| Tag | Content |
|---|
EnhancerAtlas ID | HS012-17416 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr20:49291720-49293180 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myog | MA0500.1 | chr20:49292346-49292357 | CAGCAGCTGTC | - | 6.14 | | Tcf12 | MA0521.1 | chr20:49292346-49292357 | CAGCAGCTGTC | - | 6.02 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_47109 | chr20:49267408-49294182 | Panc1 |
|
| | 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 |
| GH20I050672 | chr20 | 49289153 | 49294021 |
|
Enhancer Sequence | GATTCTTCCT TAGAGTCTTC AGAGGGAAAG TGGCCCTGCT GACACCCTGA TTTCAAACTT 60
CTAGCATCCA GAACTGTGAA AGAACGAGTT TCTGTTGTTT GAAGCCACCT AGTTGGAGGT 120
GCTTCATTAC AGCAGTCCTA GGAAGCTAAT ACAGGTGGTT ACCATGCACT AGGTTCTCTG 180
CATTATAAAT GCATCATATG TGTGAATTCA CCTAAATCCT CACAACAACT GTAAGAGGTT 240
ACTATACCAT GTTACAGAGA GAGTGATCAA GACTCAGAGA AGTTAAGGGA CTCATAGCTG 300
GATCTAGATT TGAATTTGGT CTATCTGGTC TAAAGCCCAC TTTTAAGGAC CAACTGTGTA 360
TGCCAAGTGC TAGAGCCACT TCCTTGCTCA GTCCTCACCG ACCACACTGT GCTATCTTTA 420
TTCACATTTT GCAGTTGAGG AAACAGGTTC AGGCAGGTCT GTCCAAGGCC ACCCTATTTA 480
GGGTCTGACA AAGCCAGGTT CATCTGACTC CAATGCCAAC GCCCATGCTG TTGACCAGAC 540
CATCCCTGCC AACTTCCCAA TATGAATGCT TTGAGTGGCT CTCGGCCCCC GGGCTGTGGA 600
ACACCAGCAC ACCAGTGCCT GGAGGGCAGC AGCTGTCCAG CAAATGTCTG CTCATTCATT 660
TGTTCACGCA TTCAGGGCAA GTCGAACGGC AGACGGGGCA GGAGATCCAG GGCCAGCATC 720
GATGGTGCAG GGAGCCCTCT GGCCCCTTAA ATATCCTCAG ACAATCCCAG AAATCATTCC 780
TGGGTCTACC TTATGTGGGT TTTCTAGAAT AGCTACTGCT GAACTGTAGG GTAGTGAGGG 840
AGAGACACAA ATACAGGCAA AACCACACAA CAGCGAAGAT TCCATAAGGG CAGGAGTGTT 900
TTTCCACCAG GAAACAAGAA CCAGTTCATC TGAGTTCCTT CGCCTTTTGT CCCAAGACAC 960
AAAAATGTCA AAAATGTGCA AGGGCTCTGG CCACAGATGG ATACTGTGTC TCACCCCGAC 1020
GGGCTGCTTC CTGCATGGGG CTGAAGGTCA GGGTGAAGGT TGCTGCCCTG AGAGTCAGGG 1080
GAAGTTGGTC TGCCTCCTGC TGTGTCACGT ACTTGCCATG GTGTGTGGGA TGAGGCCCAT 1140
CATCTCCCAG AATTAAGCTG TAGCTGACTA TAAAACCACA GGTGAGGGCT GGGTGTGGGG 1200
GCTCATGCCT GTAATCCCAG AATTTTGGGA TGCTAAGGCA GGAGGTTCGC TGGAGCCCAA 1260
GAGTTCAAGA CCATCCTGGG CAACATAGAG AGACCCCGTC TCTACTAAAA ATACAAAAAT 1320
TAGCCAGACA TGGTGGTGCA TGCCTGTGGT CCCAGCTACT CTGGAGGCTG AGGTAGGAGG 1380
ATCACTTGAG CCCAGGAGGT CAAGGCTGCA GTGAGCCGTG ATCATGCCAC TGTACTCCAG 1440
CTGGGGCCAC AGAGCAATAC 1460
|
