Tag | Content |
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EnhancerAtlas ID | HS012-11145 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr12:96271340-96271980 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEOX2 | MA0706.1 | chr12:96271644-96271654 | GTTAATTACT | - | 6.02 | NFE2L1 | MA0089.2 | chr12:96271601-96271616 | AGTGCTGAGTCACTG | - | 6.58 | Nfe2l2 | MA0150.2 | chr12:96271603-96271618 | TGCTGAGTCACTGTT | - | 7.11 |
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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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Enhancer Sequence | GAGCTGGTTG TGGGTCTAAA AGCTAACCTC ATCATTCATT CAACAAACAT TTATTGAGCA 60 CCAACTTTAA AGGGACCCTC AACTGAATGA AGAATAATAA GTCAATCCCT GCACTCAAGG 120 GGGTTTGCAT CTAGCTGAGA GATGAACTTG TCAATAAATA AGTGTACTAG CACATATCAC 180 AGCTGTTTTG ATAATGAGTC TATGCAGGCC TGAAGAGGCA AAAATCTAGT ACAGGCTCAG 240 TGTTGGGAAA ATTTTCTAGT CAGTGCTGAG TCACTGTTAA TTGTGTTGAT TCATGGCTTC 300 CTCTGTTAAT TACTCCTGGA ATTACCACCA AAATGATAAC ACACAGTGAA CTACTACATA 360 TGTCTAGGCT CTGAAGAAAT GTATTTCGAG GGGAAACTAT GGTCAATATC ATGCATTGCA 420 AAAGAGCAAC GTTTTAAGAG AACCCCAATG CCAATTTGAA TGCTTTCTGC CTATGTAAAT 480 TGGCTATTAC ATAATGGCAA GATAAATTCC AAGCTGGCTT TCCACTTCTG TCATCAATCT 540 AGGACTTGTG ATTTGCTTTA ACTCTCCTAT TCACATACTT AGGACACAGG GAATAAAAAT 600 TATAATCATG AGCCAAAATG AAATCACCAT AGGCAAAGAG 640
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