| Tag | Content |
|---|
EnhancerAtlas ID | HS133-26896 | Organism | Homo sapiens | Tissue/cell | melanoma | Coordinate | chr6:36783490-36785060 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP1 | MA0481.2 | chr6:36784401-36784413 | TCCTGTTTACTT | - | 6.07 | | Foxd3 | MA0041.1 | chr6:36784554-36784566 | GTTTGTTTGTTT | + | 6.32 | | Foxd3 | MA0041.1 | chr6:36784550-36784562 | GTATGTTTGTTT | + | 6.37 | | Foxo1 | MA0480.1 | chr6:36784401-36784412 | TCCTGTTTACT | + | 6.32 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CCGAGGAAGA TCATTCAGAA TATTTAGAGA TGAACCATCA ATTTCAGCTG CTGGTGAAAA 60
GTTTAACAGG CTAATTCTCC TCAAAAAAGA GACTGAGTGC TTTGGCAGGG ACATGTGGGT 120
GTGGTGGCTG GGGCCAATGA CTGCAGTGGT ATGGGGCGAT CTGCTGGACA CCCTAAGATT 180
CTGTGATTCC CATTTCTTTT CCAAGAGGCC CTCAGCCAAG ACAGCTGCCT GGTGAGGGAG 240
GGGCAGGGAT CTCCATACCC ACTTTTCAAA TGGGAAACCT AGAGGGGTTC CCTATCATGT 300
CCCTCTTCCC AGTGGAAGCA TTTCTGGGAC TCTTCCCACC TGGCCATCCT GCCTTAGTTA 360
GTCTACCCAC GAAGGTCTCT TAGCCCCATT TTATAGATTA GTAAGCTGAG ACTTGAGAAG 420
ATAAATAACT CACCTAGGTC ACACAGTCAG TAAATATCAG AGCTGGTCTG AAAACCCAGG 480
GTTTTGGACA TCAAGTTCAG GCCTCATCTG ACAAATGCAT TTGACTGGAC ATGCAGAAGG 540
CCCTGGCAGG ACTTGATGCA AACAGTGCTT GATTTTCTGG GCTAAAATTA CATCTTGAGT 600
CAATTTTCAT GAAATGTGGT GACAGATTTA GGTGCTGGGA AGATGGAGCT TTCTCAGAAG 660
GCATAAAAAT GACCCAAATG GTTAAAACCA GCTGAAAGCC GGCAGCCAGG GGCCACGAGA 720
GCAGATTTCA TCCCTCCCAG GATTGGCTCA TCTGCAGCCT CATGCAAACC CCACGTACAG 780
AGAAAGTGCT GTGCCTGCAC TTGACTTCCC CTGACCACAG GATTATTATT TCTCGGACAA 840
GATTCTGGTA ACAGAGAGGT GATTTGTTCC TGAAGGGCAA TGAACTAGAT GGAGGAGTGG 900
TGGGAACTGG TTCCTGTTTA CTTGCAAGGG CAGTCTTCTA TCCCAGAGGC GGTTCCATAG 960
AGACAATCTG GATTTTTCTT TAATTCTCCA TTCCTGATAC TTTCCTCTGT GGGTCGCACA 1020
GAGAATCGAG CAAGGAATTA CAGCCCCTCT CCCGTCCCCA GTATGTTTGT TTGTTTGCTT 1080
TCGAGACAGG GTCTCATTCT GTTGCCCAGG CTGGAGAGCA GTGGCACAAT CTAGGATCAC 1140
TGCAACCTCT GTCTCCTGGG TTCAAGCGAT TCTCCTGCCT CAGCCTCCCA AGTATCTGGG 1200
ACCACAGGTG TGGGTCACCA TGCCTGTCTA ATTTTTAGAT TTTCAGTAGG GACGGGTCTT 1260
GCCAAGTCGG CTAAGCTATC CCCAGTATGT TTAGATGCAT CTTCCTTTCT CCAGAAAAAG 1320
CTGTGTGAAG GCCGGGTGCA GTGGCTCACG CCTATAATCC CAGCACTTTG GGAGGCTGAG 1380
GCGGATGGAT CATCTGAAGT CAGGAGTTCA AGACCAGCCT GGCCAACATG GTGAAACCCT 1440
GTCTCTACTA AAAATACAAA ATTAGCTGGG CGTGGTGGTG CATGCCTGTA ATCCCAGCTA 1500
CTCGGGAGGC TGAGACAGGA ATATCATTTG AACCTGGGAG GCAGAGGTTG TAGTGAGCTG 1560
AGATCATGCC 1570
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