Tag | Content |
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EnhancerAtlas ID | HS083-00044 |
Organism | Homo sapiens |
Tissue/cell | HCC1954 |
Coordinate | chr1:24616070-24617490 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CDX2 | MA0465.1 | chr1:24616454-24616465 | AAGCAATAAAA | + | 6.32 | ZNF263 | MA0528.1 | chr1:24617148-24617169 | GGAGGAAGAGAGGAAAAAGAA | + | 6.5 | ZNF263 | MA0528.1 | chr1:24617141-24617162 | GAAGCAGGGAGGAAGAGAGGA | + | 6.74 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_26668 | chr1:24615522-24618794 | Esophagus | SE_35109 | chr1:24616022-24618226 | HeLa | SE_64493 | chr1:24616030-24617222 | NHEK |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I024289 | chr1 | 24616197 | 24617447 |
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Enhancer Sequence | GCAACATAGC AATATCCCCT CTCTAGAAAA AAAAAGTTTT AAACATTAGC TGGGTGTGGT 60 GGTGTATGTC TGTAGTTCCA GCTACTTGGG AAGCTGAGGC AGGAGGATCA CTTGAGCTTG 120 GGAGCTGGAG GCTGCAGTGA ATCATGATCA TACTGGTGAC ACAGTGAGAC CCTGTCTCAT 180 AAAAACAAAA AACAAAAAAG TGCATTGTTA CTATTATCAT CATTGGCCCA GGACCCTGTG 240 TTCTATACAC AGGGTGATTT TAACCAAGGT TTAGAGAAGG CCTGTCTGCA CCAGAACTCC 300 GGGCTGGCAT CATTTTCATA AATTCTTTGT CCCATTCAGC TCCTCTCTGG CTATTCAGAA 360 AATAATCTGA ATGTTGAAAC TTGTAAGCAA TAAAAGGATT TCATGACACA GGCCAAATCA 420 GGACTTTTCC GCTTTGCAAT GACAGCCTTC CCCTCTCCTC TGCTGTGGCC CTGGCTCTCC 480 ACTCTCTCCT TGGGCTTCCC ATGGGACTGC TTAGCATGGA TCCCACGGGG TTATGGTTAA 540 CAGTCAAGAG TCCCGGGCGC AGGGCCAGGA TGGCAACTCG CCCAGGGCAG GAAGCAGCTT 600 ACGCATCAGT ATTCCCCATA CTCAGCACAG GGCCTGGCAC AGATCAGTGC CCTGTGAAGG 660 GCTATGAGTT GAAAAAATAG TGACCTAGAG TGTACTGGGT GTCTCACCCA AACTTCCCTG 720 ACACGGAATA GAAAGCGATG AACAGAGTTA GCACTCAATA TGTATTTGTG GGCCGGGCGT 780 GGTGGTTCAC GCTTGTAATC CCAGCACTTT GGGAGGCTGA GGCGGGTGGA TTGCTCGAGG 840 TCGGGAGTTT AAGACCAGCA GGGCCAGCAT GATGAAACTC TACTGAAAAA AAAAACAAAA 900 ATTAGCCAAG CGTGGTGGTA GGTGCCTATA ATCCCAGCTA CTGGGGAGGC TGAGGCATGA 960 GAATCTCTTG AACACATGAG GTGGAGGTTG CAGTGAGCCA AGATTGTGCA CTGCACTCCA 1020 CCATGGGTGA CAGACCGAGA CTCCATGTCA AAAAAAAAAA AAGTATTTGT GGAAGCAGGG 1080 AGGAAGAGAG GAAAAAGAAG GAAAGAAGAG GCATGCCTGA CCCACCAACT GGATGACCAA 1140 ACTATGAAAG AACCGAGAAA CGAATGAAAT GGAATTCCTC TCGTAGTTCT CCTTCTCTGG 1200 AGAACTCTCC TTCTCATCAT TGGAAAAGGA GATAAATTAA ATGAGTTGGT CTTTTAAATA 1260 ATAAGCGCTA GCATAATAGC CGTATTTACC ATGTGACCAG CTGTGTTCTG TTCATTTTGA 1320 GTGTATTAAC TAATTTAATT CTCACACCAA TTCTAGGAGA TGTGTTACTG TGCCCATTTT 1380 ACAAATGAGC AGACCAAGGC TCCAAGAAGC CAAGTAACAA 1420
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