Tag | Content |
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EnhancerAtlas ID | HS133-28635 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr7:65511660-65513540 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF143 | MA0088.2 | chr7:65512648-65512664 | TAACCACAATGCATTG | + | 6.96 |
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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 |
GH07I066046 | chr7 | 65511902 | 65513450 |
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Enhancer Sequence | CGAAAATGTC CTAAAAGTAT TATGGATGGC GGTGGTGGTT GCACAACCCT GTGAATATAC 60 TGAAAACATT GAGTTGTACA CTTTAAATGG CAAATTGTAC AGCATATGAA TCCTATATTA 120 ATAAAGCTGT TAAACATTTT TTACTCGGCT GAGCATGGCG GCCCACACCT GTAATCCCAG 180 CACTCTGGAA GATGAAGGCA GGTGGATCGC TTGAGCCCAG TTTGAGACCA GCCTGAGCAA 240 CGTGGCAAAA CCTCATCTTT ACGAAAAAAA AGAAATTAAC CAGCGCAGTG GCTCGCACCT 300 GTAACCCCAG CTACTCAGGA GGCTGAGGCA GGAGAATCGC CTGAACCCAG GAGGCAGAGG 360 TTGCAGATCG CGCCACTGCA CTCCAGCCTG GGTGACAGAG CAAGACTCCA TCGCAAAACA 420 ATAACAACGG CCAGGCGCGG TGGCTCACAC CTGTAATCCC AGCACTTTGG GAGGCCGAGG 480 AGGGCAGACC ACAAGGTCAA GAGATCGAGA CCATCCTGGC CAACATGGTG AAACCCTGTC 540 TCTATTAAAA GTATAAAAAT TAGCTGGGCG TGGTGGCGGT CGCCTGTAGT CTCAGCTACT 600 TGGGAGGCTG AGGCAGGAGA ATCGCTTGAA CCCAGGAGGC AGAGGTTGCA GTGAGCCGAG 660 ATCACGCCAT TGCACTCCAG CCTGGGCGAC AGAGCGAGAT GCCGTCTCAA AAAAAATAAA 720 AATAAAAAAT TAAAAAACAA CAACAACAAC AACAAAGTGC ATAAAATGCC ACCCAGATCT 780 AGCTGGCCTG GTTAGTGTGG AGAATTCCCT GTACCTTCGT TGAGAAAATG GGGCCCCACA 840 AAGAAATGCT AAAGCTCCTC CTTGTGTTAT TCATTCAACA AGTATGTAGC CATGGCCCAT 900 CGGGGGCTGA TGATACAAAT GTGACTAACA CACACCCTCT GCACTGGCTA GCTGACAGCG 960 TAGTTGGGGA GCCAGCTCTG GACATAAATA ACCACAATGC ATTGTGTTTT GACGCGATGG 1020 GGCAGGGGAG GGAATGACTA ATGAGGCGGA GAGGCGTCCC AAAACCATGG GCCTTTGAAG 1080 TGGGTGAGGG GAAAAGCACA TGAGGCCGAG GGATTAGGTA TGGGCTTCAG TGGAAAAGAG 1140 CAGTGCCTCT GACAGCCCCC ATGATAAAAT GGCTCAGGTG TGACTTAGAG TAGGGAGTTA 1200 GCTGGGTGTT CAAATGGTAC CCAGGAGGCC GGGCGCAGTG GCTCACACCT GTCATCCCAT 1260 CATTTCAGGA GGCCAAGGTG GGTGGATCAC TTGAGTCCAG GAGTTCAAGA CCAGCCTGGC 1320 CAACATGGTG AAACCCCATC TCTACTAAAA ATACAAAAAT TAGCCGGGCA TGGTGGCTGG 1380 CACCCGTAAT CCCAGCTACT CAGGAGGCTG AAGTAGGAGA ACCGCTTGAG CCTGGGAAGC 1440 AAAGGCTGCA GTGAGCCAAG TAAAAGTTCT TTTTACTGTC TGCACCTCTG GCCCTGAATA 1500 GTCGCTGATC ACCATGACAA TTAAGGGTAT GGGCCTTGAG ATGCAAAGAA AAGATTATCC 1560 TGGATTTTCT ACATGGTATC AACCTAATCA CAGGGGTCAT TAAAAGCATA GAATCATTCT 1620 CAGCTAATGT CAGAACCCAA GGGAGGTGTG GCTAGGGAAG AATGGTCTGA GAGATGCAAT 1680 GTTCCTGCCT TTGATGGTAG AGGAAGAGAC CATGAGCCAA GAAGTGTAGG TAACCTCTAG 1740 AAGCTGAAAA AGGCAAGAAA ACAGATTCTC CTCTGAAGCT TCCAGAAAGG ACTGCAGCCC 1800 TACCAACACC TTGATTTTAG CCCAGTGAGA CTCATGTAGG ACTTCTGTAT TAGTCCGTTC 1860 TCACACTTCA ATAAAGAAAT 1880
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