Tag | Content |
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EnhancerAtlas ID | HS007-06946 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr17:30601990-30604160 |
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) |
E2F6 | MA0471.1 | chr17:30602479-30602490 | GGGCGGGAAGG | + | 6.62 | Nfe2l2 | MA0150.2 | chr17:30602284-30602299 | CCGGATGAGTCAGCA | + | 6.13 | TFAP2A | MA0003.3 | chr17:30603049-30603060 | TGCCTCAGGCA | + | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_69056 | chr17:30601644-30603172 | H9 |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I032274 | chr17 | 30601790 | 30603510 |
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Enhancer Sequence | CTTTATCCTT CCAGCCCTTT ATCCTGCCTG CCATGCACCC GCTCTGCATC TTGCTCCCCT 60 CCTTCTCCCT GGATCTGTTG GCTCTCTCTC CTCTGGGGGA CCAGAGAGAC CCTTTGGTGG 120 CTGCCAGGAG AAGCAGCGGC GGCCAGCAGT TTAGGCTGAA GGGGAGAGAT GGGGCGATGT 180 CAGATCCCTC CCTGCTGACA TTCACTCCCC ACTCCCTGCC TGCAGTTCCC TTGAGACTCC 240 TGGGCTTCAT GGCCATGACT CGGCTTCAGT CCCCAGGCGG CGCGTCAGGC TGGGCCGGAT 300 GAGTCAGCAT GGATGTTACA TCTGCTCCTC CTGGGTACCC AAGGGCCTCT GAGTCACAGC 360 CCCTGGCAGC CCCCTCAGTG GCCTGCCAAA GGCAGGGGCC ATTCTGGAAT GGGAAGGGAG 420 CCGTCTGTGT GCCTGGGAGG CCTTGTGAGG AGGTCGGAAG GAGGAGAAGG GGCTGCAGGA 480 GTCCCCCAGG GGCGGGAAGG AATAGGCCCA GTGGAGGAGG CAGTCCCCCA ACCCGTGCTG 540 CCCACCCCAC CCATCCCCAG CTGCATGCGT TCCAGGGAAG GTGTGAGGTC GTTTCTTTCC 600 CTCACTTCCC AGATGTTGGG AGAGCTGGAT GGTTTTCTGG AAGCATGCCG ATTGTCAAGG 660 GCTCAGCCTG AGTTCAGGCC AGGATGCCTG TCTCTCCCTA ATCAGCCTGG CTGCCCCATC 720 CTAGGATTCG GCTGTTCGAC TTTGGGCAAG GGGGATGCTC AGGAGGCTGC TTGGGGCTTT 780 TGGGAGAAGC ACCATGAGAG GGCTGAGCTG CCTCCCGCAC CCCTCTATGG TGGCAGCTGA 840 GGGAGCAGAA ATAATAAAAC TGGGAATCCC AGAATCGTGG AGGCTTCTCC AGCTGTCAGG 900 GGCCTGGCCT GGCCAGATCC CAGGGGAGTA GGGGTCACAA GGGCCCCTCA TGCCTCCATC 960 TGGTCTCTCT CCTTCCCACA GAGGCTTGAG GTCTCTGAAA ACCCACTCCC AGCCCCAGCT 1020 TGAAGCAGGC CAGACTGCCT GGGTCCACCC CTTCCAGAGT GCCTCAGGCA GGGGGCATGT 1080 CTCTGAGTAC CTCAATTTTT GTATCTGTTA AGTGGGACGA ACCAGACTTA CTCTAGGGTT 1140 GGCATGAGAA TAAAAAAACA AAACAAATGT GAAAGTCAGT ATTTTAAAGA GTCAGGGGAA 1200 AAGGTCAGGG GAAGGGTATG AGGTGGTTTT CTCTATGGGA CAAACCAGAC TTACTCTAGG 1260 GTTGGCATGA GAACAAAAAA ACAAAAAAAA TTGTGAAAGT CAGTATTTTA AAGAGTCAGG 1320 GGAAAAGATC AAGGGAAGGG TGTGAGGTGG TTTTCTCTAT GGGTGAATTA GCATCCTCAT 1380 TTGCAAGAAA GCAGAACTGG GAGAGAAAGC TCCTACTCCC CTAACCTCCC CGCTGACCTT 1440 GGCAGCTGCA GCCTGGACCT AATTTACGGG GCTGTAAATA TCCATGAAAG GGCCAGAGTT 1500 CCCTTTTGGG CTCTGGCTGT TGGGTGGGGA GAGCTCTGCT GAACCACAAA CCCCTGGGCA 1560 GCCTCGTTAA TTCTGCTCTG CTCAGAAGAC GAGTAATGAG GCAGGGGGCC AGCAGTTGAG 1620 CCATGGTAAC CTTCACCAGA CAGCTGCCTG CACCATACTT CAGCCCTAGC ACCGTACTCC 1680 AGCCCTAGCA CCGGACTCCA GCGCTAGCAC CGTACTCCAG CCCTAGCACA GTACTCCGGC 1740 CCTAGCACCT TACTCCGGCC CTAGCACCTT ACTCCAGCCC TAGCACAGTA CTCCGGCCCT 1800 AGCACCTTAC TCCGGCCCTA GCACCTTACT CCGGCCCTAG CACAGTACTC CGGCCCTAGC 1860 ACCTTACTCC GGCCCTAGCA CCTTACTCCG GCCCTAGCAC AGTACTGCGG CCCTAGCACC 1920 TTACTCCGGC CCTAGCACCT TACTCCAGCC CTAGCACCTT ACTCCGGCCC TAGCACCTTA 1980 CTCCAGCCCT AGCACAGTAC TGCAGCCCTA GCACTGGACT CCAGCCCTAG CACACGTGCC 2040 TGTGCTCATT TCCCAGGGCT CATTCTGCCT TGGTGTGTGT ACATGGGAGA AGACAATGGG 2100 GATCCGGGTG GGAACCTGCT CTAGATCCCA GGTCTCCACC TTCCTGACTC AAGAGGTCTT 2160 TACCCCAGTG 2170
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