Tag | Content |
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EnhancerAtlas ID | HS133-13594 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr17:77997010-77999560 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr17:77997180-77997198 | CCTCCATGCCCTCCTTCC | - | 6.1 | Myod1 | MA0499.1 | chr17:77997129-77997142 | AGCGACAGCTGCT | - | 6.74 | RREB1 | MA0073.1 | chr17:77998380-77998400 | ACACCACACACCACACACCA | + | 6.14 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_27830 | chr17:77996905-77999920 | Fetal_Intestine | SE_28735 | chr17:77996920-77999951 | Fetal_Intestine_Large | SE_30858 | chr17:77996579-78000080 | Fetal_Muscle | SE_41917 | chr17:77997897-77999938 | LNCaP |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I080022 | chr17 | 77996654 | 78000875 |
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Enhancer Sequence | CACCTGCAAT AAAATACGTT TTCAGAAATT CACCAGATGT CCCTTCCAAA GATCAAGCCC 60 AGCTGCTCCC CTCCCCTTTA TGGGCAGGCG GCCCTCCAGG GGTATTGCGA ACGGGCTCCA 120 GCGACAGCTG CTCGGAGGCT ACCATGGGAC AGTACCCGGG CAGCCACAGC CCTCCATGCC 180 CTCCTTCCGC CCCGCAGTCC CAGCATGAAG CCACAGTTCC CCATGAGCCC AGGGCAAGCT 240 CGTCAGAGAC CCTTCCCTGC GGAGGCCCAC AGCCCCTGCG GCCACTTCTT CCCCGAATCT 300 CAATCCTGCT TCGTGTGGCC ACTGCTGAAA GAGACGCTCA GTGCCACTTA GAGCGCACAG 360 CCCACTGGTC CAGGCTGTGC ACACCCAGGG ACCCTTCCAG GCATTCCTCA CCTCGGTGCA 420 GGCCAGGAGC GAGAACTGCT GCCGGGCCCC CCCCCACCGG CTCAGGGCGT GGCTGGGGTG 480 GCCCTGCTCC TCGGTGGCCC GCCTGGCCCC GCTGTGGGCT TCCCTCCCAC CACCCCGGCC 540 ACAGTCACAG CGGGTTGTGT CAGGCCGCCC TCATCTCCCA CCTCCCAGGC CCAGCTGGCG 600 CCTCCAGCCC TGGTGTGAAT TTCCATTCAG GGTCCAAAAT CCACCTTGGC AGCGCCCTCA 660 TTCTGCAGCT CCACGGAGCC CTCCAGCCAG AGAAGAGAAA TCTGAGTTTA ACCCGATCCT 720 GTCAGAAGAG CGGGAGGAAA GAGCTCCGGC GGACAGGGCT CCCAGGCCCC TCCAGGACGA 780 GGTTGGAGGA CCAAGCGCAG AAGGTAAGGA CGCAGCCCTC GGCGAGTGCG GGCGGGGCCC 840 AAATCCCTCG CCGGCCGGCT AAGCAGAAGC GGCTTTTGGC TTTCCGCGAC AAAGCGCAGC 900 TCCGGGCCAG ACGGTCCTGC CCGGCCCTAC CCGCAGCCCC GGCCCCAACC AGAGGCCCCA 960 CTTCAGCCCA CCAGGCAGGA CTGCAGCGGG GCACGCCCCA CGGACCCCAG CCCCTTGGAG 1020 ATCCCAAACC CCATGCCTGC TGCTCCCACC CCGGAGGAGT CAGAGGCCGA GAAGCACACA 1080 CACCATAGAC CCCACACCAC GCACACCATA GACACACATA CCACACACCA CACACCATAC 1140 CACACACAAC ACACACCACA GACACACACA CCATACACCA TAGACACACA TACCACACAC 1200 ACCATAGACA CACACACTAC ACATCATAGA CACACACACC ACACACACCA TAGACACACA 1260 CACCACACAC CATAGACACA CACCACACGC ACCATAGACA AACCACGCAC ACCATGCACA 1320 CACCACACAC CATATACACA CACACCACAC ACGACACACC ATAGGCACAC ACACCACACA 1380 CCACACACCA TAGACACACA CACCACACAC CATAAGCACA CACACCACAC ACACCATAGA 1440 CATACACACC ATAGACACAC AGACACACAT GCCATAGACA CACATGCCAC ACACGACACA 1500 CCATAGTCAC ACCACACATA CACCAGACAC CAAGACACAC ACACTACATA CACACCATAG 1560 ACACACATAC CTACCACACA CTACAAACCA TAGGCACATA CACCATAGAC ACACGCACTA 1620 CATACACACC GTAGACACAC ACCACAGATA CATACATCAC ACACCACATA CCATAGGCAC 1680 ACTGCATAAA CATCACACAC ACACCACACA CCATAGACAC ACACACCACA CACACCATAG 1740 ACACACCACA CACACAACCC CGTAGGCACA CACCACACTC TACACACACA CCATAGACAC 1800 ACACACACAC CACAGATGCA CACATACCAT GACACAACCA GGCACACACA CTATGACACA 1860 CACACACATA CCATGACACA CACACACCAT ATACACACAA ACACCACAGA CACACACACA 1920 CCATAGGCAC ACACAAACAC ACCAGGACAC ACACACCATA GACACACACA TACCATGACA 1980 CACACGCACC CCATGACACA CACCACACAC AGCCACCCTC TGCTCTACCA GCTTTGCCTC 2040 TGTTCTCCGA CAGCGCCAGT GTTGACACGC CAGAGGCTGC CTGGGCCCCA CTCCTTCCCA 2100 GCTGTCTCCA GGATTAGGGA AGCCCCAGGC GGATCCGGGG CCGCAGGAGC CTCCCTACCC 2160 AGCCCCCATG CTGGTCTGTC TTGGGTCCAT AAACACAAGT CAGCCACCTG TCACCGGGCG 2220 GCAGGAAGTG CAGGCTCTGT GAGCTGGAGG AGGGGGCGCC TAGGCTCTGA GGGCTGAATA 2280 AGGGGCCTGG CAAATGCCCC CGGAGAGCCC TGGAGAGTTT TGCAGCAGTC CTGGCACCTG 2340 GGCTTCGGGG CCCGCCTGCT GGGAGCAGCC GCCTGCTGGG AGCACCTCCT TGCTGGAAGC 2400 ACCCCCCTGC CAGGAGCCCC CCACCCCCAC CCAGGAGCAC CCTCCTGCTA GAGTGCCAGG 2460 GAGACACTGC TGCCTAATGG CCAGGAGCTT GCCCAGGGCA GTGACTTCTG GTCCACTTCT 2520 GTCCCTTGGT TGTGTCCCTA AGACCCAGGG 2550
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