| Tag | Content |
|---|
EnhancerAtlas ID | HS046-02497 |
Organism | Homo sapiens |
Tissue/cell | Fetal_muscle_leg |
Coordinate | chr1:180182640-180183360 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| BHLHE41 | MA0636.1 | chr1:180182706-180182716 | GTCACGTGAC | + | 6.02 | | BHLHE41 | MA0636.1 | chr1:180182706-180182716 | GTCACGTGAC | - | 6.02 | | MITF | MA0620.2 | chr1:180182702-180182720 | CAGGGTCACGTGACTAAT | + | 6.77 | | MITF | MA0620.2 | chr1:180182702-180182720 | CAGGGTCACGTGACTAAT | - | 6.77 | | USF1 | MA0093.2 | chr1:180182705-180182716 | GGTCACGTGAC | - | 6.14 | | USF2 | MA0526.2 | chr1:180182702-180182718 | CAGGGTCACGTGACTA | + | 6.66 |
|
| | 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 |
| GH01I180213 | chr1 | 180182536 | 180182962 |
|
Enhancer Sequence | AGAGGCAATC ATGCTCCCGC CAGTCCATCG GCTCCCCAGA TTTTCAGGCT CCAGCCGGGA 60
GTCAGGGTCA CGTGACTAAT TCTAGCCAAT GAGATGGAAG CGAGCGCCAC CTCCCGGAAA 120
GGAAATGATG CCCGTAACTT AGAGCGGGCT AAGGTGCTCA ACTCTCCAGT TTCCCTTCGT 180
CTGTCTTGGC CACAAAGGAA ACCACACATT CTAGATATAA AATGTTAGAG CCACCTGCCA 240
AACACTGTAC TTTTGTTATG CCACTGAGAT TTGAGGGTTA ATCTGATGCG GCATTGTATT 300
CTGGCCTATT TCAATTCTCT ACTGCTATCT GACAAACCAC CCCAAAATGT CTTAGCTTCA 360
AACAACACTC ATTTTCTTTG CTCATGACTC TGCAGTCTGG GCTAGTTTCA GCTGGGCAGC 420
TCTTCTGCAG GTCTTGCCAG GGTCATTAAT GTGGCTGCAT TCAGCTGGCG GGCAGGCTGA 480
AGGCTGGGCT TAGCTGAACT CACAAGACAG CTGGGCCTTT CTCTCCCCAC CCCCGTCTCT 540
CTCCCCACTC CCCGCCATAT AGTGTCTCCA CAAGGCCCAA GGTCTCTCTG GTAAAGTAGT 600
TGGACTTCTT GCACAGATGG GGGCTCAAAG CTCCCTAAAG TGCCATGCCA TCTTAAAACT 660
TAGTCCCAGA ATGGGCACAG TGTTACTTCT GGTACCTTCT GTCGGTTAAA GCAAATCACA 720
|
