Tag | Content |
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EnhancerAtlas ID | HS062-09533 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr2:174074820-174076350 |
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) |
Foxa2 | MA0047.2 | chr2:174075144-174075156 | TGTTTACTTTGT | + | 6.18 | MEF2A | MA0052.3 | chr2:174075396-174075408 | ACTATAAATAGC | + | 6.11 | MEF2B | MA0660.1 | chr2:174075396-174075408 | ACTATAAATAGC | + | 6.74 | NFIC | MA0161.2 | chr2:174075875-174075886 | TACTTGGCACA | + | 6.32 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_45738 | chr2:174073986-174076388 | Osteoblasts | SE_47134 | chr2:174073113-174076005 | Panc1 | SE_55735 | chr2:174074926-174076257 | u87 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I173209 | chr2 | 174074473 | 174076433 |
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Enhancer Sequence | TGTAATCCCA GCTCTTTGGG AGGCCAAGGC AGGCAGATCA CCTGAGGTCA GGAGTTTGAG 60 ACCACCTTGA CCAACATGGA GAAACCCTGT CTCTACTAAA AATACAAAAA ATTAGCCAGG 120 TGTGGTGGCA CATGCCTGTA ATCCCAGCTA CTCAGGAGGC TGAGGCAGGA GAATCACTTG 180 AACCTGGAGG CAGAGGTTGC AGTGAGCCGA GATCATGCCA TTGCACTCCA GCCTGAGCAA 240 CAAGAGTGAA AAACTCCATC TCAAAAAAAA AAAAATTGAA ATCCTGTCTT CTGAGACAAA 300 AGATGGTTAC CAGACATTTC TCTGTGTTTA CTTTGTTAGG AAGCTTTGTC CTCTGTTGTG 360 TAAGAAACAA GAATACTGTT TACCTTGAAA TTCGCTGAGC ACTGTGTCTG CTAGTGAAGG 420 GGGATAGGGA GACATCAAAA ATACTCTTAA AAGAAAACTT GATATCATAA ATCCTATTAA 480 AGCTTGTTAA ATAAATTTAG TAATGAGAAA ATTGTATTGC ATGAGTGGAA GAGTAAACCC 540 AGGATGAAAC ATTTGAGCCA GGTCACATGA TGCATGACTA TAAATAGCAT GTTTGGAAGC 600 TGACATTATT CCCCCCCTGA CTCAGCGGAG ATTTAGGTAA CTTCATCTCT GCTCCCGATA 660 GCCGTGGGCA GTAACATGAC GCCTTACGCC ATCTGCTGAT GCCAAATGAA TACTGCATGC 720 ACTTTGAAAA TTACTGCGTT GTTTACTCCT GTTACTAGAT ACTTCTTTGG GCTTTCTGTT 780 TGTTGTTTTA CAATAACCTT ATTTATTTTT ATTCCTTTGA AATATCTTAT CTAGGGCTAG 840 TGAGGTAAAT GAATTTTTAT TTAGGGATAC AAAAATTATA CAGTGAGCTC AAGTCTAGGT 900 ATAAGGGACT TTTTTCTGGG CTGAGATAAT TAACAAAACA GAACATTTAA GTAATATTTG 960 TTTTTTGCAG TAAGAGATCA GTATACATGT CATCAGATCA TTCTCCTTTA AAATCCATAT 1020 ATGAGTTCCC ATTACTCTTA AGACAAAGAC CAGAATACTT GGCACAGTGG CTCATGCCTG 1080 TAATCCCAGC ACTTCAGGAG GCCAAGGCTG GTGGATTACT TGAGCCCAGG AGTTCAAGCC 1140 CAGCCTGGTG ACAGAGCAAG AATCATTCTC AAGAAATGAA AAGGACCAGA ATACTTAAGA 1200 AGACTCACCA GACCCTCATT ACTGTGGCCT CACCAGTGTC AGCTTAAGAA GATCATTCTC 1260 CCCTTAATTT CTGGCTTTCA GTCCCTCAAC AGATGCGTAT TTCTCCCCTT TTCAGGATCT 1320 TTACAAGCAG TTTCCTCTCT TTGAAGCTTA TCCCATTTCA GCTGTGTACC ACGCCTGCCG 1380 TCACACCCCA CCTTAACTCC TGTTCATCAT TCACATGGCA GTTGAATAAC ACGTCTGCAG 1440 GGAAACACTT CCTGACCCCA GGCCAGATCA GGTTCCACTT TATGTGCTCT GAGAGCATCT 1500 CCTTCATAGG CTTTGCTGCT ATTGGAATTA 1530
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