Tag | Content |
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EnhancerAtlas ID | HS091-10613 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr12:100548120-100549300 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr12:100548710-100548729 | TGGCCACTAGGGGGCAGGG | + | 7.62 |
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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: 2 | ID | Chromosome | Start | End |
GH12I100155 | chr12 | 100548378 | 100548579 | GH12I100154 | chr12 | 100548601 | 100548830 |
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Enhancer Sequence | GCCCTGTTCT ATAAATACTC ATATATATAT ACATATACAC ACACACATAT ATGTATATAT 60 ATGCATATAT ATACATACAC ACATATGTGT ATATATACGT GTGTGTGTGT GTACATATAT 120 GTATACACTC CTACACATGG CCGACTGCCT CGCCTCTAGC GCTGGGAATC AGTCACCGTG 180 CTGTCCTTGT GGAGTCTTGT GACCCAACTA CAAGAGAACA CTGTCCCCCA ACAATCCCCA 240 TCCAAAGTCC ATCACCTCCA GTGAGCCTCC CTGTCATGCC TGGCCTGTGG ACAGCCAGTC 300 CCCACCATCC CTCCTGCCGC CCGACAAGCT TGGGGGTGCT GTGCAGACAG CTGTGTGGCC 360 CGACAGTCTC TACCAGTCCT GCTGTCCCTT GGCTGGGAAT AAAACCCATT TCTAAGTGAC 420 GGGGAATGTG TCCTCTGCTG GTTGCGTTCT CTGTGGAGCT CAGGGGAGGG GAAGGGTCAA 480 CCCATTACCA GGGTGCTATT GGGAGTGGTA AAAAGGCCAC ATCCTTTCCA AGGGACGCTT 540 CCTGGAAAGC CTCCGGAGCT TAGCAGGCTC TCATCCTGTG AAGCCGGCTC TGGCCACTAG 600 GGGGCAGGGC CATGAACTCA GATTGGAGGA AGCCTGTGGG GCAGCTGGCA ATCTAGAGGG 660 ACAGACAGAA CAGGCCACCA GGTGCAGACA GGCGAGGGAG GCAGGAGAAC AAAATGGAAG 720 ACAACTGGGC TGGATGGAAG TCAGTGACCT TGGATGCTGG CACCTGCCTT ACTTGCCACT 780 GCTAGATCAG GCTTCCGAGC CTGTTAGCCG TCCAGGCCCC ATGGTCACCC ATAGGTGCCA 840 TGGCAGTTCC TGTGGAATTC CCCAGGTGTT ACCAGGCAGC ATACAGGTAA CAGGCCTGGA 900 AGGTCCCCAA TACCCCAGCT GGACATGCTC ACTTTGGGGC TCCCTGTTCA GTGGCACAAA 960 CTCCATGACC CAGTGAGGGA AACAGGAATA CACCAGGCCA AGCAGTATAT GGCTAAATAC 1020 ATTCCAAAAT AAAAAGCAAA ATAAACAGGA GTCGCATCAC CACAGTGCCA CGACCCCATC 1080 TCTGCCCCTT CCCCTGGCCT ATGCTATCAA TAAATAAGTT TTCCAGCCCC AAATAACTAT 1140 CAGAACTTCC TACCCATATG CCAGCTCCAA CCTCTGCTAT 1180
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