Tag | Content |
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EnhancerAtlas ID | HS050-14542 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr11:133581100-133582810 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXP1 | MA0481.2 | chr11:133581945-133581957 | AAGTAAACAGTA | + | 6.18 | TCF7L2 | MA0523.1 | chr11:133581914-133581928 | TGACATCAAAGGCA | + | 6.22 |
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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 |
GH11I133712 | chr11 | 133582221 | 133582430 |
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Enhancer Sequence | CTCATCTTTC TCCAAGGCAC TGCTCTCCTC CTAGCACTCC CTACATTCAT CTCGTCTGTT 60 GCCTGTCTCT TCTAGAATGT GTGCTCCATG AAAAAGAGGA GGTCTGTTTT GTCTCCTGCT 120 GTATTGCCTG TGCCTAGGGC AGAGCCTGGC ACATACTAGG TACACAATAA TTTGTGGCTG 180 AATAAGTAAT TTATAGCCAT TATTATATGT CTGGTATCAA TACATCCAGA CTAGAGCTCT 240 TGAATTACAT ACACACACAC ACACACACAC ACACACACAC ACACACACCT CATTTATTGC 300 CCAGTATTCC TCAATCAATG CTAGAAACAT GAGATTCCTC TTCCCCACAG CCCCCACACT 360 CGATCCACCA CAGACCTAGC TACTCTGCCT TCAACACCCT GACTCCAGCT TTCTAATCCA 420 TCCCCCATCC TCCCTGCTCT TAGCACTCCT CCAGTGCAAA CCACTCTCCA AAGGTTGCAG 480 TTGCTTCCAG TGCCCTCCTC AGAACCTCCT ACAGGCTCCC TGGCTCACTG GGCTCTCCTC 540 CCTTTGGCCT CCATCCATTC CTAGGCATGT TCCTCCAGCA TCTGCCGCAG GGGCCAGTCT 600 GCGCTTTCCC AGCTCTCTAC CTGGAAGGCT GTTCCCTCGA TTTCATTTTA ATCTCCAAAC 660 AGCTTCCCTG ACCACTCAGT CTACAGCAGC CCCCACCTAC ACCCTCCCCT CCACTCTTCC 720 CACCACCACT TCTGTTCCCT AGAGCAATTA TCACCCTGCA ATTACCTCAT TTATGTATGT 780 ATATGTTTTC TTTTCTAGGA CCCCACTGAA ATTCTGACAT CAAAGGCAGG AACTTAGCTG 840 GGAATAAGTA AACAGTAGGC CTCCAAATGC ACAGGGAGTG GATGGATGAA AGCCAGTTTA 900 AAAGGGCTGC AGTCTCCAAA GTCTTCAGCT GTCCCTGTGC CCTGGGAGCA GCTGTACAGA 960 GGCAGGAGGA GGATGAAGCA GGAGCTCCAA GAACATCTGG CCGTCAAAAC TAAGGGGTCT 1020 TACTTCCCGC ACTTCTCAGC CCATCCTTGG TTTTCTTCTG TAGCAATTTA TTTGCCTCTA 1080 TTTTGTGGGA GGAAGGAGAG CCTTCTCCAG CAAGAAGCAC CGTCCCAGAC AATATTATTT 1140 GAAAGGGCTT AAGAAGCAAG AAATAACTCA TCCCAAAATA ACCCTTACTT GGCTTCCAGC 1200 TGCTCTGAAC AGCTGGATGC TTTTTCCTAG CCAGATAGCT ACTGTCTCTA TGCTAATAAC 1260 ATAGGGAGAA ACCAAACACA GTGAGATATG CTAAATGGGG TCGCTGTTGT TCATTCCCTT 1320 AGGAGGAGAA ATGCCATTAG CATTCTCCAT GCAGATTTTC AGCAAAAAAG TTTTAAACCC 1380 TGTGCTTAGC ATCCTTGGGT TGGGCACCAT CAAAGAATTA TGAAGCAACC GTCCTCGTAG 1440 AATTTACAAA CTAGCTGTGC TGAGAAAAAA TGGCACATAT CAAACAATTA GCAAACAATA 1500 TGATAGAACA TAATTAAGCA CTAAGCAGTG TCGTTCAGGT TCAGAGAGGA TTGAGGCGAA 1560 GAGTAATTGG GAGAGACTTC TTAGAGGAGT TTCAAGCTCC ATTTGGAAGG ATCTGGAAAG 1620 TTGAAGAAAA GTAAGGCAGT CCAGAGAGGG GAAATATTAA AAGAGTCTTA GAGGCATGAA 1680 GGAACCTGGA CCAATTGTCC TAATTGGAGT 1710
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