Tag | Content |
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EnhancerAtlas ID | HS092-32094 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr5:122205700-122206820 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXP1 | MA0481.2 | chr5:122206053-122206065 | ATGTAAACAGAG | + | 6.32 | FOXP2 | MA0593.1 | chr5:122206053-122206064 | ATGTAAACAGA | + | 6.02 |
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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 |
GH05I122870 | chr5 | 122205988 | 122206690 |
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Enhancer Sequence | CTTTTAGGGA AACTTTAATC AACACCTGAT TTGCCCTTTT GGAGAATGTC TTCACCCTGA 60 ATGCTGCTTC TTTTGGATTT AAATATTGTT GAGTAAAAAG CATTTTGCTT GTAGTATAGA 120 ATGTTTTTCA TCTAGGCCTC ATGTGAGAAT TTTCATATAA TTCAGAACTT TAGAATGGAG 180 ATGTACAAAG CTTTTTAGTC TCTATCAACC TAAAGATCTT TGTTGTTATT CAAAATGTGT 240 GCCTTGGAAA TTTAGGATAA TCTTTTGAGC TTTGCATCCC GAGGAGCTGT AAGTAATCAA 300 AAAGCAGCAG GAAGCTCCGC TGCTTCAAAA CTTTGTATGA TGAACTTCTA CAGATGTAAA 360 CAGAGCTGCT CTCCAGAACA GAAAGACCTC AACCCTGCCC ACATCTAGTG AATAGCAGTG 420 GGCCTGAGAT GTCAGCTTAG TTTCAGCCAA TGACCCTTAG TTTCAGTGTT GTTCCTTAGC 480 CTGCAGCTTT GTACCTAAGT TTAGTGTATT CAGAACAGCA TATTGTCCAT GGCTGCAAAA 540 GTAGTGACAG TTAAAAATGC TAATAAGAGA GAAACGGAAG TGGAGATAAT AAAATGGAAA 600 GTGGTGGAAG AATGACAAAC GCGTGTGCAT GTGGAATGAA TCATCCAATC ATAGGAATGA 660 TTCTTTAGGA CAGAGGGGAG ACTCATGCAG CATTTCTTGT AAGCGGGCAT GCACGTGTGC 720 AGGGAGTTGG GGGAAGTGCC TGAGACATGG AAAAACTTCA GGTGTTAGCA CCACTTCAGG 780 TGCCTGACCC TAAGGGAGAA GGCAGGGAGT TTGAGAAAAA GGCTGTTGAT GTGGTGGTGC 840 TGCTGGTGGA TGGCACATTG GAACACCAGC AAAGGAGGGT TTGGGCTTCT GGTGCACGTC 900 GTTGTCTGCT AAAACCATGG TGCTCATCCC TTGCTGCACA CTAGCATCAC CTGGAGAGCT 960 TTACAAACTA CTGATGCCTG GGGCCCACCC TCAGAGAATC TGATGGTCTT GGGGTATGGA 1020 TTGAGCATCA GAATTTTCTA AAGGTCCCTG GGTGATTGTT ATGAACAGTG GAAGGTGAGA 1080 ACTACTGCAC TGAAGATGTC TCCAGGATGC TTTTGGAGTT 1120
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