Tag | Content |
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EnhancerAtlas ID | HS051-22718 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr5:177757190-177758870 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZEB1 | MA0103.3 | chr5:177757816-177757827 | GGGCAGGTGGG | - | 6.14 | Zfx | MA0146.2 | chr5:177757416-177757430 | CAGGCCGAGGCGGG | - | 6.62 |
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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 |
GH05I178330 | chr5 | 177757494 | 177759841 |
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Enhancer Sequence | GGGCCTAGGG TCTCCTGCCC ATTTATGAAG GCTCAACTCA CACACGCACT GTATTCTGTC 60 GGCTTTGACC TCTTTCAGTT TATTTGGTGC TCAGTCCTCA CAGCAACCCT GTGTGGTGTT 120 ACTCCCTCCT GACTGGGTCA AGCCGTCTGA AGCCTCCCTC TGCACACGGG TGCAGATCGA 180 GCTATGGCTG AGCGCTGTGG CCCATGCCTG TAATCCCAGT AGTTCACAGG CCGAGGCGGG 240 AGGATGACTT GAGGCCAGGA GCTCAAGACC AACTTGGGCA ACATGGTGAG ACCTCGTCTC 300 TACAAAAAAA TACTATATAT GTACATATAT GGTGTGCACC TGTAGTCTCA GCTACTTTGG 360 AGGCTGAGGC AGAAGGATAG CTGGAGCTGA GGAGTTTGAG GTTGCAGTGA GCCGAGATTG 420 CACCACTGCC CTCCAGCCTG GGTGACAGAG TGAGACCCTC TCTCAAGAAA AAAAAAAAAA 480 AAGATCCAGC CACCTCACCT TGGCCTGTGT GGCCCTGTCT GATCTGTCCC TTGACACGTC 540 TCTGTTCTCA TTTCAGGTCC CTCTACCCAG TGAACCACTA GGACCTCCTC TCTGCTCTTT 600 CACCCCAGCT GCACAATCCT CTTTCAGGGC AGGTGGGCTC TGTGCCTGGG AAGCCCTGCC 660 CACTCCCCAG CCTGGCTACT TCTTGTCACT CAGGTCTCAG CTCAGTGTCA CTTCATCAAA 720 GAGGCACCCA CTGGCAGTCC TACTGAACAA GCTCCGCCTT CACTCTGTCA CATCCTGTCC 780 TGGCTCATTG CATGTTTCCA TTCTGCTAGA ATGCAGACTT CTCAGCCGGA TAAACCTCGT 840 CTCTCTTATT TCCCAGTGCC TGGCATACAG TAGGAGCTTC ATAAGTATTG GCTGAATAAG 900 TGAAATGAGA ACACGAATGC CCAGTACAAA AGGAGTGACT GGCCCCAAGT TGCAAGCTGG 960 CAGAGGCACT GCCTCCGCTG TCATGCTATG TTCCCTTCTG GGGTACTGGC TTGGGCGGCT 1020 TGTGGGTGGC TCTGTGTCAA AGGAACCTCC TGGAAGGCAG AAATGACCCT TCTGGGTATA 1080 TCTGGCAGAG GCAGTTGCAG CGCCTACAAA TCAGAGGAAA GTGAGGTCAT GGAAGGTGGA 1140 GGCTTTGAGG CCAAACACAC CTGGGTGGGT CCCAGCTCTC CAGTCACCTG CTGCATGGCC 1200 CTGGGCAAGC CACCTACACT CCCTGAGGCT CAGTTTCCCC ATCTGTAAAC TGGGCATAAC 1260 ATGGCACTTG TCTTCTGGAT TGTTGTGAGG CTCATATGAT GCCCTGCATA GCAGGCACCC 1320 GGCCAGGTGC CTCAGAGCCC TGTAAATGGT CCCCAAGGAA TCCGCGGCCC TCGGGGCAGG 1380 GTGCGGAGCA GGGAGGGCGA GGCTCTGAGG ACAGAGGCAG CCACCGACAG GAGGGTGGGG 1440 CAGGAGTAAA CACCATAGGG CGCCTGAGTT TAGACACATG CGCCTGGCTT CTGGGTTACA 1500 GGCAGGGCTG GGCCATGTGC AGAGTTTTTC ATCTTTTAAT CCCAGCTGTT ATCAGCTGCT 1560 GGGAAATAGC TGAGCCCAGT CTCCTAGCTG GCACAGGCTT CCTCTGAATT CCACAAAGAG 1620 AACAAAGAGT TCCGAAATAG TGACACAGCT GTCCTGACCG GCAGCCCGGG CAGTCAGCCG 1680
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