Tag | Content |
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EnhancerAtlas ID | HS051-22354 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr5:138897080-138898180 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NHLH1 | MA0048.2 | chr5:138897574-138897584 | CGCAGCTGCG | + | 6.02 | NHLH1 | MA0048.2 | chr5:138897574-138897584 | CGCAGCTGCG | - | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr5 | 138897527 | 138897822 | chr5 | 138897122 | 138897400 |
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| Number: 1 | ID | Chromosome | Start | End |
GH05I139517 | chr5 | 138896810 | 138898710 |
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Enhancer Sequence | ACAGTGCTAC TGCACTCCAG CCTGGGCGAC AGAGCGAGAC TCCGTCTCAA AAAAATAAAT 60 AAATAAATAA ATAAAATAAA TAAATAAATT TCCTTCCTCC AGCTGCAGGG CAAAAAATGG 120 GTTGAAGAGC CGGACTGGTG GTAACTGGTG TGGCCATCCA GCCTGGAGTC GATGTTGGCA 180 TGAATGAAGA CACAGGCAGT TGGGACAGAG AGAAGCGAGT GGGATGTGGA GGTGACCCGA 240 TGAAATACTG GCCCGGAGAT ATGAGGCATG AGGCGGGGAG CACGAGGGTG TCGAAGGGCC 300 AAAATGTGGT AAGAGAAGCC GGAGGAGTGT GAGGACAGGT GGAAGGGATC CAATGTGGGA 360 TCTAAGGGGT CTGAGACCAC CGTGGCCGCG GGAGGCAGGA GAAGGTACCG CAGAGCTCCC 420 GGTGATGTGT CAGGAGGCCC TACACTCGCG CGTGCACTGG CTCGCAGTTT GGACAGAGAC 480 CCTACAGGCC AGGCCGCAGC TGCGCCCAGA CCACCCCCAG CGGGTGAAGA CTGCCGCGGC 540 GGCGCAGTTC CCGGCATGCC TCCGGCCGGT GACTTCATCC GGCCCGGGGC CAAGGCCCGG 600 CCTCCGCTAG AGGGCGCTGC TCTCAGCAGC CGCGCCGCCC GGATGGACTC GCGCCAGAGT 660 AGGACAAGAG AGGCAGGCGG CGGCTGCTCC GTGCGGCTCC CACGCCTCTC GGGCGGCAGG 720 TCCTGCCTCG GACCTGGGAC CACTGGCTGG CGCCTGTGGC TCACATCTCC ACGCCTTTGC 780 CCGCTCCTCC CAGGAGCCCG AGTCAGAAAC CTGTGCTTCA CCCTCGAGAG CGCTGCCATC 840 CTCCCCCTCA ACCAGACGGG CATGGCGTCT GGTTGTCCGT CCTGTCTTCT CATCGTCTCA 900 GAGCCCTTCC CTGACCCCTA CCCTCTCTCA GACCAACAGG ATGATGACAG GAAGAGGATC 960 CAGGACCAAC TCCTAGCGGT GACCTTGAGA AAACAATCTC ATACCCCAGT TTCCCTTACA 1020 ATGCAATGGA AATAATACTA ACAACCCTGG AAGAGTGTTG GAAGGACTAA ACGAAATCAT 1080 CTTTTTCAGT ACTAAGCAGA 1100
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