Tag | Content |
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EnhancerAtlas ID | HS133-29615 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr7:127742400-127744890 |
Target genes | Number: 12 | Name | Ensembl ID |
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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) |
NR2F1 | MA0017.2 | chr7:127743944-127743957 | CAAAGGTCAGGGG | + | 6.13 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_58728 | chr7:127743411-127776818 | Ly1 | SE_60951 | chr7:127740843-127758458 | DHL6 |
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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 |
GH07I128103 | chr7 | 127743353 | 127745052 |
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Enhancer Sequence | CTGGGGATCT TGTTAGAATG CACATTCTCC TTCAGTAAGT ATGGGGCAGG GCCAAGAATC 60 TGCATTTCTA ACCGGCTCCC AGGAGGTGCT TTGGGCCAAA GGACCACCCT GAGGAGCTAT 120 CCCCTCCCCA GCCCTTTCAG GCCAGAGGCT ACCAGCAGGA GGTAGTAGGT AGAGAAGCCC 180 ACCTGGTTCC CACAGAGGGC TCCTGGGAGG TCTGACCAAG GCCTGAGTTT GGAGGCAGGG 240 AGCAAACAAG ACTCATGCTA CCTAAAGCCA GAAATATAAG GGAAAGAGCC AGACCCTGGC 300 ACAGCTCTGC AGGAGAAGCT GCCTGAGGAG AGGGGCTGGG GCTGAGGCTG GTGAAGAATC 360 TCTGCTCTAG GAGCTCCAGG GCCAACATAG AGTGCAGGCA GAGCTAAGCT CTGGAGTGTA 420 GGCTCTCTAG ACTGTACACC TCCAAAATGA TCATGATGTC AGCAGCAGCT CAAGATCTGT 480 GTGCTCCCAC AAGGGCTAAG CACTTTATGG GTAGTCTTAT CAGGGAAGGA CCCTTCCCCC 540 GGTTTTACAG ATATCCTCTG GAAGACAGGC CTAGAGTCCA TGACTTGCAA GTATTCAATA 600 AATGATTTAT GAGTGAATGA CTAAAAGTGC AGCTGAGTCC TGGCAGAGGG CATGGGGTCC 660 CACCCAGAGA CAGGCAGAGA AAGTTGAAGT CCCAGGATTG GAGGCCGTTC TTCCTCACCT 720 CCCCACCAGG CCCAGGCAGG GCTTGATCTG AACGGAGGCC TGGGAACCTG TGGCCAGCCT 780 TTACTTGTTG GAAAAGAGCA GTCCTTAAGC TCAATTGCTC CAGGTTGATG CTTCCCTACT 840 TTTTTTTATT TATTTATTTT TATTATTATT TTTTTTTTAT TGAGACGGAG TCTTACTCTG 900 TTGCCAGGTT GGAGTGCAGT GGCGCGATCT CGGCTCACTG CCACCTCCGC CTGCTGAGTT 960 CAAGCCTCAG CCTCCTGAGT AGCCTCCTGG GTAGCTGGGA CTACAGGCGT GCGCCACCAC 1020 GCCAGGCTAA TTTTTTGTAT TTTAGTATAG ACGGAGTTTC ACCACTTTGG CCAGGATGGT 1080 CTCGATCTCC TGACCTCGTG ATACTCCCGC CTCGGTATCC CAAAGTGCCG GGATTACAGG 1140 CATGAGCCAC AGCGCCCGGC CCCTAGTTCT TTTTAAAAAA CGCTAGATCC GTCCGCTGCG 1200 CTGAGTGGAG GCGGGGCAGG CCTCCGTTCT CCAATTGGCC TTATCCACCG AGCTCTCCCC 1260 TTGTGCCGGG CTCTGTGCCA AGCACATCAC ACGCTGTATC CTGCGGCCAG GTTGCTGTGG 1320 TCCAGGGTCG TACCCTGGTC CAAGGTCGCA AACCGAGGTG GGACTCCGAT CCGGCAACCA 1380 CGCCCGTGGC CCGGAAACGG CGTCCCCTGA GGCCCAGGAG AGGCCGGGCG GTGAGCGGCT 1440 GTGGAGCCGA GCGCGGGCAG TGCGGATGCT GCCTATGGGG GAGGCAGCCA AGGACGGAGG 1500 GCGAGAGGCG GTTCTTCCAA GGTCACCCTC TTCCGGGTTG CAAGCAAAGG TCAGGGGATC 1560 CCGGAATGGT TAGTGCAGGA GCTTCTCTGT GCCTTCCACG TCCTAGATCC TCAGAGCCTC 1620 AGAAACGGAG ATCATCGTCC CCACCCCCAT TTTACAGATG AAGAAACTGA GCCGAGGAAA 1680 GGAAGCGACT TGGCCAAGGT CGGAGAGCTC ATTCTTTGCA GGGCGGGGTT TGGAACCCGG 1740 GGTCTGGCTC TCGGCAACGC GCCCTCGGCC CGCAGCCTCC TGCCCCCTGT GCCCCGCTTC 1800 GGCCCCCAGC GCAGCTGCAG AGGGGCCCCC CTCGACGCAT ACACTCAAGA GCCCGACCGC 1860 GCGGCTGAAA TCGCGGAGCT CGGAGCCGCG GCTGGCTGAG CGATCGCGGT TCCTGGGCTG 1920 CGTGCGCGCC CCTTGGAGCT GAAAGGAGCG CCAGGATCGG GGGCGCTGCA CCGGGCTGGG 1980 CCCCTCAACG CTCGCAGACC GGGCCGGGCT GCAGCTGGAG ATGGCAGCAA TCCCGGGAGG 2040 TCTCCGGGCC TCTTCAGGGT GCGTCCAGGA GGCGGGTTCC GTGCGACGCG GCGCAGCCCA 2100 CCCCCACGAG ACCGCTTAAC TTCGCGGGGG CAGCCTCGGG CGCTCGGAGA CGCGGAGGCC 2160 CAGACTGCAG CCTCCGGATG CTGGAAGCCC AGACTCCCTG GGGTCACCGG CTCTCCCGCC 2220 ACCCCAGCTG CAAAGAGTCC CATTGCTTCA CCGTCCGGAG CTTAGTCTCC TTGTTCCTCT 2280 ACCAGTCCCT CCCTCCGCAG GTCTCTGGGG ACTTCTGACC GCCTGTTCTT ACTCTCCCCC 2340 TGCCCCCATA CTTCCCGCCC TTGTCTCAGG AACGGTGATA CAGTCATCGG ATTGCTCTCC 2400 ATCTCCTGTT AGTCTACACT GCACACAACT CAATAATCCG CTCCCTTCAT CCGGGTGACA 2460 GAGACACAGA TAATCTGAGC TAGTGGTGCT 2490
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