Tag | Content |
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EnhancerAtlas ID | HS043-06737 |
Organism | Homo sapiens |
Tissue/cell | Fetal_heart |
Coordinate | chr10:122838360-122840590 |
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 | CCCCTTCGCA CATTCCTGGG CTTAGATCCA CATTCCCTGG GTCTTCATCA TTCCAGACGC 60 AAAGACCTGA TCTGTCTTGC CTGCCAGTGC TCACCCCACA CCTTGACAAC CTCTCCATCA 120 TTTTCATTCC TTTTGCTGGC CCTGCTCCAG GACCTCTGAG GCTTGAGAAG CAGCAAGCTG 180 ATTCACCCCG TCCCGTCTAG GCGTGGCCCC TCACACCCTG CCCAGGGAGC AGGCTAGTTC 240 AGCTGCTTTG AAGGATGCTG CCTGCTTCTC TCCTCCTCAC TGCCCTCTCA GGTCCAGCCT 300 CATACAGCCT CATACAGCCT CGGAGTCAGC CGTTTCAAGT GATTTCCAAG AATCATCATT 360 GGAAAAAAGC CTTGTAACCA TCAAGTGGTG CTGATCTAAT AAGAGCCAGC ACAAATCCTA 420 CGTTAAACTA AGCAAATGGC GTTAATCTCA TCATCATCAT CAAGCCTAGG CCCACAGCCT 480 GAGGTGACAT GGGGTGACCG AGTCTCTGGA TTGTGTGAAG GAAGGCTCCA GTGATCAGGT 540 TGCTGCAAGA TCAGGTTGAC TTGGGGTAAT AACCGCAGTT GCAATTACAT GTGCTGTTTA 600 CATACTTTGC CCCTTGTACT TGATAAAGTC CAGAAAGAGC CCTGGGCGCA GCTGCTCAGC 660 GCCTCTTGGG GGTAAGCCAC ATACCCTGTG GGAGCAGGAG AGCCACCTCT CCCCTGAGAG 720 AGAAATAGGG CCCAGATAAT GTCTAGTTTA GGTACCTCTT CAGACCAGAT ACCTTTGAAA 780 GGATATCGCT TTCTTGTCTG TCTTTCGATA TCATCATTAC AAGATGGAAT GCCTCCTCTG 840 CATAAAGAAA TAACAATTCT CCTAGTATCT TCAGTTTTTT AAAGAATAGA AGGATTGGTA 900 CAATCACAAG TCTTTGAAAC AAATTTCCAG TAGTTTTTCC AGGTATTGCT GGAAGATTTG 960 GAAATAAAGA AGTAGCCCTT TAACCCAGTG CAGGAAAATA GGCAAGCTTC ATCATCCTAT 1020 AAATGATCAT GCCCTCAGAA CTTGCTGCAA CAGAAAAACC AGCTCTATCT ATGTACAGTA 1080 CTGAGAAAGT AGGGCCACTT CCTCTCACTT GGGATCTGGG ATAGCTAACA CATGCCTAAA 1140 AGCAATCTGT TAAGTATGAC TGAAAGGGGA CTGCAGATTA AAGTTGCAAG CTTCCAGCTT 1200 TGGGGTACCC AGGAGGGCAT CTCCTCCTGA GGATCAACAA CAGAAAGAAA AAAGCAATGA 1260 ATCTGAGCAC AGCACATTCA AGTTTGTAAA CTCTTTTCTA ACTTTCCACC TCAATGCCAC 1320 AGAGCAGTGC TACTGTGAAA CTGGGGACAA AGAAGAGAAG GGCATCTGTA ATCGGGGAGC 1380 TCAGGGTGTG TGCAAAACGA TGATGATAAA AAAAGGCAAG GAACAGCAGA ATATGCTGGA 1440 TTCAGCAGGA GCTGGGCCCC TGAGAGCTGG GGAACTAACA GATTGCAGCC AAAGCTGCAG 1500 CCCTCACGTT TTCTGACTTG AGAGATAATG AAGCAATAAA AGCAGCAGAG GCAGCCAGTA 1560 AGGGCTCTGC TCCACAGGGT TGTCTGTGTG AGAGCAGCTG CTTGTGGGTG CCTGCTCAGA 1620 GTCCATCCAA GGACTGCAGG CCTCCAGCAG ACTAGCAAGG CAGAGGACCA AACAGCCAGG 1680 CCTCGGTGGC CCAGGGCTAA TTCCCTCCTT CAGAGACACC AGAACCTTGG CTCCCCAGCC 1740 TGTCACTGAG CCTGTCCCAG GGTGGGGCAG CCCATATGGT TGAGCTGTTG CATCGCCAGA 1800 GACACCAAGG GTAAATAAAC CCTGGGACTA CAGATGGGAG GCCAGCCAGG CTGGCTCCAC 1860 TTTTTGATCT CATCACGGGG GGCAGTCCGT GTGGAAACCC TGGGAGGCAC CTTAGCGATT 1920 TTCCAGGCCA ACAACTTCAT TTGTCAGATG AGAAAATCCC CCTCCCCCTC CTAGGGGTTA 1980 AGGGACTTGC CAAAAGTCAC ATAGTGAATC AATCGCAATG CAATAAAAAG TGGTGGCTGA 2040 GACCACAGCT GGGCTTGAGC TCCAGCTCTA TTGCTCTGGA GCTTGGGCAA GTTACATAGT 2100 TCTCAGTCTC TTCATCATAT AATGAGCGTA AGGTTAGGAC CTTCCATGTT AGGTTCTTGG 2160 GGAGATCAAA TGCATGAAAA GCCTATTGCC TGGTTCATAG TAACTGCTTA GTAAATATTG 2220 TTGGTTGGAA 2230
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