Tag | Content |
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EnhancerAtlas ID | HS133-23190 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr3:159846800-159848720 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
PBX1 | MA0070.1 | chr3:159847287-159847299 | CTATCAATCAAA | + | 6.18 |
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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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| Number: 1 | ID | Chromosome | Start | End |
GH03I160128 | chr3 | 159846639 | 159849025 |
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Enhancer Sequence | CTCCCGGGTT CAAGCGATTC TCCTGCCTCA GCCTCCTGAG TAGCTGTGAT TACAGGCACA 60 TGCCATCACA CCCAGCTAAT TTTTGTATTT CTCGTAGGGA CGGAGTTTCA CCATGTTGGC 120 CAGGTTAGTC TCGAACTCCT GACCTCAGGT GATCTACCCA CCTCGACCTC CCAAAGTACT 180 AGGATTACAG GCATGAGCCA CTGTGCTGGC CGAAAGTCCT TGGACTTTCT TATCTCAAAC 240 ATGTAAGCAT GGACCTCCTC TCTTTCAGGT TTTTCTGGCC CTATTTTGTC TGGGTCTGAC 300 AAACGTGATT TCATCTTGCT ATCTGCAAAT TTCACATCAT GATCCTAGTA ATCATTATAT 360 AAGAATTTGG GTTACCAGGT TATGTAGGAA AGTAAATACG TTATTAAAAT GCCCTCCTGA 420 GCTGTCCATT TATTTAAATC ATCCCCCATG AAACATCCCT GCCCAAACAC ACTAGTACCC 480 ATGCCAGCTA TCAATCAAAG ATCTGGGGTC AGTCTCTCAT CGGCTGTCAG ATACTGTAAA 540 TGTACCTGCC ACTTTCAGAT GATATTCACG ACTACAAAGA CTACTATGCA ATCAATTGCA 600 AAGTGAAATT GCAAGTCTCA TAAAAGATGT GGTTCATGAA GCAATGAGTG TGACATTGGA 660 GAATTATTTG AATCACATAC AAAGCCGCAA CAGACAGGAA GAAATAATTA GCAACAGGGG 720 AAGAGGAAAC TGACCAGACA GATTTGGCAG ACATCACAGT TGACTCATTC AGTATCTCCC 780 AACTTTGCTT GCCTTACTCT GCTTTAAAGG CTGGAAAAGT TGAAATAGCC TCTTTCCCTG 840 TCTTCCCTGC AGCCAGCAGG AACTAGATTG CTCAGATTCA AATCTGGCTT TTTCTCTTAC 900 GAGCTGTGTG ACCTTGAGCA AGTCATTTAA CCTCTCTTTA CCTCAGTTTT CTCATCTGTA 960 AAATGTAACT GCCTCATAGA GTTGTTCTGA GGATTAGATG AGTTAGTATA TGTAGAGCTC 1020 TAAGAACAGT TCCTGGCACA CAGCAAGTCC ACAGTAATTG TGACCAGGAG TCTAACAGAT 1080 GTAGAAGTCG GGTTGCACAC GTGCGCAACT CTTGTGGTGG AAGTGAGGAG CCATGGTTGA 1140 CATTCCCTCA GACTGCATAT TTTGGAGGAG GGCTAGTTCC CTGTAGGACA CTCTGGATGC 1200 TGGGTGGGCC AAAACCTAGA GGTCCAAAAG TTCTCTGAGA TCACCAGGGA CAGCTCAGGG 1260 TGATTGTCAT ATGTCATGTC TTTAGTCACC AGTGGCCCAA GGAGAAGATA CATAACTGTT 1320 GAATTCCAGA GTCATCACCA CTGCTATCTT GCAAGGCTAG TTCACATCCA ACCAAGTTTG 1380 GAAGTGTTTT TCTTCCTACC CTGATATTCC CCTTACATTT TCTTATGCTT ACTTTTCTCA 1440 GCCCTCTATC TATTCACATA CAATTATGAT AAACACTCCT TTTCCCCTCC ATAATGTTAA 1500 TCTGTCACTA TTTGGAATGC ATAATCTTTT TTTTTTTTTT TTGTCAGAGT CTCACTCTAT 1560 CTTCCAGGCT AGAGTGCAGT GGTGTGATCT CGGATCACTG CAACCTCCAC CTCCTGGGTT 1620 CAAGCAATTC TCCTGCCTCA GCTCCCCGAG TAGCTGGGAC TACAGGCGCG TGCCACCACA 1680 CCCGGCTAAT TTTTTATAAT TTTAGTAGAG ATGGGGTTTC ACCATAGTGA CCAGGCTGGT 1740 CTCAAACTCC TGACCTCGTG ATCTGCCCGC CTCGGCTTCC CAAAGTGCTG GGATTACAGG 1800 CGTGAGCCAC TGCAGCTGGC CCGGAATGCA GAATCTCGCC AACACTTGGT TGACAATACA 1860 TTATAATTAT CAAAATAATT AAGCTCCATT TCAGTCCTAT TTATCAAGTT TCTACTATTC 1920
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