| Tag | Content |
|---|
EnhancerAtlas ID | HS133-19009 | Organism | Homo sapiens | Tissue/cell | melanoma | Coordinate | chr20:36539860-36541310 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2C2 | MA0504.1 | chr20:36540996-36541011 | TGCCCTCTGCCCTGT | - | 6.02 |
| | | 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 |
| GH20I037912 | chr20 | 36540421 | 36540570 |
| Enhancer Sequence | CACAGCGGGC GGCTAATAAA GATCCGTCAC ACGGCAATTT AGTGTGTGCT GGCACAAGGG 60
CCCAGGTGGG TGGAGCCCCC AACGCCGAGG ATGCCCTGGC CCTACCCAGG GGTCATGGCA 120
GGGATGGGGC CTTCTCTGTC CCCTGTGTTG AGGCGTGGGG GACAGTGGCT CCTCGGTGAC 180
TTCACTTCAG CTCTTAAAGT GCCAGGATGG GGAGAGGGGC TGGGGTAATG CTGTTTTTTG 240
TCTACTATAC TCCCCTCTCC CCCACCCTGT GCCTGCCTTG CTGGGTGACT TGGCATGTCC 300
CTGCCCCTCT CTGGGCCTCA GTTTCCCCAC TGAACAATGG TGAGTTTGCT TGAGCTCCAA 360
GCCTGTAGAA TTCTTCCATC TGTATACTTA GAAACCACAT CTTTTGTCCT GCAGCCAGCA 420
TGTATGTGCG TGTATGTGTG TGTGTGTGTG CATGTGTGTA TGTGTGCGGG TGAGGATGGA 480
GCTGGTGGGA GTGGTAGGAT TCCATCAGCA CCTTAACTCT CAGTGGCCTG CAGGCATCTG 540
CGGACCAAAC AGCAGCCAGC GTTCATCAAG AACTCTGTGT TTTCATCACT TCCCCTGCCT 600
CCTCCCATTT ACTCCCCACC ATGCTAGGAG GCGGGCCCTC CCATTTTACA GAGGAGGACA 660
CTAAGGGGCG TGGTGCGACT TGCCTGAGGA CACACAGATG CTGAACAGCA AAGCCGGGCT 720
TGAGCCCAGC TTGTGGGACG ACAGAGCCAG AGTTCGTAGC CTGCGCATCT GTCTGCTCCT 780
GGCTGCCAAG CTGTGTGTGT GGGCAGGTGC TTTGTTCTGG AGCAGCGCTC CTGGCTTGGT 840
CAGATTCTCA CAGGGGTCAG TGATGCCAAA ATGCTGAGAA TGCCCTGTTC TGGCTACAAG 900
CACATGGCTC CAAAAGTCTA GGCTCTGCGT CTGGGTCCAG CACTGTTAGT GGGAAGCAGT 960
GGGGCTCTGG GGGCATGTGT GAGACCCTGT GTGTTCCTGC CTGGGGGTTC TGGTGGATGG 1020
AGCGGTGTTT CTGTCTGACT GTGTGGGTGC GGGCTGTGTC TGGGGGGTGA CTGTGTGTGG 1080
TTGAAGGGGC AGTGCAGGCT GAGAGGGAGC CTGGGGGCAG GTCAGGGCTG GGCTGGTGCC 1140
CTCTGCCCTG TGCCTGTTTG CCTCAATACC AGCCTTCCCT GCCACCTGCA CACTGGTGCC 1200
CTTGGAGGTG AGGCTATGGG AGCATCTGGA AGGTTAGAGC AGGAGTCAGA GCCGGGAGAG 1260
GGGGCCTTTC TCCAGCAAGC TACCAGCGAG CAGGGCAGCA GTGCCCACCC GTACCTGGGA 1320
AGTGCCCTCC ACCGGCCCCT TACTCTCTGG ATCTCTCTCT CTCCCTGCCC TACTGCTCTC 1380
TGGGTCTCTC TCTTTCTCTC TCCCCCTCTC TCTCTGGGTC TCTCTGATCT TTATCTCTTT 1440
TCCTCTCTAT 1450
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