Tag | Content |
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EnhancerAtlas ID | HS048-15064 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr16:89697230-89698050 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr16:89697383-89697401 | GGCAGGAAGGAGGCAAGG | + | 6.62 | Zfx | MA0146.2 | chr16:89698023-89698037 | GAGGCCGAGGCGGG | - | 6.01 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH16I089631 | chr16 | 89697242 | 89700208 |
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Enhancer Sequence | TTCTCTGGGG GTGAGACTCG TGTGCCCTTG GGTTGGGGCT CAGTTTCAGC TTCTGCGACG 60 GTGCCGGGCC CTTGCCCTTT CCTGGCCCCT GCTGCTTTGT GGGGTCTCTC AGGGCCCCCA 120 AAGACTTCAG CGGATGAAGG TCTGCAGGGA CTGGGCAGGA AGGAGGCAAG GCCACACTCC 180 CTGGTCCCGA AGCTCAGAGT GAGGTCTGAG CCTGCGGACG TGGAGGCCCT GCGCCCCAAT 240 CTCACCCTGT GCCTCAGCTT CTCCCAAAAG CAGCAGGTGC GGGTGGCACC CTACAGGCCC 300 TCTCAGCCGG CATCTTTTTG GCTCTCTTCC CACTCCCCCC GGCCTGCCTT CTCCCGGGGG 360 GAGGCCCATG CCACTTGGGC CCTTGCCTGT GCTGCGCTGT GTGCCCACCC GGCCCCCACC 420 CCCGACCTCG CTGGGGCACC TGGGTCACCT GCTTCTGTCC TGACCTCCTC AGGGCGGAGA 480 TCCCCACTGC CCGGGAATCC GACCCTCTTC CCCGCCCCTT CCTGGCCCAG TGCCCCGACA 540 CTGGGTCACC ATGGAGGCCT CCTGCTTCCA GGCACCAGAC TCAGATCAGG GTCCACACTG 600 GCTCCGCGTT GGGGTGGGAG GGTCACTGAG AGTCCGCCCT GTGTCTGGCA TGGTGTCTCC 660 ACCTGGAAAA TGCCTCTGGG CTTTGTTGGG GAAAAACTGT GAAAAAAGCA GGGAAACCCG 720 ATGTCTTGTC GCATAAGAAC TTCAGGGAAC AGTCCAGGCT GGGCAGTTCA CGCCTGTAAT 780 CCCAGCACTT TGGGAGGCCG AGGCGGGCGG ATCACCTGAG 820
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