Tag | Content |
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EnhancerAtlas ID | HS022-07609 |
Organism | Homo sapiens |
Tissue/cell | CD4+ |
Coordinate | chr19:48660720-48662210 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myod1 | MA0499.1 | chr19:48661943-48661956 | GGGGGCAGCTGCT | - | 6.03 | USF2 | MA0526.2 | chr19:48661193-48661209 | TCAGGTCACGTGGGCA | + | 6.24 |
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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 |
GH19I048157 | chr19 | 48661256 | 48662368 |
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Enhancer Sequence | GACGGGGTTT CACTATGTTG GCCAGCTCTA CACAATGGGA TGTCAGGGGA AATGATGTAC 60 ACCTCTTCGT ATAGTTTTAT TTTTATTTAT TTATTTATTG AGACAGGGTG TCATTCTGTC 120 GCCCAGGCTG GAGTGCAGTG GCGCGATCTC GGCTCACTGC AACCTCTGCC TCCCAGGTTC 180 AAGCAATTCT CCTGCCTCAG CCTCCCGAGC AACTGGGATA ACAGGCGCCC GCCACCACGC 240 CCAGCTAATT TTTGTATTTT TTTTATAGAG ATGGGGCTTC ACCACGTTGG CCAGGCTGGT 300 CTCGAACTCC TGAGCTCAAG CGATCCTCCC GCCTTGGCCT CCAGAGCACT GAGAATACAG 360 GCGTGAGCCC CCGTGCCCAG CCTTCTCTCC ATACAGTTTA GATGTTTGTT CCCTCCAGAT 420 CGCATGTTGC AATTTGGTCT CCAATGTTGG AGGTATGACC TGGCGGGAGG CATTCAGGTC 480 ACGTGGGCAG ATCCCTCATG AATGGCTTGT ACCCTCCTTG TGGTAGGAAC CGAGTTCTTC 540 CTCTCCTGGT TCACATGAGA GCTGGTTGTT TAAAATTCCT CTCTTGCCAT GTGACACACC 600 TGCTCCTCCT TCACCTTCCA CCATGACTGG AAGCATCCTG AGGCTCTCAC CAGAAGCAGA 660 TGCTGGCACT ATACTTCTTG TATAGCCTGC AGGACCGTGG GCCAAAATAA ACCTCTTTTC 720 TTTATAAATT AACTGGTCTG AAGTATTCCT TTATAGCAAT GCAAAATGGA CTAACATGCA 780 TTTCCTGGTT CAAATAACAT CCACTTAATG TTGAGTGGGG TGCCCTCCTC TTCCTGTTGG 840 CAGAATATGG ATGTTCACAG GGACAAGGGC ATCTACAGAG AGCAAACGAC AGCACAGAGG 900 AAGCCTGGGC CTCTGACCCT GTGAGACGGT CACATGAATC CCGGACTCTG CACTCAGGAG 960 AGAGAAAAAT AAGTTTGCGT CTTGCCTAAG CCACTGCTAC CGTGTCTCGG TTTCAACCAC 1020 TCACTTATCT TCTTACAGGG CCCTGTGCCA GTTATTAAGT GATTTTCTCT CAGCTCCAAA 1080 CCTGTCACTG TCCAGTCTCC TTCATGCTGC CAGGACCGGG ACTCCACAAA TCTTCTTCTT 1140 GCTCTGGCGC CACCTGGGCA TCAGGCAGTG CCAATGGAGG GAAGCAGAGG GCACTGCATG 1200 ACTGGAGGCA CAGCCGGCTT GCCGGGGGCA GCTGCTGGAT CCCACTGACA GTTTTTTCTA 1260 ACATTCACGG GGCTTGCCAC GTGGTACCTG ATCAGAGACC CTGGCATCTC CCACCCAGTG 1320 CTCCCTTCCT GAAAGATCAG AGTTGCAGGC TCTCGGGGCA CCTTCTCTAA GCTCAGAGAC 1380 CTGCCAGCAG TCCCACCACA GAGGTGTGAA TTTCAGCTCA AAAGCCACAG GGATGGTCAC 1440 TGCACCCCAC AGTTGCTACC TCCATGATGC CTTAGAGTTA GTTCTCTTTT 1490
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