Tag | Content |
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EnhancerAtlas ID | HS098-04689 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr1:204616070-204617060 |
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 | chr1:204616264-204616282 | GAAAGGAAGCAAGGAGGT | + | 6.37 | NFE2L1 | MA0089.2 | chr1:204616836-204616851 | CTATGACTCAGCAGG | + | 6.6 | Nfe2l2 | MA0150.2 | chr1:204616834-204616849 | CTCTATGACTCAGCA | + | 6.84 |
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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 |
GH01I204647 | chr1 | 204616528 | 204617430 |
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Enhancer Sequence | ATGAGCCCAG CCATGGGGAA AGAGCAACTG GATTCCAAGC CAGGGTTCCG TCTCAACCCA 60 GAAGCTTTTA CCCACTTCTT GTAGGGATGG CAGAGCCTCC ACGAGTGTGG CTGGCTTGAC 120 TTTTGCTGCA ATAGGCAAGG GGGTGCCCAA GAACTTGGCC TGCAGTGACT GGGATTGCAA 180 GATTCTGATT CCAGGAAAGG AAGCAAGGAG GTTAAAAAAA AAAAAAAAAG GCTAGAAAGT 240 TAAGGAGAAA AGAAGGCCTT AAAGAGACTG GTCTGGCAGG GTTAATAGTT TCTTTCCTTC 300 AATAGAGATT TCATGCCACA TTGAATAAAT AAAATACCAC ACAATTGCAA AAGATGCATT 360 CCACAGTATA TTAGATACCA CCACACTGTT ACCCACATCT GTCAGCTACT ACCATCAGAG 420 TGACTGATGA CTTATCAAAA GCCACTCTGA CATTTCCAAA TGAGATATTT TGATAGAGGT 480 GCCATTCAAC AGGGCCAAAA AAGCAGATAG AACTTGAATG TAAATGAGGA ACATTTGTCA 540 CCTTTGTCTC ACCTATTTAA AGGTTTCTTG TCTGACAACA AGGAAAGGGA GAGAGGGAGT 600 GAGGGGAGAG GAGGTGGAGG ATGGGCAGGT AAGAAGGTAA GAGGGAAGGG GAGAGAGCAC 660 CAACTCCAAA AGAGCCCAAA GGAGAAGGGC TGGTCCCTGA GAGCAGTAGG AAGTGAAAGA 720 GAAGCAAAGC CCAGATGGAC GGCTCTGATT TTTATGCGGA GTCACTCTAT GACTCAGCAG 780 GAAGGAGCAG TATCAAGAAC AAAGACCAGA GCTGTCCAAG GTGGCAGCCC CACATGAGGC 840 CACTGGGTAT TTGCAATGTG GCCAGTCCAA ATGGAGATGT GCTGGACATG TAAATGTACA 900 CCAGCTTTCA AAGATTTAAT ATGAAAAAAG AATGTGAAAC ATCTCATTCA TGAATTTGTT 960 ATTGATTGCA TTTTGAAATA TTTTTGCTAT 990
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