Tag | Content |
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EnhancerAtlas ID | HS045-06312 |
Organism | Homo sapiens |
Tissue/cell | Fetal_lung |
Coordinate | chr1:246957420-246958440 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXP1 | MA0481.2 | chr1:246958047-246958059 | CAGTAAACAGAA | + | 6.02 | ZNF263 | MA0528.1 | chr1:246957425-246957446 | AGAGCAGGGGCAGGGGGAGGG | + | 6.61 |
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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 |
GH01I246794 | chr1 | 246957671 | 246958925 |
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Enhancer Sequence | AGGGGAGAGC AGGGGCAGGG GGAGGGCAGG GTTGGGGCAG GGGAAGGCAG GAGGGTGGGG 60 TGGGGAGAGG GCAGGGCGGG GGCAGGGGGC CGGCTGAGTA CCAGCTTGAA TGAAGTACTT 120 GAGCACCCTG GTGAGCTGAG GGTCCTCGCT GAGGTTAAGA AGGTGAGGGA AGGTCATCAT 180 CTGCCGCTCC TGCAGGAGAA GTGGAGAGGG TTGGGTGTCA CCAGTCCGCA CCAGCCCACT 240 GGGGAGAGCA ACACTTCTTT CCCGTCTCTG TGCACCTTGT CAACCCTCCT GGGGAGGGAG 300 GAAAGCTGAG AGGGGCTGGG GCATTGCTGA TGGTGGGGTG GAGTCTCAGG CAGGCCAGCC 360 GTCAGGAGTC TGAGTACATC TGGACTGGAC AGTTCCAAGG AGCTGTCTCC CGGCTGCCCT 420 CCCCAGCTGT CTGCATGCCC CGCTCTGGTC CCCTGCCTGG GCAGCCCCTC CCCATGTCTC 480 CATGCAGCCT CTCATTCTCC CGAAGTGCTG CTGGCTGGCT GAGAATCAGA TGTTGATGGC 540 AAAAAGTGGG GTATGGCACG AACCCTCGCC TGGCAACCTG AACATGTCAT TCGTCCACAC 600 AAGGATTGTT GTGGCGTAGG GATTTGACAG TAAACAGAAC GGGGATGATT ATGCAGCCAC 660 GAGGAAGACT TTTACAGCTT GAAATCCTCT CTGACAAAGA GTAAAGAGGG CAAAAACCCT 720 TCCAATTTTT ACTGTATATG CAGAACCCAA AATCCCGTAT TCCTCCATGT GACCTTACTT 780 GACCCTTGAA GCTGAGAGTC CCAGCCACCA CTTACACAGA ACGTGACTCA GTACAGCCCT 840 AACTGTCTGG TTTCCTGATG CCACAGACCC CACCCTGCTC CACCCCCCAG GCCCTGAGGC 900 CGTAGTTAGG CAGTATGAGG TTCCGGAATC CCCAGCTCCA GTCCCCTAGT ACTCCAGGTC 960 TGATCCTCAA CTTTGGGATT TTCCCAGGGC CTCGTGGCCA CGGGGAGTGG GGTGGGGTGG 1020
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