Tag | Content |
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EnhancerAtlas ID | HS091-27584 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr2:132279150-132280410 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HOXA13 | MA0650.2 | chr2:132279785-132279796 | GCCAATAAAAC | + | 6.14 | MYCN | MA0104.4 | chr2:132280143-132280155 | GACCACGTGGCC | + | 6.52 | MYCN | MA0104.4 | chr2:132280143-132280155 | GACCACGTGGCC | - | 6.52 | TFAP2C | MA0524.2 | chr2:132280229-132280241 | TGCCCCGAGGCA | + | 6.14 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr2 | 132279400 | 132279600 | chr2 | 132279383 | 132279433 | chr2 | 132279991 | 132280236 |
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Enhancer Sequence | TCTGGCACCT GGGCTCAGTC TCTAGGAGGT TCACCTATAC AGAGTCCCTG AGCACACGGG 60 GGCTGCAGAA ACAACTGTTG GGCACCCTGT CGGCCCCTCC CCCCAGTGTC CACAGGCCTG 120 GGCCTCTGGC TTCCTATGCT TTCCTCTCTC AGAGGCACAG TAGACTTTGC CCTGTCTTTA 180 CAAAAGATTC AAAAAGTTAG GCATGGTGGT TCACATGTGT GGTCCCAGCT ACTTGGGACG 240 CTGAGTTTGG AGGATCGTCA GGGTCCAGGA GATCAAGGCT GTAGTGAGCC TTCATCACGC 300 CACTATACTC CAGCCTGGGT GACAGAGTGA GACCCTGTTC TCAAAGAAAA GCTGACCACC 360 GGGAACATGT GCCGCCAAGT CTATGGCTTC CAGAAGCTCC AAGGATTGCG GGAGTTGCTG 420 GGGGCTGAAC TGTCTGGCCA GGAGTGGGGG GCAGGCAAAA ACGCACTGAG AACCAAGAAC 480 AGCAAAGCTG AGTGAGGGGT CAGGGTCCTG GGGGCTGGGA CCTGGACAGC GATGGCCACA 540 AGGCCAGCTG GTGCTCAGTG GCTTCTGCCT GGGGAGCAAG GGCAGCAGCG GGCAGCTAGG 600 TTCCAGCCAC TTCCAGGTAG CAGGGTAGGG ACCTCGCCAA TAAAACGGGA TTTAAATTTT 660 GCCAAGAACT TTCACTGTAG AGAAAATGGG ACTGCTGGGA TGAGAGCAAA ATGCAGTTGG 720 TGGGGCCCGG CCAGGAGGCA CTTGTGAGGG ACTTCTGGGG AAAGACTGGA GTTGGAGCAA 780 CTCAGGGGAA GCAGTTCTGT CTGGGGCACA AGGAGGAGGG AGGCCAGGCT GGAGGCAGGA 840 GCTCCTGCAC ATTCTCGTCT CCACCCCTGG ATGCTTCCAG AGTGGTTTGG CCTAACTGCC 900 ACTGCCCCCG CCTCCTCAGC TCCTAGGATG CCCTTGACTT TTTGCCATTG GGCCACACTC 960 CCCTGCTGAC AGGCCAACTC CAGATGCTTT TCTGACCACG TGGCCCAGAG CCTCTGGCAG 1020 CGCAGCTTCA GGCTGTCCTG ACACCACCCC TGCCCCTTGC ACCTCCGCAT CGTCCTCCTT 1080 GCCCCGAGGC AATCCCATTC CCTGGATCCC ATTCGTGGCC CACTCCCACG ATCTACCGCT 1140 AGGATATACC AGCGCCCCCG TGATCCGAGG TAAGTCAGAT TCTGATCATC TTGTGCAAGC 1200 AACTCACAAG CAGAGGCCCT GTGCAGTCAG GAGAAATCTA TACCTTTCCC CTTGGACATC 1260
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