Tag | Content |
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EnhancerAtlas ID | HS185-00762 |
Organism | Homo sapiens |
Tissue/cell | T98G |
Coordinate | chr1:204616160-204617120 |
Target genes | |
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 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH01I204647 | chr1 | 204616528 | 204617430 |
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Enhancer Sequence | CAGAGCCTCC ACGAGTGTGG CTGGCTTGAC TTTTGCTGCA ATAGGCAAGG GGGTGCCCAA 60 GAACTTGGCC TGCAGTGACT GGGATTGCAA GATTCTGATT CCAGGAAAGG AAGCAAGGAG 120 GTTAAAAAAA AAAAAAAAAG GCTAGAAAGT TAAGGAGAAA AGAAGGCCTT AAAGAGACTG 180 GTCTGGCAGG GTTAATAGTT TCTTTCCTTC AATAGAGATT TCATGCCACA TTGAATAAAT 240 AAAATACCAC ACAATTGCAA AAGATGCATT CCACAGTATA TTAGATACCA CCACACTGTT 300 ACCCACATCT GTCAGCTACT ACCATCAGAG TGACTGATGA CTTATCAAAA GCCACTCTGA 360 CATTTCCAAA TGAGATATTT TGATAGAGGT GCCATTCAAC AGGGCCAAAA AAGCAGATAG 420 AACTTGAATG TAAATGAGGA ACATTTGTCA CCTTTGTCTC ACCTATTTAA AGGTTTCTTG 480 TCTGACAACA AGGAAAGGGA GAGAGGGAGT GAGGGGAGAG GAGGTGGAGG ATGGGCAGGT 540 AAGAAGGTAA GAGGGAAGGG GAGAGAGCAC CAACTCCAAA AGAGCCCAAA GGAGAAGGGC 600 TGGTCCCTGA GAGCAGTAGG AAGTGAAAGA GAAGCAAAGC CCAGATGGAC GGCTCTGATT 660 TTTATGCGGA GTCACTCTAT GACTCAGCAG GAAGGAGCAG TATCAAGAAC AAAGACCAGA 720 GCTGTCCAAG GTGGCAGCCC CACATGAGGC CACTGGGTAT TTGCAATGTG GCCAGTCCAA 780 ATGGAGATGT GCTGGACATG TAAATGTACA CCAGCTTTCA AAGATTTAAT ATGAAAAAAG 840 AATGTGAAAC ATCTCATTCA TGAATTTGTT ATTGATTGCA TTTTGAAATA TTTTTGCTAT 900 ATTGGGTGAA TATGTTATTA ACTTCACCTG TTTCTTTTTG CCTTTTTAAT GCAGCTTGCA 960
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