| Tag | Content |
|---|
EnhancerAtlas ID | HS012-11708 | Organism | Homo sapiens | Tissue/cell | Caco-2 | Coordinate | chr12:111825230-111826280 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr12:111825270-111825285 | TGAACTACTGACCTC | - | 6.07 | | RARA | MA0729.1 | chr12:111825267-111825285 | AACTGAACTACTGACCTC | - | 6.45 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GAGACAGGGT CTCACTATGT TGCCCAGGCT GGTCTCGAAC TGAACTACTG ACCTCAAGTG 60
ATCCACCCAC CTTGGCCTCT CAAAGTGCTG GAATTACAGG TGTGAGCCAC TGCAACTGGC 120
CAGATATGCC ACCTTTGGTT TATCCATCCA TCCATCCATT GAGGACCGCA GGGTGTCTCC 180
GTTTGGGCTA CTGTGAACAC CCAGGCATCT TTGTGGCTGG GAACAGGAGA GGTGTGGAGA 240
GCAGACAGTG AGTCAGAAGA ACTAAAAAGG GAAATTTGGG AACTAGAACT GGGCTTTGGC 300
CACCGAGATC AAGTCCTGAT TTTACCTCCA AACCGTGTCT TGAATCCATC ACTTCTCCAT 360
CTCTGCCACC ACTTCCCCAT CCCAGGCCAC CACTATCTCT CCCCAGGTCG GTTACTGCAG 420
CCTCCCTTCC GGCCTCCCTT CTGCCACTCC CAACTCCCTC ATCCCCAGGG TTCATTCTCC 480
ACTGAGCAGC CGAGGGATCC TCTTAGAACT TTCATGAAAT CAAGTCATGG CACCCTCTTG 540
CCCAAAGCCT TTCCATGGCT CCCCATGGCC TTGGGAGCAA GTCCAGACTC CATCCCATGG 600
GTGACAAGGC CCTCCTTATC CTGGCTGCTG GCTACCCCTC AAGCCTCTTC ACACATGGTT 660
TACTCTCCTC ACGCTTCGCT GCAGCTGCCT GGCCTCCCTC TCTTCCCAGA GTGCGCCAGG 720
CTCCAGGCCC TTGCATGTGC TGGTCCCCTT CCCAGGAGGC TTCCTCCTTC ACTCAGCCAC 780
CCCTCATCCT TTAAGTGTTC ACTCAGCCAT TGCCTCTTCC AGGAAGGTCT GTGACCCCAA 840
CCCTTCCCCT CCCGCTAAGT CAGAGGCCTT CGCTGCTTCC CATTAGCCAT TCTTTCAACC 900
AGTATTTACT GGGCACTGCT TTGTCCCAGG CACCAGGGAT AGAAGTTAAA AAGACAGGCA 960
ATGGCCAGGC ACAGTGGCTC ACACCTGTAA TCCCAGCACT TTGGGAGGCC AAAGCAGGCG 1020
GATCATTTGA GGTCAGAAGT TTGAGACCAG 1050
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