Tag | Content |
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EnhancerAtlas ID | HS093-28050 |
Organism | Homo sapiens |
Tissue/cell | HL-60 |
Coordinate | chr7:28122770-28123920 |
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 | chr7:28123775-28123793 | GGGAGGGTGGAAGGAAGA | + | 6.08 |
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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 |
GH07I028082 | chr7 | 28121986 | 28124618 |
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Enhancer Sequence | CAATCCTAGA TCAAGCGCCC CTTCCACATG CTCTCTTGGG GTTCACATCT CTCAGTTTAG 60 CCCTTGTGCC TCAAGTGTAA GTTCCTGTAA CGTCTCAGTA TCCCTGCCCC ACTCGTGCAT 120 ATACCCTAAG GCTGTCTCAC TCATATCACA ACCCCAGAAT CTGCACAAGG CCTACCACAT 180 GACAGCCACT CAACGGATAT TTACTGCATA AACTCATGAT TATGAATATT TTAGTACCTG 240 ACCTATGAGT TATTGATACG TAATGGGAGT ACCATGGGTT GCAGAATAAC ACAGACCTTG 300 TTTCCCATCC CAGCTCCACA GCTCACATGC TATGTGAACT CAGAAAATGT ATGGAAACTT 360 TTTAAGGCTG TTTGCAAAGC TGTAAGAGCA CGACCAACCA CTTACTTCAC AGGGTTGCCG 420 TGAAGACTAA AATACACACA GCATATGAAG TGCCAAGAGT GCTGTATTAT TTTATATTTT 480 TCAAAATGCA GTGCTACAAA CTTCTTTATC ACTATGTCAA TTAATGCTAC TGCTGCCTTA 540 ACCCACAGGC CATCAGATAC ATTTTTAAAG TTCTTTATGT GAGCATTATT CAAGGAAAAG 600 CCTTGTCCGC TGACCCAGCC AGTAAAAACA TTGGGCCCTG ACATTGGGTA AGAAATGTTG 660 CTTACAACAT TGTAACATTG TTGCAACATT GTCTTACCCA ATGCCAGGGC CCAGTGCTAT 720 TACTCAAGCA GGCTGGAACA TCCAACAATT TCTGCCAGCC TAAGAATTAT TGGTATTGCT 780 TTTACATGTT ACATTTTATG ACAACAAGTC TAACAATATA AAGCAAATAG TGAAATAGCT 840 TGTTTCTTTC CAGGATTATC GAATGAGGGC AGAAGATGTC ATGGGTATAT TTTGATAAAT 900 ATTTCAGGCA TTACAAACAA TACTGAAATA TATGCCAGTC TTGTAACCAT CACACTGCAA 960 CATTTTCTGC TGCCTTCTGA AGACTGTGGA AAAGCCCCCT TGCAAGGGAG GGTGGAAGGA 1020 AGAGAGGGAG TTTCTCAGAA AGAGAAGAGA AAAACCTAAC ACTTGCCCAG TATCATTGTG 1080 GGTTTAACAA TTTTGCTTTA CTGATTTTAT GGCACAATCT AGTCTCCCCA TATCCCCAAA 1140 ACAAAAACAA 1150
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