Tag | Content |
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EnhancerAtlas ID | HS133-00034 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:1407870-1409490 |
Target genes | Number: 43 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr5a2 | MA0505.1 | chr1:1409475-1409490 | TCTGGCCTTGACCTC | - | 6.59 | Zfx | MA0146.2 | chr1:1408827-1408841 | CCCGCCTCGGCCTC | + | 6.01 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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Enhancer Sequence | GTAACAAGGG AAGCGTATTT GAGAGTTACT TGATTCTAAC GAGACTAGCA GATTTGCACT 60 TCTTGTTGGA AGACGTTAGC ATTTGCACGG CGAGGTCTGT GAAGCCACAG GCCAGGCCGT 120 GCTGCTCAGC TTGAGTAAAC CCCTGACCCA AGGCCCTCAG GGTGTGAGCA CTGACTGCAC 180 CTTCCCTAAG CTCGGGTCTC TTCCCCCAGC CTTCCTTTCC CCTGTGGCTT TAACGATTTG 240 TAGCACGATG CAGTTCAAAT GGCTAGGAGT CTGGAACGTA GAAGGTGCTG AATTCATTGA 300 AAGAATACAG TGGTTCTCAA CTCTTGTTTA AGCCGGGGTT CTTTCTATTT ATTTATATAT 360 TGAGACACAG TATCGCCCTG TCGCCGAGGC TGGAGTGCAG TGGTGCGATT TCGGCTCCCT 420 GCAACCTCCG CCTCCGATTC TCCTGCCGCA GCCTCTCGAG TAGCTGGGAT TACAGCCGCG 480 CAGCACCACG CCCGGCTAAT TTTTTTTGTA TCTTTAGTAG AGACGGGTTT CACCATGTTG 540 GCCAGGGTGC TCTCCAACTC CTGACCTCGT GATCCGCCCG CCTTGTCCTC CTGAAGTGTT 600 GGGATTACAG GCCTGAGCCA CAGCGCCCAG ACAGAAGGGA TTCCTTTTTT TTTTTTTTTT 660 TTTTTTTTGA GATGAGTCTC GCTCTGTCGC CCAGGCTGGA GTGCAGTGAC GTGATCTCCA 720 CTCACTGCAA GCTCCGCCTC CCGTGTTCAC ACCATTCTCC TGCCTCAGCC TCCCGAATAG 780 CTGGGAGTAC AGGCGCCCGC CACCACGCCC GGCTAATTTT GTAGAGATGG GGTTTCACCG 840 TGTTAGCCAG GATGGTCTCG ATCTCCTGAC CTCGTGATTA ATTTTTTGTA TTTTTAGTAG 900 AGACGGGGTT TCACTGTATT AGCCAGGGTG GTCTCGATCT CCTGACCTCG TGGTCCACCC 960 GCCTCGGCCT CCCAAAGTGC TGGGATTACA GGCGTGAGCC ACCGCATGCC ACCTTTTTTT 1020 TTTTAAGATG ATGTCTTGCT CTTTGGCCAG GCTGGAGTGC AATGGCGCCA TCTTGTCTCA 1080 CTGCAAACCG CAACGCCCTG GTTCAAAGAA TTCTGCTGCC TCAGCCTCCC AAGTAGCTGG 1140 GATTACAGGC ACGCGCCACC ACGCCCAGCT AATTTTTGTA TTTTTAGTAG AGACGTGGTT 1200 TCACCACCTT GGCCAGGGTG GTCTTGACCA CCTGACCCCG TGATCCACCC GCCTCGACCT 1260 CCCAAAGTGA TGAGATTACA GTCCTGAGCC ACCGCACCCT GCCAGCAGGG GTTCCTTTTT 1320 AGAAAGAAGA TCATTTAGGG AATCCCTGGT GTGAAGCAGA TATAAACAGA GTTTCCCTGT 1380 TTAAGGAGGG ATGGCCTGGT GGTACTTGTG GTTCCATCCT GTGCCCTTCC CCGGGGTGCT 1440 GGGGAACATC CTGAGCTGAG GTTTCTGGCC CCGGCTGGGT CTCATAACCC CAGAGGGACA 1500 TTCAGGTTTG GGCCCAGGCC CAGGCTAACA TGGATAGTCC TAGCTGGGCA CCACCGACAG 1560 TGCGTGTTCT GTTTTGAAGA GATGGGGTCT TGCTTTGTCG CCCAGTCTGG CCTTGACCTC 1620
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