Tag | Content |
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EnhancerAtlas ID | HS101-28400 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr21:44896580-44897940 |
Target genes | Number: 15 | Name | Ensembl ID |
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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 | GGAGGGCTGT ACAGGAGGGG CCATGGGCCT CCTGGAACTC CCCTGGGAAT GCTAGAAGGG 60 GGCAGAGACA GCTCAGATGA AGCCCTGAGA GATTCCAATG GCATCCCAGG CCCCTCTCCC 120 ATCTCTCTCC CTCCCCCATC ATCACTGCCT CTGAGGCCAG GGTACCCCAG GCTCTCCAAC 180 CCCACATATG GAGGCGGGCA GGCTCAGCTT CTGTCCAGCA CCAGAGCAGT TGGAGAATGA 240 AGTGGAACCC AAACGTGGCT CCGTCCCCCA GGGAGACAAA CCTGCAGACA CCCTCCTGAG 300 ACTGGGACAG GGGGACGGGG AAGCCTGGCC CAGACAGAAG CACGAATTGG TGGCGTGGGC 360 CTGGTGTTGA GAACAGGGTC CAACATCACA ACCCCGCTCG GGAGGCCAGC GTCCGGGGCC 420 TCTGCCAGCT CTGTCCCAGA CGGAATTTGT TCTCACTCTG GACACCCCCA GGGGACCCCT 480 GTGCTCACAG GCAGATCCAG GGGGCAGGAG GGGGGCCTTC CCATGCCAAG TGCAGTTGGA 540 TGATGAACGA CACCCCCAAA AGATTTGTCC AGGTCCTAAC CCGAGGAACT GGAGAATGGG 600 ACCTGATTTA GAAAAGGGGT CTTTGCAGAT AGATGGGATT AAGTTAAGGA TTTTGAGATG 660 AAAGCCTCCT GGATGAGGGT GGACTTGAGA TCCAAGGACA CGTTCTGAGA AGGGGGAAAG 720 GTGCAGAGAC ACAGTCACGT GAGACGGAGG CAGAGAACTG GAGCGATGCG GACACAAGCC 780 AAGGACTGCC TGGGCCACCG GAAGCTAGGA GCGGCAGGAA GGGTTTTCTC CTGGAGCCTT 840 CAGCAGGAGG TGGCCCTGCC GACACCTTGA TTTTGAAGTC TGGCCCCAGG ACTCAGAGAG 900 TCCACTTCTG CTGCATGAGG CCCCCCGCAT GCAGTATCCT GTCATGGCAG CCCCTGCCTC 960 ATGCGGCCTG GATCTCATGA GGGGTCCACT CCCCTCGTCT CCCCGGTGGG GCGCGGCATC 1020 TTCATGCTGC CCTCTAAGGA CAAGCGCATG AGAGGCCAGC CTCCCCCACC AGCAGGACAG 1080 AATGCACGAG GCCTTTACCA GGCCACACTG GCGCCTGGCG TGGCTAGGAC AGCAGTGCTG 1140 CTGCCCCGCT GTGGGGCCGA AAGAAGCCAG GGATGAGGGT GCGGGCGCAT CTGTGGGTCC 1200 CGGAGGCTCC AGACCCCCAG GCCAACTGCA CAGCCTGCAG GCAGCACTGC CTGGCCAGCC 1260 CTGTCATCCC TCTGTCCGTA CATCTAACCA CTTTCTCTCT GGGGCCGCCC CGCCCAGAGT 1320 CCCTTTCCTG CCGGAGGCTG GGGCTTTCCT GGCAGCTACT 1360
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