Tag | Content |
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EnhancerAtlas ID | HS133-03991 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:244093970-244095640 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RORA(var.2) | MA0072.1 | chr1:244095401-244095415 | TTAAAGTAGGTCAC | + | 6.05 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 244094400 | 244095000 | chr1 | 244095000 | 244095200 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I243930 | chr1 | 244093733 | 244095295 |
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Enhancer Sequence | AGCTGGGATT ACAGGCACCT GCCACTACGC CTGGCTGATT TTTATACTTT TAGTAGAGAC 60 GGGGTTTTGC CATGTTGGCC AGGCTGGTCT CGAACTCCTG ACCTCAAGTG AGGCACCCAC 120 CTAGGCCTCC CAATGTGTTG GGATTACAGG CGTGAGCCAC CATGCACCCT GCTGGAATCT 180 TTCTTTCTGC TTCTCTCTTG AAGGCCTTTC TTATTCTAAG TTTTACCCAG TGGCATCCTG 240 TGGAATATTA GAGACAATAG TCATCCCAGG AGTAGAAAAT TCAGTCCCAG CTGCCCTGTT 300 TTCCTCCTAA CCCTGCAATT TTGGACCGGA TCCTGCCATC CTGAGCAGCC AGTGAGTCTG 360 AAAGAGAGGG CTAATTCTAA TCCTTTCCCC TGGGACCTCT TAGTGTGGAT TCCTTTTTTG 420 TTGTTGTTGT TGTTGGTTTG TTTGAGCAGA GCCACTTTAA CTTTTAAGGG GCCCCCAAAG 480 TGTTTTCTTG AAAGGGCTGG GTTGGGAGGC CCCCTCTCGG GCCCCAGGCT ATGGCCGGGC 540 CACTTCCTCC CCTCATCAGA ATGCACCACC ACCCCCAGAC TGGAGAGTGT GGGAAGAGCT 600 GCCTGGGACG CTGTGGGTCG AGGAACTTGC TGGAATCTCT GCCACGGGGC CCAGAGCTAC 660 CCCGTGCATG ACAGAGAAGG ACTTAACGAG TGAAGGAGGC TGGTCTCCTG CGTGTCTTTG 720 GACCTGGAAA GGGAGAGGAA TTATAAATGA CTCAGGGAGC ACAAAGAGGG GATTATGGCC 780 CTGGCCGTGA AAGGGAGCGA GCCGGCTGAT AATGCACTGC TGCAGCCTCG GCTCATTCCG 840 CTCATGCCTT TGAAGATTTC CCTGCAGCCA GTGGCGCAGG AACACAACCC CGTGGACACG 900 GAAGGGCACC ACCGCGGCCC CTGGCAGGCC TCACCTGTAG CCGCTGCGCC CTCCCCGCGG 960 GCACCGGGCT CTGCATCCAG GAGGCTCCAG GAGGCCCAGG GGCCTGTGAT TCCCCGCAGC 1020 TCGGTCCATG TTAGCCGCCC CAGGCCCTCC TCGTGATTCC AAATAGAGGG GAGCGCGGTG 1080 CCCATTCCTT GTTTCTTTCT GATTGCTTAC CGCCCGGGCC AGTTGCACAG CATGCGGCCG 1140 AACTGCGGGG TGGTTAAGGA GGGACAGCTT ATGAAAAAGG TAGGGGTTGT GCAAAAGAGA 1200 AAACTCCAAG CATACGCTGG AGTTTTCTTA AAATGCAGAT TCAGATCTGA TGGCATAGGG 1260 ATTTCACTCT GCTGCAGAGC TTTCCATGAC TTATCTTAGA ACGGAACAAA CATTTGATGC 1320 TTGGCCTTTT ATGTGCATAA TCTATCAGTT TACAGGTAAG AGGACTGAGG TGGAGAAAAT 1380 AGCTACATGA CTAGGATTAG AACTCGGGTC TCTGGCTTCC TGTTATGCCT TTTAAAGTAG 1440 GTCACGCAGC ACTTTGGGAG ACCAAGGCAG GAGGATCGCT TGAGCCAGGA ATTTGAGACC 1500 AACCTGGGCA ACACAGCAAG ACCCCATCTC TACAAAAAAT GTAAAAAGTA GCTGGGCATG 1560 GTGATGCACC TGTAGTCCCA GCTACTCCAG AGGCTGAGGA GGAGGATCAC TTGAGCCCAG 1620 GAGTTCAAGG CTGCAATGAG CTAGGATTTC ACTCCAGCCT GTCTCTTAAA 1670
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