Tag | Content |
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EnhancerAtlas ID | HS095-31644 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr9:124941230-124942560 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxa2 | MA0047.2 | chr9:124942211-124942223 | CCAGAGTAAACA | - | 6.11 | STAT1 | MA0137.3 | chr9:124941317-124941328 | TTTCCTGGAAA | - | 6.62 |
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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 |
GH09I122178 | chr9 | 124940913 | 124943093 |
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Enhancer Sequence | TGGTAACACA GATCATAACA GCATAGAGTT GCTCCCAGAG AACTCAGTAG GGATTACTTT 60 ACCCTGGAGG CCAGTAAGCC AGGGAGGTTT CCTGGAAAAA GAAAGATCTA CTCGGTAACC 120 TAAAAAAGAA CAGACGAATG CAGCAGGGTT GGTAAGAGTG TTAAAGGCAG AGGGGACAGC 180 ATGTGCAAAA GGATTACAGT TGGGAGAAGA CATGTCATAA ATAGGGAGCT CCAAGTAATT 240 CAGGGGCATG AGCTAACAGT ATGAAAGGAG ACAAAGGGCA AGAGACGAAG CCCGAGAGAT 300 GGGCGGGGTG AGGACAAAGG TTATGGTTGT CTTTCACCCT AAGGCAGTGG GGAGCAAGGG 360 AAGGCTTTAG GCAGGTAACA TAGTAACTCA TTTGTTCTTT AGAAAGACTT CTTTGATTAC 420 ATATAGAGAA GAGGCCAAAG GAGATCAGAT TAGGTAGGAG ATCCTTCTGG TAAGATGATG 480 GGAGAGAGGA GCATGTGAAG GGCATGGGCT CAGGGTGATG GGATAGGTGA CCTGGGATCC 540 TGGTCCTGGC CCCAGCTCTC AGGCTGCCTG CTGGATGACC CTGGGCCAAT GCCTTCCCTC 600 TCTGGGCCCC TTTCTCTTCA TCTTTAAAAT GAGAGAGTTG AACTGGATAA TTTCTAGGGC 660 CCTTCCAACC TTAAGTAAGA GTCTATGATG GAGGAGAAAG GTAGCCAAGG AGTATTTTGG 720 TCCTGATATT ATAGGACAGA TGAAGTTTGG AGTGTCCTGA AAACCACTAA AAAGGAGTCT 780 CTGTTTGTGG CCACCTAGTC ATTACCCCTG ACTCACCTCA CCCTGTGAGG GACTGATTCA 840 GGCTTCTGTC CCTCTTCTGT TTTCCCCAGG GACCTCTTTC TGCTGCATTC CAATCTACCC 900 CCACAAACAG TGCTTCCTGT TGGCATCCTG AAGGCGCAGG CTGCTGGGCC TCTGGGCCTC 960 AGATGGGTGA CTGAGGCCAT CCCAGAGTAA ACACAGGGGC CTCAGCCACT GCTATTATGA 1020 AGCATATACC ACCTGGGTGG GTCAGAGCTG GGAATGCTTA TTGTACAGCA GGTCACGGGC 1080 TGGGCCACCA GCAGAAGAGT CACCTTTGCT GTGAGAATTT AAATCCATCC TTCTATGTAT 1140 CAAAATTCTT TGAACATCTA CTGTGTGCCA GGCTTTGGGG TTCAGGGCAG GCAACATATT 1200 CTCTCTAACT ATAGCTCTCA AACCTTCGAC CCGCAGTAAG GAATGTTTTA CATCATGACC 1260 CAGGATACAC ACAGGTGCAC ACGTGTGATG TATGTATCTT TGTACATGCA ACAATCTATG 1320 ACATTTTCTT 1330
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