Tag | Content |
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EnhancerAtlas ID | HS007-04113 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr12:109143940-109145000 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr12:109144973-109144984 | GGTGACTCATG | + | 6.62 | JUND | MA0491.1 | chr12:109144973-109144984 | GGTGACTCATG | + | 6.02 |
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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 |
GH12I108750 | chr12 | 109144065 | 109144865 |
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Enhancer Sequence | ACTCACTCTG TCACCCAGGC TGGAGTGCAG TGGCATGATC TCGGCTCACT GCAACCTCTG 60 CTTCCCGGGT TCAAGCAATT TTCCTGCCTC AGCCTCTCAA GCAGCTGGGA CTACAGGCGT 120 GTGACACCAT GGCCAGCTAA TTTTTGTATT TCTAGCGAAG ATGGAGGGTT TTGCCAGTTT 180 TGCCATGTTG GCCAGGCTGG TCTCAAACTC CTGACCTCCC GCCTCAGCCT CCCAAAGTGC 240 TGGGATTACA AGCATGAGCC ACCATGCCTG GTCAAGTTAT ATCTTTTTTA AGAGAGGAAG 300 GAATTCTGTA AATTCAAGGT ACTGTATCAA GATCCTGAGC CTAATGTCAC CCTTTGACAA 360 GCTCAGTAGA ACTCCAGCTG GAAAAATTTC TAGATAATGC TCTCATGCAG ATTTTTCAAA 420 ACTTAAGTAT GAATCTTGGC ACAAAATGTG CTCGCTCATC CACATAAATC TCATTACTGA 480 GGCAATAAAC CTTGCAATTG CTTGTGCTGT CTGCAACGGC AAGAGCTGCA GTATCCAAAG 540 CCCAGCCTGG CCAAACTCCC CTCACAAATC AGATATTCAA CCTCACAGGA AAAGAGAATC 600 ACTGTTAATT AATAACAACA AAGGATTAGG CCAGTGGTTC TGAACCCGGG ACAACTCTAC 660 TCCCCTCCTC CCCCCAGGGG ACATTTGGCA GTGTCTGGAG ACAGTATTTG GTTGTCGTTG 720 ACTAGGAGGT GCTCCTGGCA TCCAGTGGAT AGATCCCAGG AATGCTGCTG AACATCTTAC 780 AATGCATGGG ACAGTCCCCA CCCCGCCCCA CAGCAAAGAA GTATTAGTCC CCAAATGTCA 840 ATAGGAGTAC GGTTGAGAAA CCCTGGCTCT TCAGACATAT GGAGCCTTAT TAGATCTTCC 900 TGGGCTAAGA GCTTTACAGG AAAGATCTCA TTTAATCCTC ACAGCAATCC TAGGTATAGG 960 GCCTATTATC ATGCCCATTT TACAGAAAAG GAAACTGAGG CTAAGAATCA CATACCATTT 1020 CTAGGCCGGG CACGGTGACT CATGCCTGTA ATCCCAGCAC 1060
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