Tag | Content |
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EnhancerAtlas ID | HS133-01444 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:41233650-41235020 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFAT5 | MA0606.1 | chr1:41233933-41233943 | ATTTTCCATT | + | 6.02 | NFATC1 | MA0624.1 | chr1:41233933-41233943 | ATTTTCCATT | + | 6.02 | NFATC3 | MA0625.1 | chr1:41233933-41233943 | ATTTTCCATT | + | 6.02 | POU4F2 | MA0683.1 | chr1:41234312-41234328 | GTCATTATATATGCAG | - | 6.05 | ZNF263 | MA0528.1 | chr1:41234425-41234446 | CCTCCCCTTTTCTCCTCCCCT | - | 6.41 |
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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 | AAATAAAAAT TAAAAAAAGT CCGTTTTGGG AACAGAACTA AAGCCAAAAA ATGGGAGAGG 60 CTGGGGAGAA GCAAGAAAGT GGTAGCTGAA GGCAATGAAA ATCTTTGTAA CAACAGGTTG 120 TAATTATGAC AACCTAATAC TTAGTAGGTG CTCAGTAAAT GTTTGTTGAA TGAAGCTGAA 180 TGAATAATAT GTAAATAAAA TGTAAAGGTA AATGAAATCT CAGCTAATAT GAATGGCAAT 240 CCTGCTGGCC ACAGAGCAGT TAACCTTCTT ATCTATGTGG AATATTTTCC ATTTGTCTCA 300 GGCTCACTTG TTTATTCTGC AACATTTCTG GAATACTAAC TTTGTATGGG CTCCTGCCCT 360 CAGGCATCTT ATAGGCTGTT GGAAGGAAAA GGACCAAAAT AAGGAACAAT AGTAAAAAAT 420 AGTCATGAAG CCTGTCATAC CTGTTCCCTT TCTTGTTCCT CATAGCCTCA TGGGTAGGCC 480 TGCAGGGGTT GTTTTTGGCC ATGGTGAGGA CATTTGAGAG GACAGTCCTT GTCTTGCAGG 540 CTGGCTGTGA TGATTCCAGG AAATGGTACA CAGAGGACAC TGCTGGCCAA ATGTTCCATA 600 GGAACACATG TGCATGCACA CCGCAGTCTT CTTTCTAGTT TACCGAGCTG CTCCCAGCAG 660 TTGTCATTAT ATATGCAGTT CTACATGTCA GTACATTTAT CTAAAATCCA TTCACAGTCC 720 ACACATAAGA TTTTAAGTAC TTGTGATAAA TGTTGTCTTT GTTCCACTCC CGGTCCCTCC 780 CCTTTTCTCC TCCCCTCCTT TGGCCCAGAG GGCTGCACAG TGCCTCTCTC GGAAAAAGTA 840 CTTCATAGGT TTGCCATGAG GACTGCTGGG ACCAAGGCCA CTTGCTCGCC AGGGTGTTTC 900 ATATTCCAGT CAGATGATCT GGGTGATACG GGTTTGGTTT GGAGCCCACC TTCCAAGAAT 960 GAAAGAGGCC ACTTACCACT TTGTCTGACA CTTTGCAGTC CGCCTTCACT GGCTGAAAGA 1020 CTGACTCTTA GGACTTCTAC CCCAAACCAT AGCACCTAGG GTCCATGTGT TCTGTTTGAG 1080 CCTCAGAGTT TGAGATGAGT GGGTGGTTGA GGGAGTAGGC ATTCATTAGA GAGATGGGTG 1140 TGGGAACTAT CTATTATGTG CTCCAGGATT CTCGATGTCA CTTTGTGCTG CCAACTCTTG 1200 ACGTAGCCAT CAGTGCTAGA TTAGGAGGGG TGCTTGCTTG CTTACTACCC ATTGAGCACC 1260 TGCTGGGCAC TTTATATGCA TTGTCTCATT TGATCTTTAT GACCCTCTTT TGGGTGGTGG 1320 GCTGGTGGAT CAGACCCTGC AGCTGACATA CCAACTCTAC CATCTTGATT 1370
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