Tag | Content |
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EnhancerAtlas ID | HS192-00283 |
Organism | Homo sapiens |
Tissue/cell | U2OS |
Coordinate | chr1:26489520-26491380 |
Target genes | Number: 21 | Name | Ensembl ID |
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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) |
CTCF | MA0139.1 | chr1:26490853-26490872 | TGCTGCCACCTGCTGGCGA | - | 7.78 | Stat4 | MA0518.1 | chr1:26490409-26490423 | CAACTTCCTGGAAA | - | 6 | Zfx | MA0146.2 | chr1:26490078-26490092 | CCCGCCTCGGCCTC | + | 6.01 | Zfx | MA0146.2 | chr1:26490835-26490849 | GCCGCCGCGGCCTG | + | 6.93 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I026163 | chr1 | 26490178 | 26491870 |
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Enhancer Sequence | TGAGGCAGGA GAATCGCTTG AATCCCAGAG GCGGAGGTTG CAGTGAGCCG AGATCGAGCC 60 ATTGCACTCC AGCCTGGGCA ACAGGGCCAG ACTCCGTCTC AAAAAATAAA AATAAAAATA 120 AAAAAAGAAA AGAAGGAAAC CTTTCCTGCC AGCCGGCAGG CTCCTGCCAC TGCCTCCCTT 180 TCCTGCAAGG ACACACAAGT TCGCCTATTT TCATCACAGG TTCGCACCTC CAAGCCTGCA 240 TCCTTCATGC ACCTCCTTCC TTTGCCTGGG TTGCCGTTCC TTTTCTCTCT GCTCTTCCTT 300 CTCTTTTTTT TTTTTTTTTT TTTTTTTTTT TTTGAGACGG AGTCTCGCTC TGTCGCCCAG 360 GCTGGAGTGC AGTGGCGGGA TCTCGGCTCA CTGCAAGCTC CGCCTCCCGG GTTCACGCCA 420 TTCTCCTGCC TCAGCCTCCC AAGTAGCTGG GACTACAGGC GCCCGCCACT ACGCCCGGCT 480 AATTTTTTGT ATTTTTAGTA GAGACGGGGT TTCACCGTTT TAGCCGGGAT GGTCTCGATC 540 TCCTGACCTC GTGATCCGCC CGCCTCGGCC TCCCAAAGTG CTGGGATTAC AGGCGTGAGC 600 CACCGCGCCC GGCCCCCTTC TTCCTTCTCG GAGATAACGT ATATTCTCCT CCAGGAAGCC 660 GTCCTGAATG CCCCCAGTCA GCCTCACCTG CTCTGAGCTC CCAAGTACAG TCCTATTTTT 720 GGGCCTCAAT TTGTCACCTT TTGTGGGACC CGCTGGTACT CTGGGTTCTC TAGTTAATCT 780 TTGACCTTTT TCCTAGTACA GGGACGGCGC ACATAGTAGG GCCACAGGCA CAGTTTGTTG 840 AATTAAATGA GGCTGGAGAG GGCGATGGAC GCAGTCCTCT GGAGCTCTCC AACTTCCTGG 900 AAAGTTGTAC CTTAAATAAA AAACCCATCC TGATATGCGG GCTGACTCTG GTCATTTTCG 960 CCTTGTATGT TTGATGAGGT GAGGACCCCT CCAGCTGGAC CCCGCCCGAG GTCGACCCCC 1020 GCAAAAGCAG TCTTTCTGGA TGTCTGGACA AAAGCACGCG GTCACACAGG CTGTCGGGCC 1080 AGGGTTTTTT ATCAGGGGTG GGAGCAGCGG GCGCGGGGTT CTGCCAGCCT GCTAGTCACC 1140 CTTGGGCGCA GCCTTCACCC TCATCTCGGC CAGTTTGTGA GTGAGGAAGC CCCACTTGAA 1200 GCCGGCCACC GGCTCGGCCT CCTGCGACTC GGGGCGCTCT GCGGCCTCCT CCGCGGCCTC 1260 GTCCGCGGGT TCGGGGTCCG GCTCCGGAGT GGGCTCGGTG CCGCGCAGCA TGGACGCCGC 1320 CGCGGCCTGC TGCTGCTGCC ACCTGCTGGC GAACGCGTCC CAGAAGCCCG GGCCGCGCGC 1380 CTCCGCCGCC GCCGCCGCCT GCGAGGGGGG TCGCGCCGCC AGAGGGCTGC GGGAGAGGGC 1440 CGCGGTCAGG GAAGCGGCCG GGCGGTCCCG CGGAGGAACA TCGGCTGGGC TGACGGAGGA 1500 GTTTAGTGGG GCCGGGGGAA CCTGGGCGGA GTCAGGGGCA GTGGTGAGGA GCGGGGTCAG 1560 GTGACCAGTG GGGGACCGGG ACGAGGAGGA GGGTCAGGGC CTGGAGGCAA GGGGAGGGCT 1620 CAGAGGCCCT GGGAAAGGGG TCTGGGGTGG GACAGGGTCA GGGGATTAGG CGAGGGATGT 1680 GGAGGGAGGG GACCGGGATC AGGATCCCTG GGGAGAGAAT GAGGTCAGGG TTTCAGGCGA 1740 GGCTCGAGGA GGGACGCTGG AGGCGTGCGC AGGTCTGGGA AGCTGGAAGG ATCCCTGGGA 1800 AAGCAGGTGG GAGCGGGAGG GCTGTTCAGA TCCCCCCTGA GGGAAGCCCT GGGGAAAAGA 1860
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