Tag | Content |
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EnhancerAtlas ID | HS048-33900 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr7:50682580-50683900 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myog | MA0500.1 | chr7:50683446-50683457 | CTGCAGCTGTT | - | 6.02 | RREB1 | MA0073.1 | chr7:50682762-50682782 | ACCCAAAACACCCACTTCCC | + | 7.61 | Tcf12 | MA0521.1 | chr7:50683446-50683457 | CTGCAGCTGTT | - | 6.62 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_41576 | chr7:50681779-50682767 | LNCaP |
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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 |
GH07I050613 | chr7 | 50681368 | 50684228 |
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Enhancer Sequence | TGACAACACT GGCCAGGTTA AAGTCTCAAG CACAGCAAAG AGCAAATGTG TTCACCTCTG 60 GTAGACAGAG GGCAGTCTCT GCACACTTAC AAGCACTTTC CCCGATGACA CTATACATAT 120 TACATATGAT TATTACGCGA GGTGTAATAA GTGCTAAACT AAAACCAAAT TCACCCAGTC 180 TCACCCAAAA CACCCACTTC CCCAGTTCTC AGACACACAA GGCTGTTGGA ACGTATTTGA 240 TACTTCTGGC AAATCAAAGC CCCATGACCG GATATTCAAG ATAAAAAGCA GGAGAAAATC 300 TATAACCCAA AGGTCAGAGT TAAGAGCACA GGGCCTGTCT GCCTTTGGTT TGTTGTGAGT 360 CCAGAGTCCA ACCGTACTTT GGGTTTTCCC ACTGGTAGCT TGCTTGTCCC ACCCTTCTCC 420 TCCTCAACTC TCCAGCCCAG CTCTGTTTCC TGCTCTACGA AATACCCTCC CAACTTCAGC 480 ACACACGAGG ACAGTGAGCG GGCCACACAG CAGAGCTGGG AGGTCAGGAA GCTACCATGC 540 CCTGTGTCAG TTCAAAGCCC CTCTCTGCAG ACGCCCCTTC TCTCTGGCCC AGGTGTCGGC 600 AGCTGCTGAC TTCCCAGAGC CGGCCCCAAC ACCTTCCCAG AGCCGGTTCC CAGATGCTCA 660 ACACCTGTGC TGGGGTCCCG CCAGCTCCCT TTCACCTCTG CTGGCCAGAG CAAAAGAGAC 720 CACAGCCCTC AGATGGTAAG TGCTCAGCCA GGTATTGGGT GGACAAGGCT CCTGCCACAG 780 GGTATATGTG GACAGCACAA GAAGAGAGCA GACAAGAGTG TACATGGGAG CAAAGGAGCC 840 TCCGGCCTAA GCTCTCTTTT GAGGGCCTGC AGCTGTTTTC CATCTCCCAC CTTCTTCTCA 900 CTGGGGATAC ATGCAAGCCT GCAGTTTATT TCATGAAATA TCTATGATAC ATAAAGTTAC 960 ACTGGCATTA GGGTGGCAAT AGTCTATCAA ACATCTTTAC AGCTAGCTTA AATCCCAACT 1020 TATGAGAACT AGGCCAGTCT CTGAAGTGAT GGGGCAGCCA GGGGTGTCTG CTCCCAACCC 1080 GCAGTGGGGG TGGGGCTAGG CAGGTGGGGT TCTTAGGCCT GTATTATTTA TTACCTAGTT 1140 TCTGAGCGAG ACCAGGAAAC CTGTGACTCC AAGTTCAGCT GCTGCACAAT TAGCTTATTA 1200 AGAAGTTGTC CTGAGCTTGG AGGAGTCTAA GGTGCATTTA AAAATGAAGC CCAGGTTCAC 1260 TCTGAGGACC TGGGGGGAGT GACTGTGGCA GAATTAGGGC TGGTGGTGGT AGCTTTTAAA 1320
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