Tag | Content |
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EnhancerAtlas ID | HS082-03326 |
Organism | Homo sapiens |
Tissue/cell | HCASMC |
Coordinate | chr1:228973770-228975220 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr1:228974358-228974369 | AGTGACTCATG | + | 6.14 | Gata4 | MA0482.1 | chr1:228974957-228974968 | TCTTATCTCCT | + | 6.14 | HNF1A | MA0046.2 | chr1:228973872-228973887 | TGTTAATCTTTAACC | - | 6.36 | HNF1B | MA0153.2 | chr1:228973873-228973886 | GTTAATCTTTAAC | - | 6.18 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_23450 | chr1:228971657-228975640 | Colon_Crypt_1 | SE_27943 | chr1:228970281-228975761 | Fetal_Intestine | SE_28861 | chr1:228970139-228975730 | Fetal_Intestine_Large | SE_52925 | chr1:228971171-228975530 | Small_Intestine |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I228834 | chr1 | 228970561 | 228975769 |
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Enhancer Sequence | CTTGTCATCC GGTGGGCACT GGGCCTGCCC CGCACAGCTC CTTCACCCCG GAGAGGTGAC 60 AGCAGACTAC ATTAGGCCCT GCCAGGCCCA AAGACTCCAG CCTGTTAATC TTTAACCAGA 120 GCTCTGGACA AAGGTAGCCC TTCTGACCTC CTGAGAGTTT CTGAATAGCT CGGAGGCTTC 180 TGTGACAGAG CCACACGTTA GCAATGACAT ATATTTAGTG CAGGGAGGCA TGTTGAGTAC 240 AGTTCTAAAT TCTGTTGTGA ATTGTGCCCA GGGAACAAGC ACAGAGAACA TTTTCACCAT 300 GGATATGTAT GTACTTGTAA GAAGCAGCTG GGTGGTTCCT TCAGCAATCT GCTGAGCTGT 360 GGCGATTACA TCACACACTG GTGCAAAGGC CTTGAACCAT TAATGTGCTG CCTCTGCGAG 420 GGTGACCAGG ATTCCAGCAA TGAACAGAGA AGGTGCTTGT CCCCACTGCT CACTGGGTGC 480 CTTCAGATTC TTAACTTTTG TCTTTTTCTT TTTTCTTTCA CTTCTTACCT GTATCTATAA 540 AACAGGACTC TGTTTGCTTT GAAAAGAGCC AGAATGACCT CAGGGGTCAG TGACTCATGC 600 TGTTGGCTCT GTGAACACAA TCGAGTGCCC CTTACGTAAG AAGCTCCTGC TATCTGAGGG 660 AAGGGAGGTC CGAGCCATTA TTCCTTGGTT ATAAACACTC CATGTGGTTT TGTTTGGTGG 720 TTTTAAAAAA GGTGTGTCCA CAGGGTTGGT GTTCTAGAAT CGTGGGCAGA AAGAAGTCTA 780 GCTCCTTTCA TCCAAGGTTC TAAAGGGTTC TCTGAGCTGT AACTCAGCTC TAACTGGACA 840 AAGAGGCAAC AATTCCCCTC ATTTCCTGTG CGCTGTCACC ACAGGAGGCT ACACTTAAGG 900 AGGTCAACTC AAGTTGTTTG GACCAAGCTT CCGCAGTTGT TCCCATTATC CTGTTTGAAT 960 CCATTCACTC TTACACTGGC CATGCAAATA GACACTCCCC AAGGAAAGAA GGACCTTAGA 1020 AAATAAGTGA TCTCAGTTTT CATCTGACTT TCTTCTGGGG TGTGGGGCTG GTCATGGGTC 1080 TATATTCCCT GCTGTGGTCA GGGCCCTGTG GGACATGTGG CTGTGTCCCA GCCCTCTAGC 1140 ACAATCTGCC GTCACTCCTG GGCTTTTGTA TGCCTGCTCC CATTTGCTCT TATCTCCTCA 1200 ACAACCACGT CAGGTAGATA ATACATACCA TCAGTCCCAG TTTACAGATG AAAAAAGTGA 1260 GGCACAGGGA GCTTCAGTAA CTTGATCAAG ACTAGAATTC AGAGAAATAG CCAAACCATG 1320 ACTCATGATC CTCTTGCTCC AAAGTGCGTT GTCTCCCCCA CAGCCCACTA TATTTGTTGT 1380 TTATTTTTGA AAATGGTCAT GAACTCAGCT AAGACGCTGG GGCAGTGGAG CGGAGGGAGA 1440 GAGCCTGCTC 1450
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