Tag | Content |
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EnhancerAtlas ID | HS080-00501 |
Organism | Homo sapiens |
Tissue/cell | H9 |
Coordinate | chr1:22676690-22677590 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF16 | MA0741.1 | chr1:22677408-22677419 | GCCCCGCCCCC | + | 6.02 | KLF5 | MA0599.1 | chr1:22677408-22677418 | GCCCCGCCCC | + | 6.02 | SP1 | MA0079.4 | chr1:22677405-22677420 | CTAGCCCCGCCCCCC | + | 6.67 | SP2 | MA0516.2 | chr1:22677404-22677421 | CCTAGCCCCGCCCCCCT | + | 7.39 | SP4 | MA0685.1 | chr1:22677405-22677422 | CTAGCCCCGCCCCCCTC | + | 7.14 | ZNF263 | MA0528.1 | chr1:22677426-22677447 | CCTTCCCCTCCTTCCTGCCCC | - | 7.23 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 22677022 | 22677200 | chr1 | 22677200 | 22677422 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I022349 | chr1 | 22675891 | 22678331 |
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Enhancer Sequence | CGCCTCTGCC TTCCGCACTG GGATGCTGTT CTCATGGCCT CCCTTCTGCT CTGCTCGGCT 60 CACTGCTGTC ATCTCCGCCT GCATCACGTT AATTACAAAT CTTGGCGCTT TCAGATCTAG 120 CTCGGGAAAG GATCTCAGAA GTTACCCAGT CAGAGAGGCA TGCGCTGTTT CTGTCCCAGA 180 GAGGTATAAC CCAGGTCTCA GCAGAACCTG GCATACACTC TGGATGTGGC TTCAGCCCTC 240 TCAGGGAGGG CACCACTCCT GGATGACTGA GCCAGGGCGC GAGCCCCAGG GAAAGGGGGA 300 TCAACAGACC CAGGAACTCG CACTAGCTCA CCCCAGCAAG GGGAGGGGCT GGCCCAGGGG 360 CCCTGCTGGC AGAGCCGGCC AGGCTGGGAT TTATGGGCCC CTTTTGGACA CGTTAAAGAT 420 CACATTAAGT GCAATAAATG TAGATCACGC TCCTAAATAA GCTGAGATTT ATCCCCGGAT 480 CCTCTCCGCA GGGGCCAGCT CCATAAATCC TGCGCGACCC TGTCCCCTGG CCAAGGGATG 540 GGGGAGGGGA GGCCAGAGTG GGGAGGGGCG AGGTGTAGCA GGGCAGTTCC AGGTACAGAA 600 GGATGGAGCT GAGCAGGGGC TGCAACAGGG GCCAAGAAAG GGGGCAACAG TGGGCCCAGG 660 CGGCCTGCCC CTGACCTCCC GCTCACTTGC CCAAGCTCCT TACCCCAGCC CTCTCCTAGC 720 CCCGCCCCCC TCGCATCCTT CCCCTCCTTC CTGCCCCCTC CCCCGCCCCC ACCCCGCCCC 780 CACCCTCTCT CCTGGCCCCT GCCTGCCTAT AATCTCGTTC TTGACATTAA AACAATATAA 840 TGACTCCACT GCTGGAAAAG ACAAGCATCT GTAGCTTCTA AATGGGCAGC TCAGCCACAG 900
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