Tag | Content |
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EnhancerAtlas ID | HS182-09871 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr17:72726090-72727230 |
Target genes | Number: 15 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ETV6 | MA0645.1 | chr17:72726589-72726599 | AGCGGAAGTG | + | 6.02 | SPIB | MA0081.2 | chr17:72726587-72726599 | AAAGCGGAAGTG | + | 6.92 |
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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 |
GH17I074730 | chr17 | 72726557 | 72727530 |
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Enhancer Sequence | ACAGTTCCGT GTTTAGTCCT CGGTAAAATG GTAAAAGGGC AGCTCGGGTT AAGGAAGCCC 60 AGTGCCCTCG GCTTTTTCTG CCCGCAGCCC CTCTGCGAGA CAAGGGATCC CTCCTTTACC 120 ACACATCCCA TCTCCCCGCG TTGTCCCGTG CCTGCGGCTG CAGCTGCCCT TGAATTCCTG 180 GGAAGACCTT GGGAGAGGGT TCCACTCCTC TCTCGGGCTG TGGCAGGAAG AGCAGGGCCT 240 TCCCTTGGGA CTCCAGAATC CTAGCATCTC AAGATGGGGA AGAGCAAACA TCTCTTCTTG 300 GACAACGCGG ATGTTTGGGA ACCTCTGAGA CCAGAGCACA GGGCCTGTGA GATCACGCTC 360 AGGGTCAGGA CGCAGCAGTG CCACACTGAT GGGAAGAGAG AGAGGAAAAC TCAGAAAAAT 420 GGGCTTGCCC ACTGGGTCAC AGCCAGGAAG GCAGGGGTTC AGAATGAACA TGGCTTCTGC 480 ATGACCTTCC AGGAGGCAAA GCGGAAGTGA GTGCCTGGTT CGGGTGTGTT CTGGGGCCTA 540 GAATCGGCCC TGAAACACCA GTTCCCAGGG CTCTCCCCAG ACTGGGACCG GCTGGGCTCT 600 GGTAGTGCTG AATAGGGAAG GGCTGAGACC CAGGAGGCCA AGGCTACCTG GCAATCCCTG 660 AGGTCTGGGA CCAGGCTGCC ATGAAGCAAA CCAGGATGAC CTGGTGCCAG GCGTCACCCA 720 CCCCAGCCCA GGCCCAGTCT GCTCTCAGCA GCCAGGGCAC ACCCTGCCCT CAGGGTCACA 780 CCCGCATCTC CTCACCCACC CTTCTGCCTG TCTGGTGAGG AAGGAAGAGA GTGGGGTGGA 840 TGTGGCTGTG GACATGCAAA GTCTGACTCA CGTTCCACAG ACCACAGAGG TGAGATCTCC 900 AAATTTTGCC GCTAGCTTGG CAAGAAAATT GAGGCCGATT TCCTGTGAAG GAAAAAGAAA 960 GTGTGTGGTC AAACTGTTTG TCTAGCCTGA GATGAGACAC ACTGGGCTTT CCCACTGACC 1020 TCAGGGTGGG CCTCCTAGAG CCTGGGCTGC CTGCTTGGTA CCAGCCAGCA CCCGATGTTC 1080 TGGTGCATCT CAGGACAAAC CTGTTGCCTG CTTACGCTGA GTGAGGACCT GAGCCCCTGG 1140
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