Tag | Content |
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EnhancerAtlas ID | HS094-36559 |
Organism | Homo sapiens |
Tissue/cell | hMADS-3 |
Coordinate | chr6:126374730-126376590 |
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) |
E2F6 | MA0471.1 | chr6:126375053-126375064 | GGGCGGGAAGG | + | 6.62 | INSM1 | MA0155.1 | chr6:126375040-126375052 | TGTCAGGGGGTG | + | 6.22 | ZNF263 | MA0528.1 | chr6:126375047-126375068 | GGGTGAGGGCGGGAAGGGGGA | + | 6.46 | Znf423 | MA0116.1 | chr6:126375526-126375541 | GCCCCCCTAGGTGCC | - | 7.52 |
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| Number: 1 | ID | Chromosome | Start | End |
GH06I126054 | chr6 | 126375237 | 126375750 |
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Enhancer Sequence | CCTGCCTTAC CTGTTCCTTC CTCTGGAAAC CACAATAAAG GCTCTTGTCC ACATTTTCCC 60 CTCCCCTCTG CCTCCTGAAC GACCCTGGTC CTTCCCCACA TGGCCCTGCA TGGCGTGGTG 120 TGTCCTCTCG AGAGCTTCGA GGAACAAACT GTCTTTTCAA TTAAAATTGT CTTGTGATCT 180 GTTGGTCTCA CCATACCTGA ATAATAATAA AACCTACATT TAAAAACACG TGAGAGAGGA 240 CTGGATCAAG GAAGAAGCCT GAGAGATGAC ATCTAAGTTA ACCCCTAAAG AAGTGGAAGT 300 TGCGTGATCA TGTCAGGGGG TGAGGGCGGG AAGGGGGATT CCAGGCAGAG AGAATAGCAC 360 TGGAAAAGCA TATTTGGGTA ACAGTTCAAC TAGTTGGTGT GCCAGGAGCT AAATGCATTA 420 GCCAAAGAGG AGAAATGAAG CTGGACAGGT CATGAGAGCC AGATCCTAAA GGACTCATAC 480 GCCCTGCTGC AGAATCTGCA CTTAATTCTG GGAGAAGCCC ACTCCCTGTG ACCTCCTCTC 540 CCCTTTGGTA ATGCCAAGGC TCTTTGGGAA GTTTTAATTT CTTTCAAAAT GGTGTCCTTG 600 GCTGAAGTGC TTGAGTTCCT TGACAAAGGG TGCCTGTAAA GAGGGAGTCT GTGGCTTTGC 660 CTTTGCTCCA GGGTCTGTTT CTGCCTTGGT TCTAGGTCTC AGTTAATGCT GTCTTCTAAG 720 TTGGGTGAAT TGCATAGCTG AGGCTGCTTG AATTAAGGCA TTGACACCAC AAAGCTTCCA 780 TTTCCCCATC TATAGAGCCC CCCTAGGTGC CCAGTTACAC TGTGGTAAGA GATTGCCCAG 840 ATAAGTACAG TAGAAACCTT CCTGACCCTG ACTGACAGAT ACTTGCTCCA GAGCCAAGAA 900 ACAGTCACAT GTTGGCCTCC TGCACCGAGG GAGATGATTT TTATTGATTT CGCTCTTCAC 960 ACAGTGCTGA CGGTGTAGGC CTGCTGAAGA GCAAGCTGAT GAAAATAAAG ATTGTGGGTT 1020 GCCAGCTCAT GTTTGTCCTT ATCTCCAAGG CAAAATACAA ACACTGTTTC AGGGAGCTGC 1080 TTCTCCGCTC CAAGACAAAT GAGCTGTTGA AGTGTCATGA TTTTAAAATC TGGTGATATA 1140 CATAAAGGAT ATTTTACTGA TCAACCTCAA GGAATCTGTC ATAAATAAAA AATAGTTTGT 1200 GATTCAAGCA CTGTTGCCTA TTTCAGAACT TCACCTTGGA GCCCACTCTG CTGTCTTCTG 1260 AGACACAGGG TGCTCCCTGA AAGAAAACAG CTCAGAACTC CCAACACGTC TCTTTCGCAT 1320 CTTTCCTTGA AGATTCTTAC CAAGAGCAAC CAGGCTTTTT GAGTCACCAT ATGCTGACGA 1380 ACATTTTTGT TGTTTTTTGA GACAGGGTCT GGCTCTATAG CCCAGGTTGT AGTGTAGTGG 1440 TGCAGTCTTA GCTCACTGCA GCCACAACTT CCTGGGTTTA AGCAATCCTC CCGCCTCAAC 1500 CTCCTGAGAA GCTGGGACTA CAGGCACATG GCACTTCACT CATCTAAGTT TTATATGTTT 1560 TGTAGAGACA GGGTTTCTCC ATGTTGTCCA GGCTGGTCTT GAACTCTTGG GCTGAACTGA 1620 TCCCCTTGCC TCGGCCTCCC AAAGTGCTAT GATTACAGGC ATGAGCCACT GTGCCTGGCC 1680 TTTACGACCT TTTAAAAACC CATTACTAAT GAGGATGAGA GGAAGGACAG CATGGAATCC 1740 TCTAGCCCTT GCTTGTGGCC CGCCTGGTTT TCTCTAACAC TCCCTGCCTG CTTCTCCTTC 1800 ACTATTTACT GCATGCCTGG CATATGCCAG CCAGCAACCA CTATGAACAT CAGATGAATA 1860
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