Tag | Content |
---|
EnhancerAtlas ID | HS184-31387 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr9:115899520-115900560 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MSC | MA0665.1 | chr9:115899571-115899581 | AACAGCTGTT | + | 6.02 | MSC | MA0665.1 | chr9:115899571-115899581 | AACAGCTGTT | - | 6.02 | MYF6 | MA0667.1 | chr9:115899571-115899581 | AACAGCTGTT | + | 6.02 | MYF6 | MA0667.1 | chr9:115899571-115899581 | AACAGCTGTT | - | 6.02 | NFAT5 | MA0606.1 | chr9:115900517-115900527 | AATGGAAAAT | - | 6.02 | NFATC1 | MA0624.1 | chr9:115900517-115900527 | AATGGAAAAT | - | 6.02 | NFATC3 | MA0625.1 | chr9:115900517-115900527 | AATGGAAAAT | - | 6.02 |
|
| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_03275 | chr9:115896818-115902916 | Brain_Angular_Gyrus | SE_07091 | chr9:115895468-115908997 | Brain_Hippocampus_Middle_150 |
|
| 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 |
GH09I113137 | chr9 | 115899694 | 115900661 |
|
Enhancer Sequence | CGACACCCTG TTTTTTTTTT TTTTTTTTAA AAAAAGCATG TTCTTTTACT AAACAGCTGT 60 TGAAATTTAA ATATTTACAC CCTATCTTTC ACAAAGCCCA TTTTTCTGAG AAGAAAAAGG 120 AAACTGGTAG AACTTCATTC TTCTTGGAAG AATTGTCAAG ATGATCTTTG CACAACCCTC 180 TGAGATCATT TCTCTCCTTT GCTCAGAGAT ATTTAATGCA GGAATTGCTG CTCTTTTCTT 240 TTTTGTGAAT CTGATTAAAA TTATGGATCC TCTCGAGAGA GAGAAGTGCC CCTGCACTGA 300 CGCACATAAA GTTTTGCATA TAACTTCTGT GGCTGTTTTA CACCCGGAAG TCTATGAATC 360 CAGGTTGCAA AAATCCAGAA AAGGAATGTT TGAACTCTGA AGCATCTCAG AAGCCAAGAT 420 TATGATCCTT GATTACACTG GCCAAGCCAG TCTAGACAGT GCCAGTAGCC TGCCCTGTCT 480 CTCAACTTCT GGTTCATCTC CAGGGAATGT TCAGTTCAGA CCTACCAAAG TTGACAGTCC 540 AGGCAAAATC TGCCTTTGAA TAGCAGTTCC CTCACCCTCG CTGCTCCTCG GACACTCTCA 600 GCTGCCCTCA ATGCATGGCA CTGGTGTGGG AATAGGTACA ATGGTGAAGC AGTCAGAGGC 660 AGGTGGAGAC CTTGTGGTGA TGAAATCAGA GCTGGCTTCC AGCTCTGCTC TGCCACCAGT 720 ACTGCTTGGT CCTTGGCAGG TCAGGTCCCT TGATCCCAGG CCAGCGCTCC TCCCTCCCTC 780 TGCTGTACCA CTGACCTAGG CTCATCTGCA GAGCCACGCC TGGAAAGTCA CACTTGAGGA 840 AACAGGCTGC CTCCTAGGAG AGATCCCAGC TTGAATAAAG GCTCCCACTA AATCCAAGAA 900 CCTCAGAGAA GGGCAACAGT GCAGGTGTGG AGCTCACACT GTGCTTTCTT TCATAGAGCA 960 TAACAGATGT TCTGTACTGT CCCTAAAAAG GGACAGGAAT GGAAAATGAC CCTCCTCAGC 1020 CTTTCAAAAG TTTGGGGCCA 1040
|