Tag | Content |
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EnhancerAtlas ID | HS133-17345 | Organism | Homo sapiens | Tissue/cell | melanoma | Coordinate | chr2:100104960-100106270 | Target genes | | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HLF | MA0043.2 | chr2:100106054-100106066 | CATTACATAACC | + | 6.62 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AGATAAACGC AACACAGGAA AAGGCGCAAA TAGCCTAAGA ATTGAATGGA AGAGAGCCTT 60 GTATACTGGA GAATGATTCC TGGAAGAGGA ACTTTAGGTG AGCTCTTAAG TGTCCAGTAC 120 AGGAAGGCAG GGAACAATAC GCAGCACTGG TCCCTGCACG GGCAAACCCA AGAATATGTG 180 TGAAAGGTTG GTGGACAGAT AGATGGTTCC CACAGGCTGA TTTGCTACAT ACAGAACTCC 240 ATAGAAAGAA CCAAGGTTAT GGTTGGTCCT ACCCTACCTA AACAGGAAAT GGCTTATTCT 300 CGGAGACTAA AGTGCCAAGT CCGGAAAGAC CAGACAGATA CACAGAATTA CAGACTGTTA 360 CATAAAGTCC TTAATAGTTA CAAGCCCTTG TTGTGCTATG TGCTAGTCTG CATTATTTTC 420 ACCTAAATGA AACCATTTCT ACTTAGTACA TGGCGTGAGA AGACGTGGAG ATAAAGAGAA 480 TTAGCAGACG TATATTATCT GCAATTTATC TTACGGAGGA GTACATTAAG GAGTGTTATG 540 TGAGATTATT TCTTTACAAA CTGAGAATAG GTAGGAAGAG CAGCGAAACA CAGCGCGGCT 600 CGGTGCGCCC AGAGCGGCGT CACTGTAACA GTACAGAAGT GGGCAAGGGG CTCTCGGAAG 660 GACAGTTGGG GAACGGCGCC CAGCGTATTT AGCGAACGGA CAAGCAGCAA GGAAAAACAA 720 GGGAGCAACA ACCGCCTTCG GACATTCCGA CCGGTTCTGG GATGCACCGG GGACGTCGAA 780 GGCGGGGTGC GGAAAAACGC TGTGGCTGGA GTGCGGGTGG GAGCGGCGGC TCGACCGGGT 840 CGACATTCTA CAAACGCTTG TGGAACGAAC GCCCGAACGC GCGCGTGAAT GAATGGCGCG 900 GAACTGAATG GCCGGCCGAG GCGCCGGCGC AGGAGGAAGG AGTTTGCGGC GCGGTCTGAC 960 CGGGCCGGCG GGATGCGGCC GGGCGCGGAG GGAAGGGCCG CTGCGCCAGG GGTCGGCGCG 1020 GGGCGGCCCA TGGGGCTGGC GGCGGCGCGG GGCCGGCCGC GCCATGACGG AAGGGAAGGG 1080 GAGGGGAGGT CACACATTAC ATAACCCGGC GGCTGCGAGC GTCAGGGGAA GGCGCCGTGG 1140 ACAGCCCAGG CCGCGACAGG ACGGCCGCGG GCCGGGGCCG GGGCGACGCA CCCCTCCCCC 1200 GCGCCACCTC AGGCCGACCG CGCTCTGGCC GCTGCCGGGC GGGTCTGCGG CGCCTCCGGG 1260 CGACGCGTGT CCGATCCCGC CCCTCCCCCA CCCCGCCGCC GGCCCGGGGG 1310
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