| Tag | Content |
|---|
EnhancerAtlas ID | HS012-18451 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr3:133217870-133218530 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXC1 | MA0032.2 | chr3:133218218-133218229 | ATGTTTACATA | - | 6.32 | | Foxa2 | MA0047.2 | chr3:133218219-133218231 | TGTTTACATAGT | + | 6.22 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_31271 | chr3:133217053-133219475 | Fetal_Thymus | | SE_55369 | chr3:133217778-133218363 | Thymus | | SE_58435 | chr3:133156364-133225921 | Ly1 | | SE_62737 | chr3:133159951-133226397 | Tonsil |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr3 | 133218000 | 133218200 | | chr3 | 133218200 | 133218294 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH03I133499 | chr3 | 133218181 | 133218350 |
|
Enhancer Sequence | CTGACCTCAG GTGACCCACC TGCCTCGCCC TCCCAAAGTG CTGGGATTAC AGGCATGAGC 60
CACCGTGCCC GGCCTGTTCT ATGTGTTCTT ATAGTGCAAA GCATTTGTGG AAAACGTGCC 120
CTTGTTAGAG AGTTATGTTC TTCTGTACTG GTATCTTTGT ATGCCTTTTG CGTTCTAATC 180
ATTTATTCAA CATATATTTG AGTACCTACT ACTGTAAGAC AGTTTTTGGG CTCTGGTGAT 240
ACCACAAAAT AGAAAAAGTC CTCGTTTTCA TGGTGCTTAT ACTGTGTGTG TATGCTGGTG 300
TGTGTACATA GTGTGTGTGC TGTGGCAGGT ATTTGGGTTT GCTATAATAT GTTTACATAG 360
TTACTACACA TTTCCTGCCA TTTTACTGAC AGTTAAACTG GGCGGTGTTA TCTAAGTCTT 420
TCATCTCTCT AACAAAGTGA AGAGTGAATT CTCCTTGACA TTGTGTTCAC GGTATCTGGA 480
ACCAGTTTGA ATTCTATTCA GGGCTTCAGG TTAAATTCTA CATGTTGATT TTAACCCACT 540
TTTCTGTAGC CTGAGGACAG AACTGTTAAG ATTAAATTTA TGGACTTCAA CCTTACAAGT 600
GGTAATTCAG TTTGTTGTCA CAACAATGTT TTCTTTATAA ATTTAATTTT GATTACAAAC 660
|
