Tag | Content |
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EnhancerAtlas ID | HS179-06056 |
Organism | Homo sapiens |
Tissue/cell | SkMC |
Coordinate | chr11:8673450-8674580 |
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) |
EWSR1-FLI1 | MA0149.1 | chr11:8673688-8673706 | CCTACCTTCCTCCCTGCC | - | 7.03 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr11 | 8673800 | 8674012 | chr11 | 8673723 | 8674075 |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I008651 | chr11 | 8673420 | 8674469 |
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Enhancer Sequence | CTGTGCAAGA AAGAAAGATA GCAGAGTCAG GGCAACATGG CTGATTATAA CTAAGGCCTG 60 GACATAAGGC TTTCTAATAC ACAACACCAA GATACATGGC AATACCCATG TGTGCCAAAA 120 TGAACTACAC TTGATGCCAT AGCCTGCATT TAGTATGTGG GTACCCTGAA CATGACCATC 180 CCATTGGGGC CTTCCCTACA GACCATCTGG TCTCCTCACA TTCTTGTCTT TACCTGGTCC 240 TACCTTCCTC CCTGCCCCAT AAACCATGCT ACTACAGGCC CAACGCTGCT TTGGTTCTGA 300 CAATCAGGTG CCTTCTTGCT GCTCCCATTC CTCATTCCAC ATCCCTGAGA GCACAGCTCC 360 CATCACTAGC CAAGATCCAG AGTCAGTTTA GTCTGGGCAC AGTTCCAGGT CATTAAGGTT 420 ACCACATAGC AGGATGACTT GGAAGATCTC GAAGCTAAAG CCTCCAGAAG GCTTTAGTCA 480 GAGAAAGGCA AGGCCTCCCT GCCCGCTCAT CTAGGAGGTA TTTTTCTCTT AGTACAGCAT 540 ATACCAGTCA GTCTGCCTCT GAGGCTCAGA GGTCTTTTGG AGGGCTCTCT CCCCATAGAC 600 CAAGTTAGAT GCATCATATA TATGTATATT TTACCTATGA ACAGCTTGAC CTACAATCTC 660 TCCCCAGAGA AATACATCAG TCTCTAACAT ATTCTTCAGC ATAGTGGGCT TCTGGACTAT 720 AAAAGCAGCA GAAGACTCCC ACCCTGGAGA CCACAGTGAT TCTGCCGGCC CACCGCAAGG 780 GCAGTCAACC TACTAGGAAC AAGAAAATGA GCCTCTGGAG TAGGGCAAGG TACCTGTGTC 840 CAGGGATGAG GGTGATCTGG AAAGGGGTTG GCTATGGCAG TGAATGCAGC AGTACCGCTA 900 CAATCTCCTC TGTCTCATCT CTTCAAAATA CGAAAGAATG ATATGATGGC AGTTGCTCCA 960 GACTTATAGT CAGACAAATG TAAGTCCAAA ATACCAGGCC TACCAGCCAA TGACCTTGGG 1020 CAAAACACTT AATCTCACTT AATTGCCCTG TACCCCAGTT TCTTCATATG TAAAATAGGG 1080 AAAATAAGAG TTGCTGTGCA CATTAAATTA GATAAGACTT CAGAAATCAC 1130
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