| Tag | Content |
|---|
EnhancerAtlas ID | HS098-14719 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr12:120538110-120539990 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr12:120539302-120539323 | ATGCAGTTTCAGTTTCTCTCT | + | 7.22 | | IRF9 | MA0653.1 | chr12:120539306-120539321 | AGTTTCAGTTTCTCT | - | 6.28 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_27057 | chr12:120537449-120541185 | Esophagus | | SE_31982 | chr12:120538202-120540645 | Gastric | | SE_41982 | chr12:120537882-120541422 | LNCaP | | SE_68937 | chr12:120538843-120541016 | H9 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I120099 | chr12 | 120536948 | 120540903 |
|
Enhancer Sequence | TCTCTGAAAG GCTGGCCCTT GGGAAGGTGC CTGCATTCAC CCTGCCACAC CTTGCAGCTT 60
CAACAGTTAT AGCACACAGG TGGCTAGTCC TTAACTGGGG TGGTCATGAG GAAGAAAGGA 120
GCTAAGCATT ACCCCAAGGC GGGGGAGCAG TAAACAGTCA GTATGCGTTC TTCAGCATCA 180
TCAATGTGCC TTCAAGGACA ATCTGTGGTC CCAGACAGAG GTGGTGGAAG GAAACCAACA 240
GGCAGCTTAG GGGCAGCCCT GAGCATCTTC CCTGATGCTG CAGAGCCAGA GCTCCTGCCC 300
AGCCCTGGGA CAAAGCCCAA CCTGCCCCTG CCACCGCCCC TGCCCCATCC TTGCTCCATC 360
CTCAACACGA CCGCTGGGAT CTCTTCCCAG GGCTTCATTC TGCCCACAGC TTTGCTTCCA 420
GGGCAGCGTC GCTCCTTGGC TTCGGGGTAG CTGTGACGAT CAAGCTCTCT TGGCACTGGG 480
CCCAAGAACT AGCTCTGGCC TTGGCAGCTG CTGCTGAGAG CGCCGGGTCA GCACATGGCA 540
TGGTGTGTCA GACGCCTTCC AGAGCGAGGG CGCGCCGGAG CCACAGGAAC AGGCGACTGT 600
CCCCTGCCAG CAGAGGAAGC CCAAGGAGCG GATGGCTCTG CAGACTCTCC TTTGCTGAAG 660
ATGATCAGAG ATGCCAAGAA ACGCCTGCAG CCATGGCCCC GGCGCACAGC CCCCGCGGCT 720
CCCTGGGCGC CTCTGCCTCA TCCGGGGCCC AGGAAAGGGG CTTTATCTGA GAGCAGAGAA 780
TTTGTCTGGG GATGAAGTCA GGGGCTCAGA GCTCTGGCTA GGAGGAACCG GAGCACCGAC 840
GTTTCCCATG GCCACCAGGA ATCACCTTCA CTCACAGGGA CTCTGCTCTA GGCCAGGCAC 900
AGAGCTGGGG GCTTGGTATC CATTACCTTA TTAATGTCTG CAGCCACCTG ATCCAGCAGA 960
CCTCAGGATG GCCATGTGAC CAGCAAGGAC GTGAGGCTGA GTGCAGCGGC CAGCTGGAAG 1020
TCCTGGCGCC CAGGGCTGAC TCCCAGGCCC AACGCCAGGG CCTTGCCTTC CTTGTCACTT 1080
CTCCCCTCAC CTCCATCCCA CCCGCACCTC TCAGGGCCGG CAAACCTCAG CTTCTGAGAG 1140
CAAGAACCCG AGAAGGGGTG ACCACAAGGC TTTTTCTCGC CAGGCTAACA GGATGCAGTT 1200
TCAGTTTCTC TCTGAACGCC CTGCATCGGA AAAAAGTCAC GCTACTGCAT CCTGACTGCC 1260
CTATTCCTGA AAACTCCTCA CCTCCCCAAA ACTCCTTCCT TCTTTGCCAG TGACCATCAA 1320
AGGGCGTCGA GACTTCCAGT GGCCCCTCAG GGCGCCCTGC TGGGCCTCCT GCCTCATGAG 1380
GGCCAGAGCG GGACTCTAAG ATGGAGCCAC CTGTCTGCTT CCCCAGACAC GTGGGACGGC 1440
AGCAGGGGCC CAGCCGCTGC CCACAGGCCG CCCCTTCCCA AGCCCCTGGG GAAAAACCCA 1500
TGTTGCTCCC AGGAAGCTGA GTGACTCCTC CCCGCCTCCC CACGGAATGG AGGAACCAGT 1560
TCACCTTCTT CCCGCTCTGC CCAGCCCAGA AAGCAGCTGA CTGCATGATG GCAGGGAGGG 1620
GCTGTGGCTC CTCCTGCTGA AAGAGCCTCG GACCCCCCAG GCCCCACTGC CCTGCCCAGG 1680
AGTTCATTCC TCATGGCCAC GGGCCTCTGA ACCTCTGCCA CCCTGAACCT CCGCCTGGTT 1740
TTAAGGCACA GGACGGGGCA GGAAGGCAGG GGCGCCACCT GCCCAGTCGA TGCAGGGCCT 1800
CGGCAGACTC AGGGCCAACC CTGAGTGCCC CCAACCTCTG CCCCACTGAG TTAGGAGGCT 1860
TCATCCTCCC TGGGCCTGTT 1880
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