Tag | Content |
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EnhancerAtlas ID | HS116-13928 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr16:84088480-84089600 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF14 | MA0740.1 | chr16:84088664-84088678 | AAGGGGGCGTGGCG | - | 6.88 | KLF16 | MA0741.1 | chr16:84088666-84088677 | GGGGGCGTGGC | - | 6.62 | Nfe2l2 | MA0150.2 | chr16:84089568-84089583 | CAGGATGACTGAGCA | + | 6.5 | SP3 | MA0746.2 | chr16:84088665-84088678 | AGGGGGCGTGGCG | - | 6.82 | SP4 | MA0685.1 | chr16:84088663-84088680 | AAAGGGGGCGTGGCGGA | - | 6.16 | SP8 | MA0747.1 | chr16:84088665-84088677 | AGGGGGCGTGGC | - | 6.92 |
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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 |
GH16I084055 | chr16 | 84088921 | 84089607 |
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Enhancer Sequence | CTGCTGCCCT TCCTCCCTGG GATCCCCGCA GACGGATGAT CAGGCCCAGC TATGCTTCTG 60 TCACAACCTA CCGAAGGGAG GCCCAGAGGC GCTCTGTGTT TCTCTAAACA CAAGGGAAGA 120 TGGGCACGTC TCTATCCAGG GGAGAAGGAG GGGCCTGTGG TTCCAGCTGA GTGGGAGGAG 180 GAGAAAGGGG GCGTGGCGGA AGAAGCACCG CTGGCAGTGC CCCGCCTCTG GGAAAGCCCT 240 TCATGGAGGG GACGTGTGGC TGAAAGCCAG GAGAGGCCAT CAGAGGACCC TGGTTCAGAA 300 TGTCAATACG ACTGGGCAAG GCCAAGGGCT CTGGAATTTA CCTTCAGCGC ACCCCGTGAC 360 CTATGCGCAA GGCCCTCAGG ACCCTGGCAC CACCACGTGG TGTCCAGGGC TGGACTGCAC 420 AGACAGGGGT GCCCCTTCCT GATCCCATTT CTGGACAATT CCTGGAACCC AGAGAAACTC 480 CTCTTGGTAG CTATAAACTC TTTGGAAGAG TACAGGGGAC TCTAGAGCAA AAGAACTGCC 540 CAGGCTCGGC TGGAAAGGCC TGGTACCAAT TGCCTTGGGT AGTGGAGAAG AACCTGCCCT 600 AGGCAGTCTA TGTAGCCAGT CAGGATCCCT GGAGAGACAG ACAGGATGAG ACCACCTAAG 660 GGACACACCC CAGCTCAGTC AAGTCCCTCC CAGGGGGGCA GGGCAGAGAA CTGAAGGGGC 720 CTTCTGGGCT GAGGGCTGGG AGCCAGGGCG GCTGCTGCCA TTGGCTGGGA CCCAAACCAG 780 CAGACAGGCA TCCTGTAAGG GACGTTAATA GGTGGCTGGC AGAACTTTCA TAAAGAGCGT 840 GCAAGTTACT TTGAACATGT TTAAGTAGAT CACCCAGCCG TTGTAAAATA AATTCAAATG 900 TGAAAATCTA GGTAGCATTT TCTAAGGGAA ACAACAATCT CTTAATCTGT CAGGCCTGCC 960 CTTGCTCATG CTGGTTTGTG CCACAAAAGA AGCCAAGAGC CAAGGCCACC ACAGCTCCCA 1020 GGAAGGCAGA GACAGGGAGA GTCTGGCCCG CCTCCTGGGG AGGGAGGGAG ACTCCTTTGA 1080 ACAAAATACA GGATGACTGA GCACAATCAC AAAGCAGCCG 1120
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