Tag | Content |
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EnhancerAtlas ID | HS047-22243 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr21:44896210-44897940 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EBF1 | MA0154.3 | chr21:44896616-44896630 | ACTCCCCTGGGAAT | + | 6.51 | ZNF263 | MA0528.1 | chr21:44896696-44896717 | TCCCATCTCTCTCCCTCCCCC | - | 6.24 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_24764 | chr21:44896104-44900163 | Colon_Crypt_3 | SE_34698 | chr21:44895700-44899975 | HeLa |
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| Number: 2 | ID | Chromosome | Start | End |
GH21I043476 | chr21 | 44896134 | 44900534 | GH21I006058 | chr21 | 44897243 | 44899840 |
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Enhancer Sequence | GAGGAAGGCA GAGAAGCCAT GGTGAAGACA TGAAGAGACA GCCACCTTCA CCCCTAACCC 60 TGTACCTGTG GGGTCAAGCA TGACATCTGA GCCTCTGTCC CTGGACTAGG GTAAACAAGG 120 GGATCTCTGG GCCCAGGAAG GCTGGGGGCA GGGGCTGTGA GGAGCTGAGG GGCCTGCAGG 180 CCACGCTGCC CTGGCACCCC ATCTGGCACC TCTAGGTGGG TTCCCTCTCA CTCCCGGTCA 240 GGGAGCAGCA TCTGACAAAA CACTCTGCTG CAGGCCTCGG TCTCCCCCTC TGCTGAACGT 300 CAGGCGGGTG CTGTCTGGGG CCTCCAGATG CTCCAAGGGG AAGACACGGC GCTGGAAGGC 360 TCTGGGCGGT GGAGGGCTGT ACAGGAGGGG CCATGGGCCT CCTGGAACTC CCCTGGGAAT 420 GCTAGAAGGG GGCAGAGACA GCTCAGATGA AGCCCTGAGA GATTCCAATG GCATCCCAGG 480 CCCCTCTCCC ATCTCTCTCC CTCCCCCATC ATCACTGCCT CTGAGGCCAG GGTACCCCAG 540 GCTCTCCAAC CCCACATATG GAGGCGGGCA GGCTCAGCTT CTGTCCAGCA CCAGAGCAGT 600 TGGAGAATGA AGTGGAACCC AAACGTGGCT CCGTCCCCCA GGGAGACAAA CCTGCAGACA 660 CCCTCCTGAG ACTGGGACAG GGGGACGGGG AAGCCTGGCC CAGACAGAAG CACGAATTGG 720 TGGCGTGGGC CTGGTGTTGA GAACAGGGTC CAACATCACA ACCCCGCTCG GGAGGCCAGC 780 GTCCGGGGCC TCTGCCAGCT CTGTCCCAGA CGGAATTTGT TCTCACTCTG GACACCCCCA 840 GGGGACCCCT GTGCTCACAG GCAGATCCAG GGGGCAGGAG GGGGGCCTTC CCATGCCAAG 900 TGCAGTTGGA TGATGAACGA CACCCCCAAA AGATTTGTCC AGGTCCTAAC CCGAGGAACT 960 GGAGAATGGG ACCTGATTTA GAAAAGGGGT CTTTGCAGAT AGATGGGATT AAGTTAAGGA 1020 TTTTGAGATG AAAGCCTCCT GGATGAGGGT GGACTTGAGA TCCAAGGACA CGTTCTGAGA 1080 AGGGGGAAAG GTGCAGAGAC ACAGTCACGT GAGACGGAGG CAGAGAACTG GAGCGATGCG 1140 GACACAAGCC AAGGACTGCC TGGGCCACCG GAAGCTAGGA GCGGCAGGAA GGGTTTTCTC 1200 CTGGAGCCTT CAGCAGGAGG TGGCCCTGCC GACACCTTGA TTTTGAAGTC TGGCCCCAGG 1260 ACTCAGAGAG TCCACTTCTG CTGCATGAGG CCCCCCGCAT GCAGTATCCT GTCATGGCAG 1320 CCCCTGCCTC ATGCGGCCTG GATCTCATGA GGGGTCCACT CCCCTCGTCT CCCCGGTGGG 1380 GCGCGGCATC TTCATGCTGC CCTCTAAGGA CAAGCGCATG AGAGGCCAGC CTCCCCCACC 1440 AGCAGGACAG AATGCACGAG GCCTTTACCA GGCCACACTG GCGCCTGGCG TGGCTAGGAC 1500 AGCAGTGCTG CTGCCCCGCT GTGGGGCCGA AAGAAGCCAG GGATGAGGGT GCGGGCGCAT 1560 CTGTGGGTCC CGGAGGCTCC AGACCCCCAG GCCAACTGCA CAGCCTGCAG GCAGCACTGC 1620 CTGGCCAGCC CTGTCATCCC TCTGTCCGTA CATCTAACCA CTTTCTCTCT GGGGCCGCCC 1680 CGCCCAGAGT CCCTTTCCTG CCGGAGGCTG GGGCTTTCCT GGCAGCTACT 1730
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