Tag | Content |
---|
EnhancerAtlas ID | HS187-17708 | Organism | Homo sapiens | Tissue/cell | Th1 | Coordinate | chr3:137784290-137786070 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TFAP2A | MA0003.3 | chr3:137785978-137785989 | TGCCTCAGGCA | + | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CACCTTGTCC AAATACCTCA TTTTATAACA AAGGATCAGA AACCACCTGC ACAAGGACAA 60 GCAGGTAGTA AGTGGCAGAG CCAAGACTTT CTCTGAAGAT TCCTAACACC CAGTCCCAAG 120 ACCTTGCCAC CCTATTGCCC TTGCCTGGTG GGCATCGATA CTTCTCCAAA GATCTGTTTC 180 TGGTGAATTC TGATGGACTG GCAGGCTTGG CTTATGCTGT AAACATGGCC AAGTACTGCA 240 GAGTCTATTA AGAGCAAGAA ATTTGCAGAC CGCAAGCCTA GCCTGACATC CCAGGGTTTC 300 TACTTACTGA CCTTGGAAAG ACAAAACTCT AAATTCCATA TTCTTTAACA CAGCCTTGGC 360 TAGAAAATAC AACTGAAGCC AGAAGCTACA GGCCTCAGTT GGCAGTTTTA TAGGAAAATC 420 TTGAAAGAAT GGGAGTAGAC AGTTGTTTTG AAAAGAAGGA GGCTCAACTA GTCATTGCAA 480 CCTGTTAGAT AGAAAATAAT ACGTTTAACG AATATTTTCA TTCCACTTAC CATGACAGTT 540 AGCTCAGGTC TCTACAATGC CCTTTCCACC AACAAGTTGA ATTTCTAAGT CTCTTGGCTG 600 AAAAGGGCAA AGAGCTTTCC TGTATGATGA AACAGGCTGC ATGGCCCAAA GGCAGCCTGC 660 TATAAAGGTT GACTGTGGCT GCCTCCTCTG TCTCAAGCTT TGCTGGGAAG CCACATTTTT 720 CACAATTGAG TTGTTGCAAA AAGTTATGTG TGTTACACTC TATGTGTTCT TGAAAACTAT 780 ATTTGTCAAA ATGTTCATGG TAGGAAACTG TTTTCCCTTC AAGTTGTAAC TGAGGTTTAC 840 CTTGGAGGCT ACTTTGACCA CTGTGATATT TAACTCTATG ACCACCAACT CTTGATCTGG 900 TGCTAATGAA CTCAAACAGC ATTAAAGACT ATGGGGATAT TCTTAACATT GGGAACACAG 960 CTAAAGGCAG CTCTTTCTGG GGGGAAAAAT GGTTTACAAG TAAATAAATA AACAGTGACT 1020 CTAACACATT AACTTCAAAA ACATCATACA GAATCTCAAC TTGCCATGAC ATCGTTCTGT 1080 GGTCTTGGGC CAGTCATAAT GTCTATGAGG CTTAGTTTCA ACTTCTGTCA CGATGTGTGT 1140 GGCTCAGCCT TCCCTCATCA GTGCTGTGAG GAGTAAATGA GGAGACTTGT GCGAAGAGAT 1200 CCACACAGAG CTGAGCACGC GGTGAGCACC CAGCAACACC AACATAGAGG GGAGAGCCTT 1260 CTCTCACACG CCTCGAGCTT CCACAGAAGA AGGAACTTCT GCTCTACTCA CCGAGATGGA 1320 CAAGGATAGG AGAAACACCC TCCCAGTTTC TTCCCCACAT ACTACCCTCT CTCACAGAAG 1380 AAGCCAAGCA GAGGGGTGGG CCTACAACAC ACCCTGGGCC ACGGCGCACC TGAAGGAGGG 1440 CCGCTGATCC AGAAGACAGT GCCAGCTCTT TCTCTCGGAC CCTCCCCGCC CCTGTGGCTG 1500 GGGTTGGAGC CTGGCTGGAG TGTACCCTAC AGCTGCCTGT TTAAGGGCCT GCACACTCAG 1560 GGTCTTCTTT GCAAACCCAG CCCTGCACAC AAGTAAGATT GGGATCTGGA TTTGGGGAGG 1620 CTGGAGGGGC CCCCACTTTG GCCTCAAGTG CGGGTTGTTC CTCTAATCCA GCCCTAACAG 1680 GAAGCCTATG CCTCAGGCAT TCCTGGGCCC TGTCACCACT ACTAGAGCGA GGCTTTGATC 1740 TCCCGTAGCT GGCCACAGTG TTTACTCTCT ACTGGAAAGA 1780
|
| |
|
|
|