Tag | Content |
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EnhancerAtlas ID | HS133-04285 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr10:29234980-29237390 |
Target genes | |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr10:29236854-29236866 | AAACAAACAAAC | - | 6.32 | IRF1 | MA0050.2 | chr10:29235867-29235888 | ATGGAGAAAGTAAAAGTAGAT | - | 6.28 | MEF2A | MA0052.3 | chr10:29235713-29235725 | GCTATTTTTAGA | - | 6.52 | MEF2B | MA0660.1 | chr10:29235713-29235725 | GCTATTTTTAGA | - | 6.22 |
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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 |
GH10I028946 | chr10 | 29235061 | 29236390 |
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Enhancer Sequence | GATTTTCTAT TTTATTTCTT CCTAGAAAAT ATGTAAGTGT AGAAGCATTT TAATGATGGC 60 TACTTAATGT TCTTTATCTG ATAATCCCAA GTCATGATTC ATCTCAGTGC TGCTGTCAGC 120 TGATGGTCTT TTCTCACTTT TGTGTTTTTT ATGGTTCTTC CTATCATTAA TGGCTTTCTG 180 TTGTGTCTTG GATATTTTGA ATATTATGCT TGGCAGCTTT TGATTCTATT TCAACTTCTG 240 TTTAAGTTTA GGTCTTGCCT ATTTTTGTGA GCTATTGGTT CAATGACCAT TTAATTTCAG 300 AGCCCTTGCA TATTGTTCTA GCTGACTTTG TTCTTCTGCT TCTGCTGGGC TCTCACTCAA 360 TCAATCCCTG AAGAGCTTTC AGTGTGAATG GAGGGGTAGT TTTGGAAGCA CTGGGTTTTA 420 GTTGCTGCTG CAGCTGATTG GCCTGCCACT GCCTTGGGTT TGGGGTAGAT CACTTCATTA 480 GGTCTCCGCT GGACCACCCC TTTCTCAGTT CTTCAGCAGA GGAGCAAGTA TTTTTATTTG 540 TCTATTCCTG TAGGTGGTTC AAGGCTGCCA AAAGGCTGCC TTTTTGATGT CCAGTCTGTG 600 ATATATGAAC CATAGCAAAA AAACGCAAGG AACTCACTCT GACATCATCC CTTAAGGCTT 660 GACATTTCTA GCCTTCTTCT CACTTTTTCA AATTCTTTTA TGATTGTCTG CTGAATTAGT 720 TCCAGGATAT TTAGCTATTT TTAGAGAGGA AGAGCAGAGA GAAGTAACTC TGTGTCATCT 780 TGTCCCTGAG CTGGATAGAA CTTATTATTT TTACAACAAA AAATTCATTC CCTCCAATAA 840 GAACAATCTT GTGTGTTTAA AAAAATCAGA AAATAAAGAT AAGCAACATG GAGAAAGTAA 900 AAGTAGATAC CAGTATTCTC AGATTGTTAA CACATTGATG GATTTCCTTT CTGATCTCCT 960 CTGTATGTGT AGTTTTGGAA AAAGTTATCA AGTTTTGTAT ACGTATACGC TAATGTATCT 1020 TAAACGTAGA CATTTTTAGT TTGCAAAGAA GACACATTGC TAAGTTACTT AAGTGAGGAA 1080 AGCTAAGATT AGAATATGAA GAAATCAAGA AAGCTGTCTT TATCGTTGTT CAGACATTCC 1140 AGGTACCAGA CTTTAAGAAA GACTGGAAGA ATGTCTCATT TTCAAGAGGC AAGGCAAGCT 1200 CAGGGGACCT CCACCACTAG TGATTGGGCC ATTTCATCCC CTTGACACAG AGATCCATTG 1260 GTCCCTGCTA CTCTCTTACT GTTCCTAACA GAGAGACTTT GTTTGGATCA GTTTTCACAT 1320 CACTTAATAC GGAGCATGTG TACTGGGCAG AGTCTTGAGC CAAGCCACAT GATAGGAAGC 1380 TAGTTTCCCG TATGACCACG TTACACAAGT TCACGCTGGT CTCTTATGGC TCAGGCCCAA 1440 GTCTCACACA TTGTGAACAC AGTAGCAACG TTCATATAAC ACTATATACT ACATTTTACA 1500 TGGAAAAAAA CTACCTGTGG TCAATGTCTC ATGAAAGAGT TGTGGGAGGG GAGATACACT 1560 GGGAAACCCA GGCCTGTATA TTTCAAATAT TTAGAACATT TGGTGCCAGG TGCAGTGGCC 1620 CATGCCTGTA ATCCCAGCAC TTTGGGAGGT TGAGGTGGGA GGATTACTTG AGCCTAAGAG 1680 TTCAAAATCA GCCTGGGCAA CATAGCAAGA CCCTGTCTCT ACTAAAAATA AAAAAAAATA 1740 GCTGGATGTT GTGGCGTGTG TCTACAGTCC CAGGTAATTG GGAGGCTGAG ATGGGAGGAC 1800 TGCTTGAGGC TGGGAGTTTG AGGCTGCAGT GAGCCATGAT TGCACTACTA CGCTTTAGCC 1860 CCTTTTTTTT CTCAAAACAA ACAAACAAAA AGCAGAACAT TTGGGTTGAT TTCAAGTTTT 1920 TACTAATGTG AAAAACAGCC CTGTGGCTCA TCTTTGCACT AGTCTTTCAC ATCCACATGG 1980 ACATGAGTGA CTTTCACAGG TAATAATAAT GACAATACAA ATCACAATTG CTCATAGGAC 2040 ATATAGAACC TCAACAGCTG TCAGTTGAGA AAATGCATTC ATTTTGCTAT ACTTTTGCAG 2100 AATTCTTATG CCTGAATATC ATATAACAAA TAACTGAATA TATCTCAGAG GCAACCGAGG 2160 TTCATAGAGC CAAGTGATAC ACCCAAAGGC ATGTGACTCA ATTGTGGAAA ATTCTAAGGG 2220 TAAACTTCAG GCCTGGCAAC ATCTAGTCTA GGTGTCTTGC TACTATGCTG TGCTGCCTTT 2280 CTCTTCTCAG AAAAAAGTGT TCTTAGGAGA CCAAGGCTAC AATGCTGTTT AGAAATCCCT 2340 CTTATTCACA TTTTAGGGAG ACTTTGAACA ATAAAGGTAA AACAAAAAAT AAGGTTTTTC 2400 TGGTTGACTC 2410
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