Tag | Content |
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EnhancerAtlas ID | HS038-01635 |
Organism | Homo sapiens |
Tissue/cell | ESC_neuron |
Coordinate | chr1:204616020-204617040 |
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 | TGCTCAAGGA CACTTGGCAG GTGAGCCCAG CTACAGCCAC CAAAGACAAG ATGAGCCCAG 60 CCATGGGGAA AGAGCAACTG GATTCCAAGC CAGGGTTCCG TCTCAACCCA GAAGCTTTTA 120 CCCACTTCTT GTAGGGATGG CAGAGCCTCC ACGAGTGTGG CTGGCTTGAC TTTTGCTGCA 180 ATAGGCAAGG GGGTGCCCAA GAACTTGGCC TGCAGTGACT GGGATTGCAA GATTCTGATT 240 CCAGGAAAGG AAGCAAGGAG GTTAAAAAAA AAAAAAAAAG GCTAGAAAGT TAAGGAGAAA 300 AGAAGGCCTT AAAGAGACTG GTCTGGCAGG GTTAATAGTT TCTTTCCTTC AATAGAGATT 360 TCATGCCACA TTGAATAAAT AAAATACCAC ACAATTGCAA AAGATGCATT CCACAGTATA 420 TTAGATACCA CCACACTGTT ACCCACATCT GTCAGCTACT ACCATCAGAG TGACTGATGA 480 CTTATCAAAA GCCACTCTGA CATTTCCAAA TGAGATATTT TGATAGAGGT GCCATTCAAC 540 AGGGCCAAAA AAGCAGATAG AACTTGAATG TAAATGAGGA ACATTTGTCA CCTTTGTCTC 600 ACCTATTTAA AGGTTTCTTG TCTGACAACA AGGAAAGGGA GAGAGGGAGT GAGGGGAGAG 660 GAGGTGGAGG ATGGGCAGGT AAGAAGGTAA GAGGGAAGGG GAGAGAGCAC CAACTCCAAA 720 AGAGCCCAAA GGAGAAGGGC TGGTCCCTGA GAGCAGTAGG AAGTGAAAGA GAAGCAAAGC 780 CCAGATGGAC GGCTCTGATT TTTATGCGGA GTCACTCTAT GACTCAGCAG GAAGGAGCAG 840 TATCAAGAAC AAAGACCAGA GCTGTCCAAG GTGGCAGCCC CACATGAGGC CACTGGGTAT 900 TTGCAATGTG GCCAGTCCAA ATGGAGATGT GCTGGACATG TAAATGTACA CCAGCTTTCA 960 AAGATTTAAT ATGAAAAAAG AATGTGAAAC ATCTCATTCA TGAATTTGTT ATTGATTGCA 1020
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