| Tag | Content |
|---|
EnhancerAtlas ID | HS012-18784 | Organism | Homo sapiens | Tissue/cell | Caco-2 | Coordinate | chr3:184362830-184363890 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr3:184363275-184363287 | AATTGTTTGTTT | + | 6.22 |
| | | 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 |
| GH03I184645 | chr3 | 184362947 | 184364010 |
| Enhancer Sequence | GGAGGCAGGA GAATCACTTG AACCTGGGAG TCGGAGGTTG CAGTGAGTCA AGATCGTGCC 60
ACTGCACTCC AGCCTGGGGG ATAGAGCGAG ACTATGTCTC AAAAATAAAA ATAAATTTCT 120
GGGTTTTCTT TTAACTGACC AACACTATAT CCATTTTAAA GATAGACTGA GCACCCTGGA 180
GAAACTTGAC CCTGTGTTGC TCCCATCTCA GCCCCCAACT ACCCATCTCT CCCTCCTGTC 240
CATTAGCAAA GGAGAGCCCA GGGCTTCCAC CAGGCCTTCC ACCTGCCCCA ACCTGCCTGC 300
TCTGAACATT TTTAAGCATT CTTCAGGCAC CCGCTGCAAG GGCACCTCTT CTGGGGAAAT 360
ACCCCTGATC CCCAACACAG CTGGAGTCTC CTGCTCCAGG CTTCTGGGCT CACACTTCCT 420
GGCAGCTCTT ATCAGGCTGC TTGGTAATTG TTTGTTTTTC CAACACTGTT TCACAATTAC 480
TGTGCAATTT ACAAACTTGA CAACTCAGTG TGATCCAGCT ACTGCAGAGG TGCCACCCAG 540
GTGCTGATTC CTGCAGGGCC AGCCCTTCCA AGGAAGAAAG CACCACCCCC AGCCCTTACC 600
TGTGCCCACC CCCACCCCAG GGCCTACACC AGAACCTGGC TGGAGGAGGC CCTTGGTAAA 660
TGTTTATCGA CTGAAGGAAC ACGTGAATGA GGGATGGAGT GGAGGCTCTG GGAACAAGGC 720
AGAGGGGAAG AGATGCTTCT TGTTAACATC TCTTCATAAA AGCCAGTGAG TTCCTACATC 780
CAGCTGGTGT CTGAATTGGG GCCAATCATA AAACCAGGAG GCCCCTGAGG CTGAGGGCAG 840
CTGGCTGGCC AGTGGGCTTT ATAAGGCGGT TTTATGGACT CAGCTGAGAT GTGGTGATGA 900
GAAGCCAAAC TTTAAACATC CTCTTAAAGT TCGTTTTCAC TCCCCTGGGG CTTCTAGCTG 960
AACGAGATTG AGGAGAAGGC CTTTTGAGGC ACCAGTGGAG GGATGATGAG ATAGCATCAT 1020
CCACATGGAC CAAAAGGAAG TAAGCGGGAC TTGCAGCAGA 1060
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