Tag | Content |
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EnhancerAtlas ID | HS051-23854 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr6:108168880-108170250 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr6:108169603-108169622 | TCGCGCCCCCTGGTGGCCA | - | 8.78 | Myod1 | MA0499.1 | chr6:108169249-108169262 | TGCAGCTGTTCCC | + | 6.98 | Myog | MA0500.1 | chr6:108169248-108169259 | CTGCAGCTGTT | - | 6.02 | Tcf12 | MA0521.1 | chr6:108169248-108169259 | CTGCAGCTGTT | - | 6.62 | ZNF263 | MA0528.1 | chr6:108168904-108168925 | TTCCCCCTCCCTCCCTGCACC | - | 6.33 |
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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 |
GH06I107847 | chr6 | 108169005 | 108170204 |
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Enhancer Sequence | ACATGTTTTT ATTTCTCCTC AAGCTTCCCC CTCCCTCCCT GCACCTAAAT CCGTTCCCGG 60 CTAGAGTTGC TAGAAGAAAA ATACAGGACA CCTAGTCAAA TTTGCATTTC AAGAAAAACA 120 AGGAAAGCTT TTTCAAAGTG TAAGTACATC CCAAATACTT CATGGGACAT GTTTATACTA 180 AAAATTCATT TGTTGTTTAT CTGAAATGCA AATTTAACTG GGCATCTTTT TTGGGGTGTG 240 CTGGATCTGG AGACCCTCTT TCTGCCAGAA CGCACGGGCT GTGTGAGGGG CGTCCTACTG 300 AGGGTCGGGC TTGATGGCCC GGGTCGGTTA TATCTGTCCC CCGGCTAGGA GAGGCTCTGA 360 GGCAATAACT GCAGCTGTTC CCCTCCCCCA GGACGGGGGT CGGGGGTCGG GCCTTGGGGA 420 GCCCCCTTAG GAGGCAAGGC GCTAGAAACT AGAGAAGCGA CAGGGACCCT TTTTTTGCGT 480 CTGAGTCCAA GGAGAAACAG CTGGGTCTAA GGGAGACGGT CGGGACTCTG GGTCTGACTC 540 AACGAATGCC GGAGGCCACC CTGAGCTCCA GAGTGGTGGA GTCCGGGACG TGGCTGCGAG 600 GGGTCTGTGG GAGCCGGGGG CACGGCAGCG TCGCTCCAGC CCCACTGGCC GGCCCGGGAC 660 TCCAAGAAGA GGCAGCGGAT CTCCCAGTCC CTGACCAGCC TGGCCGGGCC CCGGTCGGCC 720 ACCTCGCGCC CCCTGGTGGC CACAGAGGGA GAAGCCGCCC GCTCATTTCT CCTGCTGCCG 780 CTGGAATCCG GACTCCGGGG GCTGAGCGCC TGGACCGGAA GGAGGAAGGG AACACGGCAG 840 AGTCCTCGGG GGAGCTAGGG CTTCGTGGGG CAGGAAGAAG ACAGTGGCCG TTTCCACCGA 900 AGACACCACG TGCAGTGTCT TCACAGGCAA AGCAATCCCA GCTGTGAATC CCACGGAGCA 960 CCTACCTGCT CACCAAATTC TGGTGGCAGA ACGAAGCCTC CGGTTGACGT CCCCAGGGGA 1020 GATCCCCCGT CGCTCCTGAG AACACCTTTG CCGACTCCCC TCTGCAGGCA TTAGGCCATT 1080 GGGGAACTGA ATGCTTTCCT GGCCCCACCA GTTAGCCACC TTGTGTGATA CGGAAATCTC 1140 ATCTTTTCAA ATATAAGACT TGTCAAGCTG TAGGAAAAAT ACATGTGAAC ATCCTCCTCA 1200 CTCAGCAGTA ACATCCTCAG GCTCTTGCAG CTAACCCAAA ATGAAAAGAT CGAGGTCTGA 1260 AGACTTGGTT TACATTATTC ACACAATGAT TTCATCCTCT TTCCCCTTCC CTCAAGGCTG 1320 TGGGAATGTT CTCTAAGAGG TGGAAGAATC CAGACTCAGG TGTTCTGAGT 1370
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