Tag | Content |
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EnhancerAtlas ID | HS092-19256 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr16:27770350-27771220 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
BHLHE40 | MA0464.2 | chr16:27771088-27771098 | ATCACGTGAC | + | 6.02 | LHX2 | MA0700.1 | chr16:27770402-27770412 | GTTAATTAGT | - | 6.02 | MITF | MA0620.2 | chr16:27771084-27771102 | GCAAATCACGTGACCCAG | + | 6.08 | MITF | MA0620.2 | chr16:27771084-27771102 | GCAAATCACGTGACCCAG | - | 6.08 | TFEB | MA0692.1 | chr16:27771088-27771098 | ATCACGTGAC | + | 6.02 | USF2 | MA0526.2 | chr16:27771086-27771102 | AAATCACGTGACCCAG | - | 6.24 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr16 | 27770548 | 27770945 | chr16 | 27770598 | 27770827 |
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| Number: 1 | ID | Chromosome | Start | End |
GH16I027759 | chr16 | 27770334 | 27772150 |
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Enhancer Sequence | AATAGTTTTC GTTTGTCTCA TTTACTTGCA GATATCTACT GAAGCCCTAC TTGTTAATTA 60 GTCATGTGTT TAAAATTTTT ACTAAAAACA TTCATTGAAC ATCTACTAAG CACTGTTCTG 120 GGCTCCGGGG ATACAGCAGT GAACAAAACC AGCAGAGTCC TGGCCTCAGG GAACTTCCGT 180 CTTAGTGGGG GAGACTGATG GAGACAAATA AGCAAATCAA TGTAGACTCG ATTGTCAGGA 240 AGCATTCAGT GCTATAAACA ACAAGGCGAG CAGGGTAAGG ATGTAGAGAG TGATGGGGTG 300 AGCAGGGCTG TTTGAGCTCT GGTTATTAGG GAAGGCCTCT CAGGAAATGA CATTGGAACA 360 CTGACTCATG CTGAGAAGGA ATGTGTCAGC TAGCTTTTGC TGCCGAACAA GCCAATCCAA 420 AATCCACTGG CTTAACACAA CTACCATGAA TTATATTCAT GACTGACTGG TAATTCAGTA 480 TCTTGGCTGG GCAGCTCTGG GTGAGCCAGC TTGGTTGGCC TCTACTGGGC CTGCTCGAGT 540 TCCTGATCAG CAGGGAGGTG GACCAGCAGC TGAATGACCT AGGACATCTT CACCCACCCG 600 TCTGGCAGTG GGGAGGCTGC TGGCCAGAGA GACAGGTGTC TGGGTTAGCT GGGCTGCCTC 660 GCATGGCAGT CTCAAGCCCC GAGTGCTTTA CAGGCTCTGC TTGCCTCACG TGGGCTTCTG 720 TCCCAGTGTT CAAAGCAAAT CACGTGACCC AGAGTCAGGA GCAGAGAAGG AAACTCCAAC 780 TCTGGATGGG ATGAGGGGCA AAATCACATT GCAACAGCAG GGACACGGGA TGGGACGAGC 840 TTGTAGCCAC TTTGCACGTG AATGATGCGG 870
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