Tag | Content |
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EnhancerAtlas ID | HS069-06904 |
Organism | Homo sapiens |
Tissue/cell | GM18951 |
Coordinate | chr5:169765560-169766890 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MAFF | MA0495.3 | chr5:169766581-169766596 | CTGCTGAGTCAGCAA | + | 7.63 | MAFF | MA0495.3 | chr5:169766581-169766596 | CTGCTGAGTCAGCAA | - | 7.64 | MAFG | MA0659.1 | chr5:169766578-169766599 | GCTCTGCTGAGTCAGCAAAGA | - | 6.61 | MAFG | MA0659.1 | chr5:169766578-169766599 | GCTCTGCTGAGTCAGCAAAGA | + | 6.82 | MAFK | MA0496.2 | chr5:169766579-169766598 | CTCTGCTGAGTCAGCAAAG | - | 7.13 | MAFK | MA0496.2 | chr5:169766579-169766598 | CTCTGCTGAGTCAGCAAAG | + | 7.48 | SPI1 | MA0080.4 | chr5:169766135-169766149 | AGAAAGAGGAAGTG | + | 6.51 |
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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 |
GH05I170338 | chr5 | 169765521 | 169766170 |
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Enhancer Sequence | ACATGGCTGG GCAGAAGGAA TCCAGCAGAG GGTTGGAGGC CGGAATAGTA TGAAGTGTCC 60 AGAAATAAAT CCTGGTTATC CAGAGAGGGG GATATTTCTT ATGGTGACCT TGGCCCAGTT 120 GAATGCCCTC TGCCTCTCCC CACTCCCATC CCTGTGTCTG GGTCTCTGGT CTCTGTACTT 180 AGCAGAACTT GCTGAGAAGA ACTCTGAACC TGGGGATGGG GGAGCAGGTT GAGGGTGGGA 240 TATAGACCAT CAGGTTCCGA GTGAGGCTTG CAGAGCTTGC AAACTATGAG TAGAAACAAC 300 ACTCATTTTA TAGTCAAATC TAGCCTTTGC TGCCTGTGAC TCCTGAAAAC ATTTCCCAAA 360 ATTCACTGAG ACCTCCCATC ACTGGGAGGG AGAGCTGCCT CTGCCAAGCC CCCTGACCCA 420 CATCCTCTCT GGGGCAGAAG GGAAACCTCA CCTGGCCAGG TGGGCTGATG GTAGAAGTGG 480 GAGCTTGAGC TCCCTCTAGT GAGGCAGTGG GGGCAGCACA GAAAACACCT CCAACCTAGG 540 CACAGGGTGA CCTCTGCAGG ACTTTCTCCC CATCAAGAAA GAGGAAGTGG CATTGAGTGA 600 GTCCTGGTCA AAAATAGTCC ATTTCTGTGG GTCCCAAGGG CAGTCCCGGC TCCCCAGCAG 660 AGATCTTTTG AAATGCTCAC TCTTCTGAGG TCCTTGGCTC TGAACCCAAA ATTCCCCCAT 720 CTGTACACAT GCAGATCTCT GGGGTCTGGG CGCATGTGAT CCCCCGCAGA CCTCCCTGCT 780 GGAGGTAGCC TCCTTCCCAT CCTTTCTCTG CCAGACCAAG CACACACTCT GCTCCCCTTG 840 CTGGGCCTTG GGTTGGGTTT GTCCCAGCTC CTGCCCTGGT TGGGGGTGAG GGGTAGGTCA 900 TGACAGAGAT GGAGCCCCAT TTTCAGACTT AGCTTAGCCT CCTGGAAATC ACCCTAAAGT 960 ATTTTTGGAG CTATTTAGCA TCCTAAAGAT CAGAAAACTA TTGCAACCAG ATGCTTGAGC 1020 TCTGCTGAGT CAGCAAAGAT GCCCACAGCA GTGGGGAGCA GACCCTGGCC TGTGTCACTG 1080 TGAGTGAGCA GTGTGACTTC TCAGGGCTGC AGTCTCCTTG TCGGAAAATG GAAACTAAAA 1140 TTGCTGGGAT TAAAAGGGAG GAAAATATGG GAAAGCACTT TGGACAGTAT AGTGTGCAAG 1200 TTGATGTTAG TATCTATTAT TTTTAAAATC CGGAAGTCAG CTAAGATGCC TTATCCTATA 1260 AAACTCAAGT GGATTTTGCC AGAATGTCCT CACACCAAAT AGTGGACCCC TTCTTTTGCT 1320 GATTTATCTG 1330
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