Tag | Content |
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EnhancerAtlas ID | HS048-07955 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr11:125841950-125842980 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
BCL6B | MA0731.1 | chr11:125841983-125842000 | TTCTTTCTAGGCATTCA | + | 7.04 | Esrra | MA0592.2 | chr11:125842359-125842370 | TTCAAGGTCAT | + | 6.62 | Esrrg | MA0643.1 | chr11:125842360-125842370 | TCAAGGTCAT | + | 6.02 | Zfx | MA0146.2 | chr11:125842080-125842094 | GAGGCCGAGGCGGG | - | 6.01 |
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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 |
GH11I125972 | chr11 | 125842123 | 125842790 |
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Enhancer Sequence | AACTGGCTCT CTGCAAAGCT GCCTTAAATA TGCTTCTTTC TAGGCATTCA TAGTGAGCTT 60 TACATATTAC TCTTAAAAAC TGCAAAGGGG TCAGGCGCGG TAGCTCGCGC CTGTAATCTC 120 AGAACATTGG GAGGCCGAGG CGGGCAGATC ACATGAGGCC AGGAGTGCGA GACCAGCCTA 180 GCCAACATGG CAAAACTCCG TCTCTACTAA AAATACAAAA AAATTAGCCA GCCATGGTGC 240 CACACGCCTG TAATTCCAGC TACTAAGGAG GCTGAGGCAT GAGAATCGCT TGAACCCAGG 300 AAGCGGCGTT GCAGTGAGCC AAGACTACAC CACTGCACTC CAGCCTGGGT ACTGGAGTGA 360 GACTCTGTCT CAAAAAAAAC AAAAGAAAAT CAAAAGAAAC TAAAAAGGAT TCAAGGTCAT 420 GGAACCCAGT GAGGCAAGCG GTCATTTACA GCATGTCACA AGAGCCCCAG AATCAACTAC 480 AACTTCCCCA CAGATCTATA CAGTGCACCC TCCCCTCACC TGCTCTCAAC TTTTCACATC 540 ATACTCTCAT TTACATAATA GAGGCAACGT TTTCCCTCCA GATGGTTATT ACTAAAATAG 600 ATGGGTGATA AAAGGGGTCA AGGGTTGGCA ATGTTTCTTA AAAGCTCACT CCAAGAAATA 660 TGCTTAAGTT TACAACTGAG AAGGCAGAGA AAAAAGAACC TGGAGTGGCA GGGCACAGAG 720 CAGGTAAGAG TCCGTACGGA AAAGGCCCCA TGCAAGACTT CTCCAGTTCT CAGTATCTGT 780 GGAATAAAGA AGGCGAATTG CAGAGGCACC ACCAGATCTC AGAGGACAAC TCTCCAGAAG 840 TATACTGTGG GGCAGCTCCT CTTCATCTCC TGCAGTGTTC TCTGCCTCAG TGACTGCGCC 900 CAGACACCTA GACATCATCT TCAACTGCTT CCTCCACTGG CCTCTTCAAC CAATTACTTG 960 GTCTTTTTTT TTTTTTTTTT TTTTTTTAAA TCCCTCAGAC TCATTCAGAC TCATCTCCTT 1020 CTAAATCCTA 1030
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