| Tag | Content |
|---|
EnhancerAtlas ID | HS091-10607 | Organism | Homo sapiens | Tissue/cell | HepG2 | Coordinate | chr12:99092150-99093180 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NKX2-3 | MA0672.1 | chr12:99092588-99092598 | TTCAAGTGGT | - | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr12 | 99092368 | 99092958 | | chr12 | 99092996 | 99093059 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH12I098698 | chr12 | 99092466 | 99093370 |
| Enhancer Sequence | AAACTGATTT CTCATATATT CTGGATAATG TAACTGAAGG TTCAGGCTTT TATGTTTATT 60
TATTTATTTT TCTCTTTAGT ATCAGGGAAG GCTGTTTTAG CACCTGCTGT CTCTTTTGCA 120
TTACCCAGAT TACCTGCAGT TGTTGCAAGT AGAAAAGTTT TGGTTTTGGC CATGTTTCTT 180
AGTATATATA ATACTTCTTT TTACTCGAGA GATTTGAAAA TGTACCTGGC CAGAAAAATT 240
AGGTTTTACC TGGGAGTTGT GCTTTGGAAG CTGACTTAAA GCCTGAGCAG CAGCTTTCTC 300
CCCCAACCCC CATCCTTCTC CGTGGCCAAC CTTTGGTTTG GGCATGGGCA GTCATTATCA 360
CTCTGTGAGG CTGAGACACT GCTCATGGCC CAGAGGAGTG AAGGTGGATC TTCTTGAAGG 420
CCTTTGTCTT TTGTGCTATT CAAGTGGTCC TACTAGTGAG CAAAGTTTAC AGTATTTTGT 480
ATCTCATTCC TCAGGATCCA GTTAGTTTTG TAGCCCTATC TGGCCCTGCC AAGCACACAA 540
AGAGTCTTGC TTGTCCCTGT TTTCAGAGAC TTCCTTATGT CTCTGGATGC TCTGCTAGGT 600
CACGACCTAA CTTGGACTGG GTCCTGTGTA GTCTTCCTGC TGTGCATGTG GTAGGTTCGT 660
GAAACACACT TCATTCCTGG CACAGCAGAG GGCAGCAGTG GCAAGTCGTG AGTCTCTTCA 720
TCTTACCACC TTTCTTCCAC TTGTGTCCTT ACTGTCAACA TGTAATTTTT AGCTTCCACA 780
CCATGCAAGA CTCTTAACTT TTTATTTAAT TTTATGTTCT GCATTTTGGG CAGTGCTTCT 840
AATTTTTTCT TTTTAAGAAC GTAATAATGA AACTGGAGAT CTTAATTTAA AAGCCTTACA 900
AAAAGTCATG CATAGGTAAA AATAATTCAT CAAGTGAAGT GAATAAGTTT ATGTGGCATT 960
TAATTTAGGA AAAATTCTAG AAGTGTGATT ATAGAGTAAA ACAAACTTTT TCTTTTTTAT 1020
TACTTTAATT 1030
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