Tag | Content |
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EnhancerAtlas ID | HS007-02499 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr10:122838870-122840600 |
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) |
CDX2 | MA0465.1 | chr10:122839890-122839901 | AAGCAATAAAA | + | 6.32 | Foxo1 | MA0480.1 | chr10:122838951-122838962 | TGCTGTTTACA | + | 6.14 |
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| Number: 1 | ID | Chromosome | Start | End |
GH10I121076 | chr10 | 122836333 | 122840976 |
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Enhancer Sequence | TTGTGTGAAG GAAGGCTCCA GTGATCAGGT TGCTGCAAGA TCAGGTTGAC TTGGGGTAAT 60 AACCGCAGTT GCAATTACAT GTGCTGTTTA CATACTTTGC CCCTTGTACT TGATAAAGTC 120 CAGAAAGAGC CCTGGGCGCA GCTGCTCAGC GCCTCTTGGG GGTAAGCCAC ATACCCTGTG 180 GGAGCAGGAG AGCCACCTCT CCCCTGAGAG AGAAATAGGG CCCAGATAAT GTCTAGTTTA 240 GGTACCTCTT CAGACCAGAT ACCTTTGAAA GGATATCGCT TTCTTGTCTG TCTTTCGATA 300 TCATCATTAC AAGATGGAAT GCCTCCTCTG CATAAAGAAA TAACAATTCT CCTAGTATCT 360 TCAGTTTTTT AAAGAATAGA AGGATTGGTA CAATCACAAG TCTTTGAAAC AAATTTCCAG 420 TAGTTTTTCC AGGTATTGCT GGAAGATTTG GAAATAAAGA AGTAGCCCTT TAACCCAGTG 480 CAGGAAAATA GGCAAGCTTC ATCATCCTAT AAATGATCAT GCCCTCAGAA CTTGCTGCAA 540 CAGAAAAACC AGCTCTATCT ATGTACAGTA CTGAGAAAGT AGGGCCACTT CCTCTCACTT 600 GGGATCTGGG ATAGCTAACA CATGCCTAAA AGCAATCTGT TAAGTATGAC TGAAAGGGGA 660 CTGCAGATTA AAGTTGCAAG CTTCCAGCTT TGGGGTACCC AGGAGGGCAT CTCCTCCTGA 720 GGATCAACAA CAGAAAGAAA AAAGCAATGA ATCTGAGCAC AGCACATTCA AGTTTGTAAA 780 CTCTTTTCTA ACTTTCCACC TCAATGCCAC AGAGCAGTGC TACTGTGAAA CTGGGGACAA 840 AGAAGAGAAG GGCATCTGTA ATCGGGGAGC TCAGGGTGTG TGCAAAACGA TGATGATAAA 900 AAAAGGCAAG GAACAGCAGA ATATGCTGGA TTCAGCAGGA GCTGGGCCCC TGAGAGCTGG 960 GGAACTAACA GATTGCAGCC AAAGCTGCAG CCCTCACGTT TTCTGACTTG AGAGATAATG 1020 AAGCAATAAA AGCAGCAGAG GCAGCCAGTA AGGGCTCTGC TCCACAGGGT TGTCTGTGTG 1080 AGAGCAGCTG CTTGTGGGTG CCTGCTCAGA GTCCATCCAA GGACTGCAGG CCTCCAGCAG 1140 ACTAGCAAGG CAGAGGACCA AACAGCCAGG CCTCGGTGGC CCAGGGCTAA TTCCCTCCTT 1200 CAGAGACACC AGAACCTTGG CTCCCCAGCC TGTCACTGAG CCTGTCCCAG GGTGGGGCAG 1260 CCCATATGGT TGAGCTGTTG CATCGCCAGA GACACCAAGG GTAAATAAAC CCTGGGACTA 1320 CAGATGGGAG GCCAGCCAGG CTGGCTCCAC TTTTTGATCT CATCACGGGG GGCAGTCCGT 1380 GTGGAAACCC TGGGAGGCAC CTTAGCGATT TTCCAGGCCA ACAACTTCAT TTGTCAGATG 1440 AGAAAATCCC CCTCCCCCTC CTAGGGGTTA AGGGACTTGC CAAAAGTCAC ATAGTGAATC 1500 AATCGCAATG CAATAAAAAG TGGTGGCTGA GACCACAGCT GGGCTTGAGC TCCAGCTCTA 1560 TTGCTCTGGA GCTTGGGCAA GTTACATAGT TCTCAGTCTC TTCATCATAT AATGAGCGTA 1620 AGGTTAGGAC CTTCCATGTT AGGTTCTTGG GGAGATCAAA TGCATGAAAA GCCTATTGCC 1680 TGGTTCATAG TAACTGCTTA GTAAATATTG TTGGTTGGAA CTTATCGTCA 1730
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