Tag | Content |
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EnhancerAtlas ID | HS133-10892 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr16:2983980-2985920 |
Target genes | Number: 33 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXC1 | MA0032.2 | chr16:2984369-2984380 | ATATTTACTTA | - | 6.14 | ZIC1 | MA0696.1 | chr16:2984488-2984502 | GGCCCCCCGCAGTG | + | 6.24 | ZIC3 | MA0697.1 | chr16:2984488-2984503 | GGCCCCCCGCAGTGC | + | 6.36 | ZIC4 | MA0751.1 | chr16:2984488-2984503 | GGCCCCCCGCAGTGC | + | 6.86 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr16 | 2984466 | 2984517 | chr16 | 2984572 | 2984890 | chr16 | 2985310 | 2985417 |
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| Number: 1 | ID | Chromosome | Start | End |
GH16I002934 | chr16 | 2984621 | 2984770 |
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Enhancer Sequence | GTACCTGGGG GTGGGCTGGG AGCTGGGCCC CAGGAAGCAG GCAGGAGCCC CACACTGCCT 60 TTCCCTCTCC ATGCTGCGGC TCCCCCTGGC AAACGTCCTC TTCCCTTCTT TGAACATCCT 120 AGAAGGAACT ATGGCCCTGG CCTCCTACTC CTTGGCCCCC CTGATGCCGC TTTCAATGGG 180 TCTCACCTTC CTGCTCAGCC CAGCCTCCCC CTTCCAGCCT GACCTGCCCC ACAGTAGCAG 240 CAGCAGGGAT AGACCTCCCT GCCCTCCTCT TCCTCCGTTT GTCTTAAGAG TTCATAGTAG 300 TAATAGAGGG TGTTGACTGC ACATGGTCAG TCTCGTTGCT ATGGTGGAAG GCTGTCTTAA 360 CGTCTGAGTG GTTAAGGATT GAGGAGGTGA TATTTACTTA CATGCAGCCG GTTTCTCCTC 420 TCGGCCCGCT GTTCCATAGA CACCCATAAT GTCCTGAAAC GCTGGCCCGA GGAGGGTCCC 480 GGCTGTCTCC ATCTTTATCC ACACGGTCGG CCCCCCGCAG TGCCTGGTGT TTTGACTTCA 540 CAACCACAGT TGCGTAAATG TCCCCATAGC GTCTGGCTGA GGAGCCATTT CATCGTGGCC 600 TCCTCCACTC ACCTGCTCTT CCTTCACGCC CCAAGGCGCT GGCCTCTCTT TCCAGTGGCT 660 CTTCCGGATC CTGCAGCTTT TGGGTCATGT GAGTTGCCTC ATGGCCCTAA AGTTCTCTCG 720 GACTTGAGAG CTGTGATTGT CTTTCTCTTT TTGTTCCATC TCCAGAGAGA CAGTGCTGCG 780 AGGTCCCCGC CTCGTCCTCA CCCCCGCTCC TGACCCCACA AGTAACTAAG CAATTGTTTC 840 TTAGGGTCTT GGCTGCCCTA TTTCCTAAAA TGTGCCTCCA CTACTATTAA TTGGTTTTTC 900 CATTTCCTTG TCAGCTACTC AGTGCACTTC TTGCACAGGC TTTTTTTTTT TTTTTTTTCT 960 TTGAGACGGA GTCTTGCTTT ATCACCCAGG CTGGTGTGCA GTGGCGTGAT CTTGGCTCAC 1020 TGCAACCTCC GCCTCCCGGG TTCAAGCAAT TCTCCTGCCT CAGCCTCCTG AGTAGCTGGG 1080 ATTACAGGCG CCTGCCACCT CGCCCAGCTA TTTTTGTATA TTTAGCAGAG ACAGAGTTTT 1140 ACCATGTTGG CCAGGCTGGT CTCAAACTCC CAACCTCAGG TGATCTGCCT GCCTCGGCCT 1200 CCCAAAGTGC TGGGATTACA GGCGTGAGCC ACCATACCCG GCCACGTTTG GTTTCACTTT 1260 AGCCTAGAAA CCTGCTCGCG GCTGACTGGG GGGTGCTCTG TGGTCCCATC TTCCTAACAC 1320 AGCTCTGTCT TCTCTGTGGG GTGGCAGCTG CTGCGTTTGT TTGCCTGCTT TTGTGTGTCC 1380 AGGTCGACCC CACCTGGATC CGATCATCCA CAACCGCAGG TTGCTGGAAC CTCCCAGTGC 1440 AGCCTGGCCT GGGGGCAGAG GCCGGGCCCA GCTGTCCCTC GGGGTTCACT GTGCTGACTC 1500 CCTGCTTCTG GGCCTGCCTT TCTCTTTCTT GGTTTTCTTT ATAATTTTGT GGTTTGGAGA 1560 AGTCCTGCCT CCCGTCGTTT CCTGGGCCGG TCCCGGGAGG TAGCACGTTG AGGCCTTTCA 1620 TGTCTGAAAT GTCTGTCGCT TCCCTCCGCC GGAGGGGCAG CCTGGCCTCC GTGGTGTCAC 1680 AGGTGCAGAG CCTGCCCTTG AACGTCCCTG CCGCTTTTGC GTGACTGATC CTCTGTGTGC 1740 CGTCAGCTTT GCTTGAGGTT TTAGGGTCTT TGCTCCCTCC CAGCTGTACC TGGCTGTGCT 1800 GGGGGCCTTT TTAGGCTTTG GGCTTGTGTC CTTCATCGTG GGGTCATCCT CTCGTGCTCT 1860 TTGTTAACTT CCCCATCATC ATCCCTTTCT GTTGCTCCTG TTAATCAGAT GTTGATCCTC 1920 CCAGATGAGG GCGTCTTTTT 1940
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