Tag | Content |
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EnhancerAtlas ID | HS045-48358 |
Organism | Homo sapiens |
Tissue/cell | Fetal_lung |
Coordinate | chr4:1011600-1012620 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MYCN | MA0104.4 | chr4:1011773-1011785 | GACCACGTGGCC | + | 6.52 | MYCN | MA0104.4 | chr4:1011773-1011785 | GACCACGTGGCC | - | 6.52 | ZNF263 | MA0528.1 | chr4:1012350-1012371 | GGAGGAGGAGGCTGGGGGGTG | + | 6.11 | ZNF263 | MA0528.1 | chr4:1012093-1012114 | AGCCCCTGCTCCTCCTCCTTC | - | 6.17 | ZNF740 | MA0753.2 | chr4:1012144-1012157 | GTGGGGGGGGCGG | - | 7.82 |
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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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Enhancer Sequence | AGCCACCTGG CCACAGGAGG GAAGCCGGGC AGCCCCAGCC CTGCATCCTC TGTACCTGCC 60 CTGGCCGGCC CCCACACCCA CACCGTTCTC CCTACGAATG TCCACTGAGT ATCTGCTGTA 120 TGCCAGGCCT CGGGACACCA CGAGCACGGG AGAGGGGCTT GGGTGTGGGT TTGGACCACG 180 TGGCCAGGAC GGGCCCTTCC AGAAGAGATA TTGGAGCCCC CGAGGAGCTA CGGGGTGAGG 240 GGTGTCGGAG AGGGCACTTC AGATGGGGCA GGTGTTCGGG GAGCTGATAT GAGGGCCTGT 300 GAAGACGGGG AAGGGCAGGC CGCAGGGGGT TCCTGCCTCC GTCCCTCCAG ACTGCAGCTT 360 CTTCCCCTCC ATCCCAGGGC CTGCCCACCT CCACCCTCCC TGGGCCCTGG GAAAGAGGAG 420 CCTCTGTCTG GGGACAGTGT GTGTGTGACA AAGCGTGTAG GCAGAGCGGC CTCTGGGCCT 480 TGCTGCTGTG GGAAGCCCCT GCTCCTCCTC CTTCCCTAGT TGTGTTTTTT ACAGCTGGGC 540 AGGGGTGGGG GGGGCGGCGG GAGGATTTGG AGGCATCCGC CTTCTTGGCG CACTGCCTCC 600 GAGTCTAGTC CTCCATACCT GACAGCAGTG AGGCCCTGTC TCAGACTCAG TTTACTCTCA 660 TGTCTCGCTC CCATGTGGCC CTTGGTGTCC TGCCTGTGCT GGGGGCCTCT CGGCTGTGGC 720 TAAGTGTGTG TGCAGGGCAG GGGCTGTGCT GGAGGAGGAG GCTGGGGGGT GTCTTGGCAG 780 GGTGCACGGC CCCGGAGGTG GCACAGTGCT GCTGTCATGC CCCGGCGGGG GTTCCCTGTG 840 TTTCTTCCTG GCTGCAGTGC GAGGCAGCCG GTCTTCCCAC CAGGTGCCTG TGCCCTCAGG 900 TCCTGACTCA GTTTCCCCAT AGGCTGCGTG GGTTGGACGC CCGTCCAGGT GGCGTGGTGC 960 CCTGGCCGCT GTCCTGGTGT GATCATTCCC CAGGAATCTG GGGGGATGGG CTTCCTCCTG 1020
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