Tag | Content |
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EnhancerAtlas ID | HS133-06680 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr11:125070080-125072680 |
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) |
Hnf4a | MA0114.3 | chr11:125070312-125070328 | CTTTGACTTTGACCCT | - | 6.03 | RREB1 | MA0073.1 | chr11:125072600-125072620 | GGGGAGGCTGTGGGTTGGGG | - | 6.09 | ZNF263 | MA0528.1 | chr11:125072013-125072034 | AGGGGAAGGAGAGGGGGAAAG | + | 6.14 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr11 | 125072600 | 125072629 | chr11 | 125071293 | 125072600 |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I125201 | chr11 | 125070981 | 125072437 |
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Enhancer Sequence | GCCAAAGCAT TTTGTTCTCC ATGGTCACAG CCATTAGTCC CATGAAGAAA TAAGGCAAAG 60 GGATGAGCAG AGAGTCCCTC CCAAGGGTTA GAGGCAGGGG AGGGAGTAGA AAGGACCAGG 120 CCAGCTTGAT TTCCTCCCCC TACACCTTAA CTTGTGCCTC CCCAACCTGC CCAATCTCAC 180 CGAATAGCAG CAGAATTCAC CAAGTTTCTG CCGTCAAAAA CCTGGGCACT GGCTTTGACT 240 TTGACCCTTC CCTCGTTTCC TCGTAGCCCA GTGATAGGTT CTGTGAATTC CACCTGTCAT 300 GTAAGGTGTG ACTCTTGGCC CAACCATGGC TCTCCATGCA CCATGCCGCC CCCTGAGCCC 360 AAGTCTCTGC CACCGCTTGC CTGGCTCATT GCAGTGCCTC CCGCCGGTTC CCAACCTCCC 420 CCTGGCCCTC CGTCTGTTCT CTACACTGAA GCCACAGCCG TCACCCATGC CCATGTTTCT 480 CCTGCACCAA GGCCACCACA GTCTGCAGTC ACGTATGTAT TTATGTGATG TGGAGTTTAT 540 TGTCTGACTT GCCCATGAGA CGTGCTCCAG GAGGTCAAGG GCAGGGCCTG GGTTGACCGT 600 CACTGCATCC CCAGTGCCCT TGATGAGGAA CGGTTAAGCA ACTGAGTGAA TGACCCAGGC 660 AGGGCCCTTG TTTCCTTGCT GTCTCTTGCT TCTTTTCCAA AGGGACTCCC CCTCTAGACC 720 GTGTGATCCT CATGGGCAGG GGGTCTCTGC CTTTTGTACA CTGCACATCG AGGGACTTGG 780 TAAAGCTTTG GTGAATGAAT CGTGAGTCTC TGAAGTAGAG AACTTGATGG GGATCCCTTA 840 ATGCAGACCA CTGTCCTCAG ATTCAGCCTG GGGCCACCTT CTCTGTGCCA TCATTGCTCA 900 TTTTAGCTCC TTCTCACTGG TCTCCCAGGA CCTTGGTTTC CATGAACCCT TTCTGACCTG 960 AGAGCTTAGG CTGGGGCTGA ACCCAGATTG CTGCTTGGTT ATGGCCATTC TACCCCCAAG 1020 AGGAAGCGGG GTCTTCCTTT CCACTTTCCA GTGGGGTTTG GAAGCTAGAG GAGACATGCG 1080 GGAGCTCTGA GTGAAGCCCC CTCACTGCTG ATGCCTAGAG CCTTTGGCCT GATGAGCTCT 1140 TCAGAACCTC TGTGACCTCT GGAACTGCAT CCTTCCCAGA TATTGCTTTC TTCCTTGGTA 1200 GAAAAAAAAA AAGCAGCCTC CCTCCAAAGT TCTGGGGACT TCCAGATGAT ATGGAAAATG 1260 TCCACAAGGA ATGGCCACAG AAGAGCAGGT AAAGCCCTGG AGAGAGAGTC AAGGCTGGCT 1320 GGAGAAGGTG CCTGGTGCTG TGTGATTTGC TGCCTGTGTC CCTCTCCGAG CTGGAGTTTC 1380 CACCTGTGAA AGGAAGATTG CGCCACCTGT GCGGCTGCCA AGCTAAGGAG TATCTGACAG 1440 ATTCACTGGA AGCAGGAAGT GTGCCAGCTG GAAAATGGTG ATTTTTCATC CGACACCATC 1500 AGGAAAGCCC CAGACTTCAC CCCCTCCCTC TCTCCTGTTA TTAATGGCCA TGTGGATCAA 1560 ATTCCTCAGC CTTACTTCCT TCAAGGTTTT CTTCCAGAGC CTTATCTCAG GCACTCCTGG 1620 CTCCTTTTAG TTTCTTTCCT GCTGGGTAGG CATTTCCCCC AAGAGCCCAG TGAGTTTAGC 1680 ATCAGCCTAG GTTGGGGAAG AATGTGGGCT CGGCTGGGAG GCTGGGGGTC ACGAGCTGCC 1740 TTGTGGCTGC TCCTTGGGGT CTGGTGGAGC CCCAGCCTCT GGCTGTGACA TACAGCCCCC 1800 TTCATGAAGC CAGACAGAAT TAAGCCTTTT GTTTCCTGTT TGCTAGGCCG GCTTAAAGAA 1860 AACACAGAGG GTCCGTGCGG CTGGGACTCC CAACAAGACG GCCTTTGTAT TCATTTAATT 1920 AATCAGTTAG CTGAGGGGAA GGAGAGGGGG AAAGTTCATG TTATAAATAC ATGTTTTTCT 1980 TTGGCTTCCC CTCCTGCAAA AGACACAGCC TGAATGGCAT CCCCAAGACA GCCCCCCATC 2040 TCGCTGCAGA CATGCTGAGG GCCAGGGGCC AGCCAGGCTG CAGCTGGGAC CCTCCTTGCC 2100 CCTTTGCTTG CCCTGCCCCC TGCACCCCTC ACCAAGGGGC CTTATCCCTG ATGGCTGTGT 2160 GTCCTGGGGG AATGTTAATG CTGATGGGGT GGGCAAGGAG TGGTGACCAC TGGCTTCTAG 2220 AGCCCATCCT TCCTCTTTAC CTCTCCCCTC AGACCCCATA CCCTCCAGGG ATGAGGTGGC 2280 TGCACTGCCA TGTGGGTGAA GTGTCTGTCC CCAAAGAGGT CTGGGCAGTT GGCAGGTGCA 2340 CCGTGGAGAA GAAGTCCAGG CACACAGAAG GGCTGAAACT GGCACCAAGG TGTCCAGGCC 2400 GACAGAGTGC TGAGCACTGG CAGGGGACAC CGAGGGATGT CTGGCATCCT CCATCCCACC 2460 TTCCATTGGA GCCTTCTGGA GTGCAGGGGG AGGAGCCGTG GAATGTGCTC TTAGGGCTCT 2520 GGGGAGGCTG TGGGTTGGGG GGGAGGGGTG AGTGCTCTGG GACAGATAAT TTCATCACCC 2580 CTTCAGGCTC CACAGAGCAT 2600
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