Tag | Content |
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EnhancerAtlas ID | HS133-19569 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr20:55947210-55948490 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myog | MA0500.1 | chr20:55947739-55947750 | CAGCAGCTGTC | - | 6.14 | Tcf12 | MA0521.1 | chr20:55947739-55947750 | CAGCAGCTGTC | - | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_53875 | chr20:55946877-55948029 | Spleen |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr20 | 55947244 | 55947298 | chr20 | 55947369 | 55947532 |
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| Number: 1 | ID | Chromosome | Start | End |
GH20I057371 | chr20 | 55946878 | 55948029 |
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Enhancer Sequence | TCATGTTCAC TCTTCTTACC ACAGTAAAAT CAGCACTTAG ACCTTGGCCC TGGTTCAAGG 60 CGTCCTCCGG AGCTGAGGCA GGGGCTCTTG TAAGCGGCAC CACTGGCCTT GCCGGACCCC 120 AGCCTAAGCC CTTCCCTGCC TCCCCATTTC CTTTTGGTTG AATCCAAAAA AAACCTGGTC 180 CCATCTGGCT TCACTTCCTG CCACCCGGTG CTAGCGCCCT GGCCTCTCCG TTGTTGAGAA 240 CTGATTGCCA TCGGCCTTTG CACAGGGCCA GTGCATGTGG CTCTTGGTGC AAGTGACACC 300 CCTGGCATTG TGCAGTTCCT GGTGTGCCGC ACAGTAGACC CTGTGCTGAT GACCAGCCAT 360 GGCCTTTTCT GTCATCTAAG AACTTACAGA TGTTTGTCAG TTTGCTTTAC TTTTTTTCTT 420 CGTACTCACA AAAGTAATGG TCTGGCAGTT TTTAAAAAGG CAGGGGAGCA AACAGTACAG 480 GAATGAAAGA GGAGGCCGTT TTCCTTCGTA CTTAGGAAAC GTGCATCACC AGCAGCTGTC 540 ACGATGCCAG AGGCTGCTTC TCCCTTCGTC TTGCCTGGCC CCTGCCTGGG TCCTGCCAGG 600 CTTCCCCTGA ACTCACACGG AAGCTCAGAT GACCAGCTTA GGCAGGGTGG ATGGCCCTCC 660 AAGCTTTGGC CAGGTTGCCA CGACTGGAAG GAGGAAGTGG TAACTCCAAA GTTGGCTTCT 720 CCTCGGGGTG GTCGGCTTTT CTGCCCAGGA GGCTGGGTAG TGGAATTTCT GGGTTCTTCT 780 GTAGAATAGA GACCTGCCCT TGGGCCCTCA CACTCAACAC TGGGCGAAGT GCAGCGTGTT 840 GCTTGTCTGT AGCATGGCCA CTGCACCCAC CGTCCCCTTC ACCCTGTTAC CCTGTGAGAC 900 GGGTGCGGCA GAGCCTGCAT CCCTCCTCCA GCTGGGGAGG CAGAAGCGCA GAAGCTTCGG 960 GTGACCTCCT GAGGGGTGTC TGCCTAGCCA GGGACGTCTC CATTCCCCAC AGGCAGGGCC 1020 GCTGTCTGCC TCGCAGCCCA TGGGGCTCTG CTGGCGTGAA CGCGGCCTTG CAGGGTGGCA 1080 GAGGGAGAGC GAGCAGCGGG GGCGGGGGAG GAGCACAGGG TGTGCAGTTG GGTCATAAAC 1140 TCACTGCTTA GATGGAGTTA CTAAGGAGTT AGAAAGCAAT GCTTACTGCT GTATCATATT 1200 TGAGTGATTT TTTCTGGTTC TTCTAAAACC TAAACATGGG GTAAAAATGA CTTACCTTCA 1260 CGTTAGTCAT GAAATCTTAT 1280
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