Tag | Content |
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EnhancerAtlas ID | HS188-06696 |
Organism | Homo sapiens |
Tissue/cell | Th2 |
Coordinate | chr19:49100180-49101690 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Zfx | MA0146.2 | chr19:49100843-49100857 | CCCGCCTCGGCCTC | + | 6.01 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr19 | 49100408 | 49100673 | chr19 | 49100679 | 49100762 |
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| Number: 2 | ID | Chromosome | Start | End |
GH19I048596 | chr19 | 49100058 | 49100257 | GH19I048597 | chr19 | 49100441 | 49100590 |
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Enhancer Sequence | GGGGGTTCTG GGGTTCAGAG CCCACTAGGC CACTGCCCGG CTGTGTGACC TGGGAGAGTT 60 ACTTAACCTC TCTGGGCCTC AGTTTCTCAC CCAGCTGTAA CATTGGGTGA ACAGGGTCAC 120 TGTGGCCCCA GGGTTGATCA CGCACGGGGC TTAGCACTGA CTCAGCACAC GTGCCAGCCA 180 CCCGAGGCGT CCCCATCCAG AGAACTCCCA ACGACAGCAA AACATCCAGG AGTACTGCCA 240 ACGCCAGGTT TACCCGAGAG AGATTTAGAG TCTTCATGAG TCCTCCTCGA CGGCCATGTT 300 CACGGCAGAA ATACTCAAGC CCTGGGTTAC GGGGCGCAGG CGGTAGCATA GTTGTTTCCT 360 CTTCCTGCTG TAACAAAAAC ACCGCAAACT CCATGACTCA AAACACGTTT ACTCTTTTTT 420 TTTTTTTTTT TTTTGAAAGA GTCTCGCTCT GTCGCCCAGG CTGGCTGGAG GTTGCAGTGG 480 CGCGATCTCG GCTCACTGCG ACCTCCACCT CCCAGGTTCA AGTGATTCTC CTTCCTCAGC 540 ATCCTTAAGT AGCTGAGACT ACAGGCACCT GAAACCATGT CAGGTTAATT TTTGTATTTT 600 TAGTAGAGAT GGAGTTTCAC CATGTTGGTC AGGATGGTCT CAATCTCCTG ACCTTGTGAT 660 CCACCCGCCT CGGCCTCCCA AAGTGCTGGG ATTACAGGCG TGAGCCACCG CGCCCGGCCT 720 TTTCTTTTTT CTTTTTTGAG ACGGAGTTTC ACTCTTGTTG CCCAGGCTGG AGTGCAATGG 780 CGCGATCTCG GCTCACTGCA ACCTCCGCCT CCCAGGTTCA AGCAATTCTC CTGCCTCAGC 840 CTCCCAAGTA GCTGTGACTA TAGGCACCCA CCACCACGCC TGGCTAATTT TTTGTATTTC 900 TAGTAGAGAC AGGTTTTCAC CGTGTTAGCC AGGATGGTCT CGATCTCCTG ACCACCCGCC 960 TCTTCCTCCC AAAGTGCTGG GATTATAGGT GTGAGCCACT GCGCCCGGCC AAGTGAAGCA 1020 TCTTCTAATC TCTGACCCTC CTCCCTTCTA TAGGGACCCA GGTGATGACA CTGAGCCCAC 1080 CCAGATACTT CAGGGTCCTC TCCCCATCTC CAGATCTTTA GCTTAATCCT ATCTGCAAAA 1140 TCCCTTTTGC CACATAAGGT CACATATTCA CAGGTTCCAA GGATTAGGAC GTGGATATGG 1200 AGGGAGTCTT TATTCAGCCC ACCCCAGGGA ACCCCTCCCC ACAACCTCAT TAAGGGTGCT 1260 GGGTAACATG GGGCACGTGC ACTTGCCAAA AGGCAAACTA CGGTCCTCTG AATGCCATGA 1320 GCCCCAGGTT TCCAGGTGAG GGGTGATGCC CCTGTGATAG CCCCACAATG AGAAAACTGA 1380 GGCTTGGGAG GGGTGCCGTG GCTCACACCT GTAATCCCAG CACTTTGGGA GGCCGAGGCA 1440 GGTGGACCAC CTGAGGTCAG GAGTTTGAGA CCAGCCTGGC CAACATGGTT AAACGCCATC 1500 TCTACTAAAA 1510
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