| Tag | Content |
|---|
EnhancerAtlas ID | HS133-03234 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:203475920-203476810 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GSC | MA0648.1 | chr1:203476104-203476114 | GCTAATCCCC | + | 6.02 | | Myod1 | MA0499.1 | chr1:203476089-203476102 | TGCAGCTGTCTCT | + | 6.36 | | Myog | MA0500.1 | chr1:203476088-203476099 | CTGCAGCTGTC | - | 6.62 | | Tcf12 | MA0521.1 | chr1:203476088-203476099 | CTGCAGCTGTC | - | 6.14 | | ZNF263 | MA0528.1 | chr1:203476772-203476793 | GGAGGAGGTCAAGGGGAAGAG | + | 6 | | ZNF263 | MA0528.1 | chr1:203476216-203476237 | GAAGGAGGAAGAGAGAGATGG | + | 7.07 | | ZNF263 | MA0528.1 | chr1:203476219-203476240 | GGAGGAAGAGAGAGATGGGGA | + | 7.09 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_00433 | chr1:203475229-203480110 | Adipose_Nuclei | | SE_40925 | chr1:203475444-203479251 | Left_Ventricle | | SE_54703 | chr1:203475335-203479326 | Stomach_Smooth_Muscle | | SE_55853 | chr1:203475518-203478980 | u87 |
|
| | 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 |
| GH01I203506 | chr1 | 203475417 | 203479129 |
|
Enhancer Sequence | GCTAGGATTC AATCCGGGGT CCATCCAGCC AGAGTCTGAA GTCCTGCTCT CTGCCACACT 60
CCAATGCAGA CACCATTTTC AAGTTCCAAT TAAAGGAGGC CAGCTCCAGA GAGTTTCTTT 120
CCCCAGGCCA TTGCTGCTCC GGGAGGGGTT CCCCAAGGGC CGCTGCCTCT GCAGCTGTCT 180
CTTGGCTAAT CCCCCATTTT TGGCTAGGGA AGCCCAAGGA ATAGAAAGAA TGCCCTTGTT 240
GTCTGTCTCC CTGAAGAAAT TCTAAACAGA GCATCTGTCC CTCTGCACCA GGGAGGGAAG 300
GAGGAAGAGA GAGATGGGGA GAGACAGAGA GAGAGAAACC CCACAGCTGT TCCTTCTCGA 360
TCTTGATGTG AACAGCTAGG CCTCCTGTTT CTCAGGTACC TAAAGGGGTT AGGGTTGGGC 420
AACTGGCAGG GAAGGCAGAG AGCACCTCTT TAGCCAGAGT GAGGCCCTCC TGTCTTGTAG 480
AATGGTAAAG ATGGAGAGAA TGACACAGAG CAGATGCAAG CCAGCCCTGA GAGAGTACAA 540
AGGAAGGGAG TGAGAGGAGG GGCTGTGGGG TCCAGCCAGG CACGGCAGCT AGCTTGAGGG 600
CCTCATGCCA GCCGGCAGTC TAGGTTTGCA TCACATCCAC CTCCTCCAAC ACCAGACTTT 660
CCTAACCTCA CTCATCCAGG TCCTTTGTGG CCCAGCAGCA ACTCATATTT GACCTTGGCA 720
AGGGCACTTG CTCTGGGCGG CACCCTGGTG ACTATTCTGC CAGCTCTGTG TGAAGGGGAG 780
TGCCTCCCTC CTCTGGGGCA CCCTGTGGCC TTCAGGAGGG TCTTGCCCTA ACCTGTCCTA 840
TGAGTATCAG CGGGAGGAGG TCAAGGGGAA GAGGCCAGGG CCCCTCCTCT 890
|
