Tag | Content |
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EnhancerAtlas ID | HS176-42795 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr9:129390080-129391220 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF2 | MA0051.1 | chr9:129390859-129390877 | TAACCGCTTTCATTTTCC | - | 6.44 | MYCN | MA0104.4 | chr9:129390328-129390340 | GGCCACGTGGCT | + | 6.37 | MYCN | MA0104.4 | chr9:129390328-129390340 | GGCCACGTGGCT | - | 6.37 |
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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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Enhancer Sequence | TTGTCCTGTT GTAGCAGAGC AGAGGCGGAA ATCCCAAGCT GCACGCTACC AGGCTTGGGG 60 GCTGTGTGGC AACTCCACAG TCCTTTTGAG AACCCTCTCC CAGACTCTGG CTTTAACACT 120 GGCCTACTCT GTCTTCCCTG GGCCCAGGTC TCAGGGATGG GAAGGTTCTT CAATCCCAGC 180 TCTTTAAGAA GGGGTGACAG GTGGACCTGG ACAATGAAAT GATTTTGAGA GTTTTCTGGA 240 TAACACGGGG CCACGTGGCT TGGGAATGCG GTCTACTAAA CTGGGACCTT GGGGGACAAA 300 AGCCAGGTGA GGACAGTGCC ACATCCCACC ATCTTTCTTG TCTCTGACTC CCGCATACCC 360 TGGGCTTGGC CCTTCCTGTC TATAGTGGGT CATGGGGAGG CCAGAGGCCT GGCTGGGGAC 420 TCAGAGGGCC AGTGGGCTGC TAGGACCTCT CAAGACTCCA TCTCCCAGGG TCCCTGCCTC 480 AGGGGAGCAG CCGGCTGGGT CATCTGTGCA CAGAAGACAC ATCTGTCCTC CACATGTTGC 540 AGGCCGAGCA GAGGACATGT GGTTTGGGTC GTGTTATCTT AATCATATTT ATTAGCCAAT 600 CCTGGGGGAA AAAAGAGTTT GATATTGTTA TGATTCGGAA AAGGTCCCCA AATCTACAAG 660 GCGACAGATC AGGAGAGGCC GCCAGCAACA GCCAGGTCTC AGCTGGGTTC AGGACATGGC 720 TTTGGAAGTT CTTTGGGTTG TCTTAGAGCG ATGGAATCTC TACGCTGCGA AACAACACTT 780 AACCGCTTTC ATTTTCCCAG AGATCTGAAG CGAAATTAAT TACCCCGCCT TGACTGATAG 840 TTGTTCTGTT GGAGTATGGT TCTAATCCTT ATTAACATTC TCTAAAGTCA GGCATGAAAT 900 ATGACTTTTA TACCACACTC TTTGGCATAT GTTTTTCTTT TCCAGGAGAT TTTTCAGGCT 960 ATCTCTAAGC CTCACTGCTG TTCATTATTT TTGCCATAGG TCTAAAGTTG CCATCCCCAA 1020 AGCTAGTCCC GCACAGAGCA CAGCCAAGCG GGGAGGGGGG TGTGGGAGGA ATGACACATC 1080 TCTGCTTGCG ACGCAAATTG CTTCTGATTA TTGAGCTTTG AATATTTTTC TCCATCGTGT 1140
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