| Tag | Content |
|---|
EnhancerAtlas ID | HS183-08799 |
Organism | Homo sapiens |
Tissue/cell | T47D-MTVL |
Coordinate | chr7:5269360-5270460 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| BHLHE41 | MA0636.1 | chr7:5269754-5269764 | GTCACGTGAC | + | 6.02 | | BHLHE41 | MA0636.1 | chr7:5269754-5269764 | GTCACGTGAC | - | 6.02 | | IRF1 | MA0050.2 | chr7:5269544-5269565 | ATTCAGTTTCGTTTCCTTTTT | + | 6.03 | | MITF | MA0620.2 | chr7:5269750-5269768 | TGGGGTCACGTGACTTGG | + | 7.07 | | MITF | MA0620.2 | chr7:5269750-5269768 | TGGGGTCACGTGACTTGG | - | 7.07 | | USF1 | MA0093.2 | chr7:5269753-5269764 | GGTCACGTGAC | - | 6.14 | | USF2 | MA0526.2 | chr7:5269752-5269768 | GGGTCACGTGACTTGG | - | 6.48 | | USF2 | MA0526.2 | chr7:5269750-5269766 | TGGGGTCACGTGACTT | + | 6.51 |
|
| | 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 |
| GH07I005229 | chr7 | 5269129 | 5272910 |
|
Enhancer Sequence | CGAGACTTGG TAAGGGGCGT GACGCAAACC TGGAAGGTAA TTAGCCCCAC AGCCCCGAGT 60
GCTACTGCCT TCTGCTGGCT CCGGAGCCAC CCCACCAGCT CCTCACTGGG AAAGATGGGG 120
ACTGGTTCTG AGAACATAAG CGAGGTTGGT AAATGGGTGT TCCCAAGGCC TCTCTCAAGG 180
CTGAATTCAG TTTCGTTTCC TTTTTTTTTT TTTTTTTTAA AGGAGAGATG GGGTTTCCCT 240
ATGTTGCCCA GGGTGGTCTC AAACTCCTCC TGGGCTCAAG TGATTCTCCC GCCTCAGCCT 300
CCCACAGTGC TGGGATTATA GGCATGAGCC ACCGTACCAG GCTCATTTTC TCCGTTTTTA 360
AAGAAAATGT CATCCTGGCT CAGGTGACTC TGGGGTCACG TGACTTGGGC CCAGACTGGC 420
CACCTCTCAG CCAAGATACC ACCCTGAAAA GTACTGCCAA GGGTTTTGCC TCAGTCTTTT 480
CCCTCCCACC TTTTTCGTCC TTCAGCAAAT CTGCATCGAG TACTGCCTTC ATGCTGGGCC 540
TGTGAAGTGC AGAAGCTGTA GGGGAATGAG GCCAATGGGC TCCCCTCCGG CGGCAGCACT 600
AAGACCCATG CATGAGATCC TCCAGCCACA GCCTTGGCTA TGTGAGCCAC CTTCTTAAAA 660
AAGCCAACTC GCACTCCAGT GGGAGAGCCT GTGGTTTTGC ACCCACGCAG GGCTGTGCCT 720
GCTCGCTGCC ACTCCCATCT GTGAACCGGC ACTTCCAGTT CATGAGCCCA CCCTGAGAGT 780
CTCCTAGTGT CATTTTTTTT CCTGGTGTTA TTTTTGAGCT CTTAACCAGC TTGAGAGAGT 840
TTGTGGCCCG TCCATGAGGG AGCCTCTGTT TACTGTGCAG GCATCATTTT GACATTTATG 900
AATGTCAGAG AACAAATGAC TTCATCTCGA GCTGCCTAAG GCTGCAAAGA GTTCATTAGA 960
AAGCAATCAG AATTCAGAAC GTCTTAGTAC AGGCTTCAGT TTATAAATAT ACACCAGTGT 1020
TTCCAAAACA CAGTCCTCAG TGTGTGTCAT GGGGTCTGTG GTGTGTCCCC AGCCTTTGAA 1080
GGGTGACTTC GTCGTCTCTT 1100
|
