Tag | Content |
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EnhancerAtlas ID | HS197-00954 |
Organism | Homo sapiens |
Tissue/cell | ZR75-30 |
Coordinate | chr1:76137460-76139670 |
Target genes | |
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) |
BCL6B | MA0731.1 | chr1:76139603-76139620 | TGAATACCTGGAAAGCC | - | 6.1 | NFE2L1 | MA0089.2 | chr1:76138691-76138706 | GTATGACTCAGCACA | + | 6.94 | Nfe2l2 | MA0150.2 | chr1:76138689-76138704 | AGGTATGACTCAGCA | + | 6.85 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I075671 | chr1 | 76137630 | 76139428 |
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Enhancer Sequence | ACAATAGAAA AAGCTGATCT CGAACCAAGC TGTATTCTGA TACAGGCTGA AGTTTTCTGA 60 AATGGCTGTA GAGGAACTGA AACTATTTCT TTTTATTTTC ACATGGATTC TTAAAATAAT 120 TCTTATTAAT AATACCTAAT ATGCGTTAAT GGAAGACTAA CCATAACCTT ACATCATACA 180 GAAAGTTCCA ACTTGGAGGA CGTAGAGCAA CATGGCCTTC TAGAAACCTC CAGTGATCAT 240 TTCCACCACA GCAACACCAA ACTGACCAAC TATCCACCCA AAAAAGCACC TTCATAAGAA 300 CCAAAATCAG GTGAGCAATC ATAGTGCCTG CTTTTTGTTT CTTTGTTTGT TTGCCATGCA 360 AACCAACAAC TTGCAACAGT ATCTGCTTTT AACATGTCAG AAAAGAGGCG CTGAAAAAGG 420 CAAGTACCAA ATACAGGCTT GAATTGCCTA TGCCACCCTT CCCCCATCCC CTGGAGTTAG 480 CCACATGTCA CAGAGGGAAA AATCTGTGTA CTTTGGGGAG GGAAAGCACA GTGATTGTAA 540 GATTTGCATT GGAATTCAGT GCCGCACTGT CACAGTGGAA AGCAACAAGG GGCAAAACTC 600 AGCCTGGGCC CACAGAGAAA GCATTTAGAC CAGCCCTAGC CAGAGGTGAA TTATCCATCC 660 CAACAGCAAG AACCTGAGAT CCAGAGAGTC CCACCACCAT GGGCTAAAGT GCTCTGGGGT 720 GCTTAATAAA TTTGAAAGAC AGTCTAGGCC ACAAGGACAG CAATTCCTGG GCAAGTCCTG 780 GTCCTGTGCT GGTCTTGGAG TCAGTATACT TGAAGTGCAT GCAACCTAGT GAGACAGCAA 840 CCAGGGCAGC CAAAGGAGTG CTTGCATGAC CCCTCCCCAA AACCTAGGCA GCACCAATTG 900 CAGCTCTGGG AGAGATTCCT TTTCTCTGCT TGAGAAGAAG AGAAGGGACA GTAAAGAGAA 960 CTTTGTCTTG TAACTTGATA CCACCTCAGC CGCAGTAGAA TAGGGCAACA GGCAGAGTCC 1020 TGAGGCACCC ATTCTAGGCC CTAGCTCCAG GATGACATTC ATAGACATGC CCTGGGCCAG 1080 AAGGAAACTC ATTGCCTTGA AGGGAAGGAC TCAGTCCTGG CAAGATTAAT AACCAGCTGA 1140 CTTGAGAGCC CTTCAGCCCT GACTAGTCAG CAGTAGCCCA GTAGTACTCA CCATGGGCCT 1200 TGGGTGAGAC TCAGAGCTCT GCCGGCTTCA GGTATGACTC AGCACATTCC TAGCTATGGT 1260 GGTTTTGAGA AAAGACTCCT GCTTGAGGAA AGAGCAAGGA AGAGTAATGG GACTTTATCT 1320 TGTAGCTTGG TTACCAGCTC AGCCACAGTG GGGTAGAGCA CCAACTGGGC TCTTGGGGTC 1380 TCTGATTCCA GGACTTGGAT CCTGGATGGC TTTTCTAAAC CTGCCCTGTG CCAGAGGGGA 1440 GCCCACTGCC CTGAAGGGAG AGACTGAAGA GGTCTTGGGC CTTGAGTGAA TATTGGCAGT 1500 AGCTAGGCTG TACTTGCTGT GGGTCGGGGG TGTGATGACC ACAAGGAAAA CTCTGCTTGA 1560 GGAAGGGGGA GGAAAGACTG GGAAAGACTT TCTCTTGTGG CTTGGGTTCC AACTCACTGT 1620 AGTAGAATAG ACCACCAGGT AGATTTCAAA AGTTCCTGAC TTCAGACCCT AGCTCCCAGA 1680 CAGCATCACT GGACCTACTA GGGGAAGGGG GGAGCTCACT GCCCTGAAGG GAAAGACACA 1740 AGCCTGACTA GATTCTCCAC ATGCTAACTG AAGAGCCCTT AGGCCTTGAG TGAACATAGG 1800 TGGTAGGTAG GGAGTGGTCA CAGTGGGCTT TGGGCAAGAC CCAGTGCTGT GTTGGCTTCA 1860 GGCCTGACCC AGCATAACCC CAGTGCTGGC GACCACAAGA GTGCTTGTGC CATCCTTCCC 1920 CAAGCTCCTA GGAGCTCAGA ACAGAGAGAC TCTGCTTGTT TAGGGAAAGA TAAGAGAGGA 1980 GAACAAGAGT CTGCCTAGTA ATCCAGGGAA TTCTCCTGGA TCTTACCTAA GATCACCAGG 2040 GTAGTACCCC TATGAGTCTG CAAGAGCCAT TGTTTCACTG AGCTTGGGGT CTCATAATGC 2100 AGATATGACC CGAGAGATTT TCATCACAAC ACTTAAGTCC CTTTGAATAC CTGGAAAGCC 2160 TTCTGAAGGA GGACAGGTAC AAACAGACTG CAAAGACTAT AATAAATACC 2210
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