Tag | Content |
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EnhancerAtlas ID | HS134-04517 |
Organism | Homo sapiens |
Tissue/cell | Mesendoderm |
Coordinate | chr1:204616000-204617030 |
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 | CAAATCCCAC CTCCACCACT TGCTCAAGGA CACTTGGCAG GTGAGCCCAG CTACAGCCAC 60 CAAAGACAAG ATGAGCCCAG CCATGGGGAA AGAGCAACTG GATTCCAAGC CAGGGTTCCG 120 TCTCAACCCA GAAGCTTTTA CCCACTTCTT GTAGGGATGG CAGAGCCTCC ACGAGTGTGG 180 CTGGCTTGAC TTTTGCTGCA ATAGGCAAGG GGGTGCCCAA GAACTTGGCC TGCAGTGACT 240 GGGATTGCAA GATTCTGATT CCAGGAAAGG AAGCAAGGAG GTTAAAAAAA AAAAAAAAAG 300 GCTAGAAAGT TAAGGAGAAA AGAAGGCCTT AAAGAGACTG GTCTGGCAGG GTTAATAGTT 360 TCTTTCCTTC AATAGAGATT TCATGCCACA TTGAATAAAT AAAATACCAC ACAATTGCAA 420 AAGATGCATT CCACAGTATA TTAGATACCA CCACACTGTT ACCCACATCT GTCAGCTACT 480 ACCATCAGAG TGACTGATGA CTTATCAAAA GCCACTCTGA CATTTCCAAA TGAGATATTT 540 TGATAGAGGT GCCATTCAAC AGGGCCAAAA AAGCAGATAG AACTTGAATG TAAATGAGGA 600 ACATTTGTCA CCTTTGTCTC ACCTATTTAA AGGTTTCTTG TCTGACAACA AGGAAAGGGA 660 GAGAGGGAGT GAGGGGAGAG GAGGTGGAGG ATGGGCAGGT AAGAAGGTAA GAGGGAAGGG 720 GAGAGAGCAC CAACTCCAAA AGAGCCCAAA GGAGAAGGGC TGGTCCCTGA GAGCAGTAGG 780 AAGTGAAAGA GAAGCAAAGC CCAGATGGAC GGCTCTGATT TTTATGCGGA GTCACTCTAT 840 GACTCAGCAG GAAGGAGCAG TATCAAGAAC AAAGACCAGA GCTGTCCAAG GTGGCAGCCC 900 CACATGAGGC CACTGGGTAT TTGCAATGTG GCCAGTCCAA ATGGAGATGT GCTGGACATG 960 TAAATGTACA CCAGCTTTCA AAGATTTAAT ATGAAAAAAG AATGTGAAAC ATCTCATTCA 1020 TGAATTTGTT 1030
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