| Tag | Content |
|---|
EnhancerAtlas ID | HS184-06764 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr11:121065300-121066590 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr11:121065615-121065634 | CAGCGCCCTCTAGTGTCTG | - | 6.46 | | Foxd3 | MA0041.1 | chr11:121065951-121065963 | AAATAAACAATC | - | 6.62 | | MEF2A | MA0052.3 | chr11:121065302-121065314 | GCTATTTTTAGA | - | 6.52 | | MEF2B | MA0660.1 | chr11:121065302-121065314 | GCTATTTTTAGA | - | 6.22 | | MEF2C | MA0497.1 | chr11:121065301-121065316 | AGCTATTTTTAGAAC | - | 7.09 |
|
| | 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 |
| GH11I121194 | chr11 | 121065439 | 121065909 |
|
Enhancer Sequence | TAGCTATTTT TAGAACCATT TGACATTTAG TGGGAGCTTG AAATCTAATA AAATTTCTTT 60
CAACCAGAGG AATTAAGTAA TTATCAAAAG ACAATCATGA AGGGCTAGGG TAATAAAAAA 120
TTACTTCTTT ACTAATTCTG AATTAATTTA CCATCCACCC TGTTTTGAAC TTCCCAGCCT 180
TTCTCCTAAA ACTCAGGGGA TCTCTACAGC TTGTACTTCA TTGCAATTTG GGCCTGTTTA 240
GAAGACCATG ATGATATTTT GCAGTGCCCC ATACGCTGAC ATCTGCAGCA CAGTCCAGTG 300
AAAAAGGAAA TGAAACAGCG CCCTCTAGTG TCTGCTGTTT ATTTTTGCAT GAAGCTCAAA 360
TGTGTATTGA ACCACACCAA TCGAATTATG ATTCCGGTCC CCCGCCCCAC TACCACCCTG 420
AAACCTTAGA CGCAGGACAT TATGAGAATA TAGCTTTAGA AAACACATCA AATGCCAAGG 480
ACGTTTTCTG GAGAACAGTA TGGGATTTAT TTTTATGCAT ACCGTACGCA TTACTCCAGG 540
AAATACCAGC ACTTGGCATC CCATGCAAAT TTTGCCCTTA ATATCCGTTT CTCTAATGTG 600
TTGACAAAAA TAGCTGTCAA GAAAAATTAA GTACCTCTTT AAGATGTTGA GAAATAAACA 660
ATCTGATCAA GAAAAACCCA TGCAATATTT AGTGGTCTTT TCCCCCCAGC AGAATGTGAA 720
ATACTTTCAC ATGCACCTAC AGCACAACGG CAATAACTCT GTTCTGACTA ATGGAAGGCT 780
CTGTTTGTGA TGGTTTAATT ATGTTTGCTG AAATACGACT CTCATATAAG ACAACATCTC 840
CATGGCAGAG GGACAGATCT CTGTGTCTAT AGATAGAAAT AAAATACAAA AGACTCATCA 900
TTCCATGAAG AACTCAGCAA TCAAATTCTA TTTGCTAAGG AAACAAATGG AGGAAGAATG 960
TTCACTGTAC ATTTCGTTGT GTGTTTCTGT TTGCATCTAG CCTCTAGGTT AGCTGTTGTT 1020
TTGTTCAGTA GCATAAGATA CTGATGGTGA AATAATTTTG AAATTAAGAT AGTCTCCTAT 1080
TGGACGAAAT AACAATCCCT TACACAAATG TAGCATCTTT CATAACAAAT GCTTTGCCAC 1140
TGTATTTAAT ATTGTTCAGT CCTAGATCAT GCTGCATTCT GACAGAGAAA TTAGAGGAAA 1200
AGTACTAAGT TGAAGTTATA TATATCCAAA AGTACTAACT AAAGAAGAAC ATAAACCTAC 1260
TCATATATGT ATGCTTTTAT GTGTAGGTTT 1290
|
