Tag | Content |
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EnhancerAtlas ID | HS145-16218 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr22:46291690-46292940 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr22:46292479-46292497 | GGCAGGAGGGGAGGAAGG | + | 7.16 | EWSR1-FLI1 | MA0149.1 | chr22:46292483-46292501 | GGAGGGGAGGAAGGCAGG | + | 7.36 | ZNF263 | MA0528.1 | chr22:46292470-46292491 | GAGGGAGGAGGCAGGAGGGGA | + | 6.41 | ZNF263 | MA0528.1 | chr22:46292476-46292497 | GGAGGCAGGAGGGGAGGAAGG | + | 6.7 | ZNF263 | MA0528.1 | chr22:46292473-46292494 | GGAGGAGGCAGGAGGGGAGGA | + | 8.45 |
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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 |
GH22I045896 | chr22 | 46292223 | 46292973 |
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Enhancer Sequence | ATGGCTGGGG AGAGGGCTGT GGTCTCAGCA GCACTGAGGT TGGTGGCCCC TGTCCTTGCA 60 GCAGGCCTGG GAAGGACAGG CCTCTGAAGG CCACAGGGAG AAGCCACCCG GTACCAGAGC 120 CAGGCTCTGA CCCCAGCCAT CCTGCCGGCC GCGGTGCTGC CTCCGTGCAT CTTCTCCAGG 180 ATGCTGAGCT CTGTCCCCAG AGCCCAGGGG AGGCTTCCAT GCTGCAGATC TGGCAATGGG 240 AGTGCTGGGA GCAGCGCCTG TGCAGACTCC GGCTGTGGAT GAAGCTTTAT TAGCCCAGGC 300 AGGGAGTGGG GCCACACAGC CGTCAGGGCA GCGTTGGGTG GAGAAAAACG TGACAGCGTG 360 CCCCTTACAG ATGGAGCCAT GGAGGCCAAG GTGCATGGCT CAAGTAGCTG CAGACTGGAG 420 ACAGAGCACT GAGCTAGGGG TCCTGAGCCC CTGTCCTCCA GGGCTCTGCC CTTCACACCG 480 AGAACTGCAT CCTCAGCCAT CAAGGGCCAA GCTGCTCCGG CTGTCCACAG GGGACCCATG 540 GTTGACCAAG GTGGAGGCCC TGGGGATGCA GAACTGGATG CTGGGAAGAG CTGGCTCCTC 600 CTAGCTCTGT TTTACAGAGA TGGGAACTGA GGTCTAGAGA GATGCAGCTG GCTTGCCAGA 660 GACCACAAGG AGGGCAGCTG CTTCCCCAGA TGCCAGGTCC CTGGGGCTGG AGAGGGGCCT 720 CTGGGCAGAG CCCTTCTCAG GAGGGAGCCT CGTGGTGGCT CTTTCTTATG GAGGAGAATA 780 GAGGGAGGAG GCAGGAGGGG AGGAAGGCAG GCCCTGTCTG ACCATGCAGC TTCTTGTAAA 840 AACCTAAGAA AAGCTGCCGG GAAACTCATC CGCAACCGGT TTGGCCAGTT CCTAACATCC 900 TCCCTGAGAA CCTGGGTTCA GGCTCACTGT TGCCGAGCCA TTCTCCCAGG CCTCCTGTGC 960 GCTATGCGCT GGCCGGGCCT TACGGTGGGG AGGGGCCTCC CCCATGGGCT TCGTTCCCAG 1020 GCCTGTAGCA TGAGGACTTG TCTGCAGTCA CCGAGAGCCC CTCTGGTCCT AACACCCTGG 1080 TCACGGCCTG GCACTGAGCC CTGGAGAAAG AGCGTGACGC TGATCCCTCG CTGGCCGCCT 1140 GTCCAGCACC AAGCAGGGAT CTCGCATCCT CCAGCTTTGG TTTTGCCTCA CCCCAGCCCC 1200 TGATGGGGGA AACTTTCTCC CAGTCAAGGG AACGTATGTC CCAAGAGGGG 1250
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