| Tag | Content |
|---|
EnhancerAtlas ID | HS026-01000 | Organism | Homo sapiens | Tissue/cell | CNCC | Coordinate | chr1:41987190-41988040 | 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 | CCTGTCTCCT CCTCTGTGAA AGGGGAAGGT GGGGCACACG GCTGCAGGCA CAGCCTGAAC 60
ACCACTTCCC TGTTGAGGGC CAGGGCCTCA GCTTGTCAGG CAGAGCCACA GCTTCTCACA 120
GTCATCCCAG ACCCCACCAA AGCCTGACAG GCCTGGAATG AAGAGGAAAG GCAAGTGAGA 180
GGTAAAGTGA TGGGTGTCGG GAAGAGGCGG AACCTCCGAT AAAAGGGCAT CCACCAACAA 240
CCCTGCCTGC CTCATTTGGC TTTGATCAAC CGCTCTGTCC CTGCCCCTGC CGCTGGCAGA 300
CCTGAGGCCA TCTCTGTCCC CTGAGGCGAT CGGTGCAAGG GCCTGGACAT GGCACAGCCA 360
TCCGCTGGCC TCTGGGAACC ATCTGAGAAG AGGAAATGGG ACCCCCAGCC ACCACAGGGC 420
CACCCACAGG CCTCCCCAGC CCCACCTACT GACGCATTCC TTAGCCAGTT TCCAGAGGCC 480
TGAGCTGCTG CCACGACGTC TGACACAAGA GACGAGACAC ACACGGCAGA CAGAGACAGA 540
CAGGAAGGCA GGAGGGGCTC CCCAGGCCCT GGTGTAGCCG GGTGGTAGGG TCGGGAGGGC 600
TGCCTGGGGC AGGCCTGGAG GTGGCCCAAT GGGGAGGCAC ACAGCCCCGG AGACAAGGGG 660
CCTGTGTTGT CTGAGCTGAT GGCTGACGGG GCCCAGCACT CCACAAAGAC ACCTGGCCCC 720
AGAAACAGAC AGGAGCTCCA GCGCCCTGCT CTCCCTTCAC CCCCATACTG CAGAGAGAGT 780
TAACAGGGAG ACTTCCCTGC TTCCATTGCC ACCATCCCAA CCTGGCCTTC CCTCTATTAG 840
TCAAACAGTT 850
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