGCCC CCATCGTCCT CGACCCCGCC 300 CCCTCACCCC GCCCCCTGTT ACCTCTCACG GTCCCGCCCT CTCAGCCCGG TCCTCCAGGC 360 CCCGCCCCCA GCCCCGCTCC CTCTCATAGT CCCGCCCCTC GTCCTTTCCC ACACTTTCCC 420 TGGCAGCCCC TCTCACCGCC CTAGGATAAG AAACCCGCGC TGGGGCGCTG TCCAGGAAAC 480 CTGTGCCAGC ACAGCGTGGG GAATCAGAAA CTAAAGCCCA GGCTCCGAGC GCTTAGGCTC 540 AGGCCCCTCA TCGTGAAAGG GGGAAACGCA GCCTGCCCTA CAGGACTTAA TGCCACCGGC 600 GGATGAGGGA GCAACAACGT GCCCCTCGCT GGCTTTTGTG GCTAAGTCTG TTCCATCACA 660 AGGGGTGTTT AGATGCCTCC TTCAAGGCAG GGCCCCCTGT CCCCCCCCTT ATCGTGCCAA 720 TGAAGGTCAT CTGTGATGAC TCTGGGGCAT CGGTCTTGCA TTTTGTCCCC CAGATTCCGA 780 AAAGGAGGGC TTTTCATGGT GCCGAGTGCC AGCCCTTGCT GTGGCTCGGC ACCAGGGCAA 840 GTGCAACTGG CGCCATGGCC CGAGCCAGGC TCAATCCACT TCCCTCTGCT 890
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