| Tag | Content |
|---|
EnhancerAtlas ID | HS184-20973 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr3:133217900-133218510 |
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 | TCCCAAAGTG CTGGGATTAC AGGCATGAGC CACCGTGCCC GGCCTGTTCT ATGTGTTCTT 60
ATAGTGCAAA GCATTTGTGG AAAACGTGCC CTTGTTAGAG AGTTATGTTC TTCTGTACTG 120
GTATCTTTGT ATGCCTTTTG CGTTCTAATC ATTTATTCAA CATATATTTG AGTACCTACT 180
ACTGTAAGAC AGTTTTTGGG CTCTGGTGAT ACCACAAAAT AGAAAAAGTC CTCGTTTTCA 240
TGGTGCTTAT ACTGTGTGTG TATGCTGGTG TGTGTACATA GTGTGTGTGC TGTGGCAGGT 300
ATTTGGGTTT GCTATAATAT GTTTACATAG TTACTACACA TTTCCTGCCA TTTTACTGAC 360
AGTTAAACTG GGCGGTGTTA TCTAAGTCTT TCATCTCTCT AACAAAGTGA AGAGTGAATT 420
CTCCTTGACA TTGTGTTCAC GGTATCTGGA ACCAGTTTGA ATTCTATTCA GGGCTTCAGG 480
TTAAATTCTA CATGTTGATT TTAACCCACT TTTCTGTAGC CTGAGGACAG AACTGTTAAG 540
ATTAAATTTA TGGACTTCAA CCTTACAAGT GGTAATTCAG TTTGTTGTCA CAACAATGTT 600
TTCTTTATAA 610
|
