| Tag | Content |
|---|
EnhancerAtlas ID | HS050-01955 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr1:41987090-41987990 | SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr1:41987728-41987746 | GACAGGAAGGCAGGAGGG | + | 6.28 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AGGAGTCAGG ATCGGAGGTG ACTTTGCGGG TCCAGGAGTG GACACTGGAT GGGCAGCCCT 60
GAGTGCTGTC CGGGTCCCTC TGTGACTTCC CCTCTCCAGG CCTGTCTCCT CCTCTGTGAA 120
AGGGGAAGGT GGGGCACACG GCTGCAGGCA CAGCCTGAAC ACCACTTCCC TGTTGAGGGC 180
CAGGGCCTCA GCTTGTCAGG CAGAGCCACA GCTTCTCACA GTCATCCCAG ACCCCACCAA 240
AGCCTGACAG GCCTGGAATG AAGAGGAAAG GCAAGTGAGA GGTAAAGTGA TGGGTGTCGG 300
GAAGAGGCGG AACCTCCGAT AAAAGGGCAT CCACCAACAA CCCTGCCTGC CTCATTTGGC 360
TTTGATCAAC CGCTCTGTCC CTGCCCCTGC CGCTGGCAGA CCTGAGGCCA TCTCTGTCCC 420
CTGAGGCGAT CGGTGCAAGG GCCTGGACAT GGCACAGCCA TCCGCTGGCC TCTGGGAACC 480
ATCTGAGAAG AGGAAATGGG ACCCCCAGCC ACCACAGGGC CACCCACAGG CCTCCCCAGC 540
CCCACCTACT GACGCATTCC TTAGCCAGTT TCCAGAGGCC TGAGCTGCTG CCACGACGTC 600
TGACACAAGA GACGAGACAC ACACGGCAGA CAGAGACAGA CAGGAAGGCA GGAGGGGCTC 660
CCCAGGCCCT GGTGTAGCCG GGTGGTAGGG TCGGGAGGGC TGCCTGGGGC AGGCCTGGAG 720
GTGGCCCAAT GGGGAGGCAC ACAGCCCCGG AGACAAGGGG CCTGTGTTGT CTGAGCTGAT 780
GGCTGACGGG GCCCAGCACT CCACAAAGAC ACCTGGCCCC AGAAACAGAC AGGAGCTCCA 840
GCGCCCTGCT CTCCCTTCAC CCCCATACTG CAGAGAGAGT TAACAGGGAG ACTTCCCTGC 900
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