Tag | Content |
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EnhancerAtlas ID | HS080-36662 |
Organism | Homo sapiens |
Tissue/cell | H9 |
Coordinate | chr9:23537170-23538220 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EBF1 | MA0154.3 | chr9:23538015-23538029 | GTTCCCTGGGGACT | - | 6.41 | ZNF263 | MA0528.1 | chr9:23538135-23538156 | TTCTCCGTCCCCCACTCCTTC | - | 6.17 |
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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 |
GH09I023537 | chr9 | 23537599 | 23538198 |
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Enhancer Sequence | ACCCACAAAG AACTGAACAA GACAGGGCAC CAAAGCCACT CAGCTGACTG TCATCTTGAA 60 ATTATGGATT CTGTGTCCTA ATTTATCACC CTCATTCTGT TCTAGCCTTT CTGATGCTTG 120 GCATTAATTT TCCTTTTCTG AGCACTGACC CCACCTCTCC TATTCTATTC CTCCACTGTT 180 GAACCGGAAC AAAGGTCACT TGAAAGCGAA GCAAAACTCA GCTGTTACCA AAGGCGCAAA 240 GATCAAAGTT GGCAGCTACG CTAAAGTTCA GGATTCAGAG ACTTCCTCTT TAAGATCAAA 300 ATTCCAGATG ATCCAAATAT AGGCAAATGA GCCCCAGTAG AACACTCAGC TTTCTGTGCT 360 GAATCCAGGA AAGAAGCAGA AATCACCATA GAAGCAACTC AGTTTCACTC TTTGCAACCC 420 CGTGGGCTCT ATGCTAATTG CCTACCCCAA GAGTGAGATC GCATTTCAAA ATATGGTCAA 480 ACGCAAAACA GCCAAGTCAA TCAAGCATTA AGTATTCAAG CACAATTATC CGAACACATG 540 CCCAAGGACC AGCAGTGAAG CAGCTTAATT TGGGAGCGGC TCCGTAATCA TCTCTCCGGG 600 CAGCTGAGAT TTTAACCTCT CCCCTCGGGC CTCCTGTTCG GGGCACTAGG CTAGCTCTCT 660 CTGTGTGAGA GATCACAACG GGAGCCGCTG CCCCCCAGTT GTGAGGCTTC ATTTAAATTC 720 ATGCTAAGGG TAAGGGAGGG GGAGGGGGCA GAAGGTCTGC AGAAGCCCCC ATTGTTGGGG 780 AGAGACGTGT GGGAGCAGAT GGTCTGGCTG GTCACTCAGT CTGGCTGTCA GATGCTCTCT 840 GTCAAGTTCC CTGGGGACTG CAGGGTTTTC TTTCCACTCT CCGCTCTGGT CATATGTGTT 900 TGCTCAGCGT GAGCGAGGGG TCTTTTTCTT TATCACCCCT CAGACTTCCA GGGGGCTGAG 960 TTGCCTTCTC CGTCCCCCAC TCCTTCCCTC TGCTTTCTCT GCTTTTTCTG GACCAGCTAG 1020 TGCCGCGCCT CCAAGGGCCC GCTCGCTGCA 1050
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