Tag | Content |
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EnhancerAtlas ID | HS182-02034 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr1:228973200-228975560 |
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 | CTCCTGTAAT CCCAGCTACT CAGGAGGCTG AGGCAGGAGA ATCGCTTGAA CCCAGGAGGC 60 AGAGGTTGCA GTGAGCCAAG ATCATGCCAT TGCACTCCAG TCTGGGCGAC AGAGCAAGAC 120 TGTCTCAAAA AAAACCCCAA AAAAACAAAA AAAACCCATG TCAGGTTGCT CCCCTGAGCA 180 AGGCCAAGCT CAGTTTTCAC CTGGTGGTCC CATGGGGAGC TTCCTGTGGC TTAGTGTTTG 240 CGTCTGCCAT TTGCTATCCC TCCCCAGCAC ACCTTCCTGT GGATGGAACT TGCCAGAACT 300 TCCTCAGCAA CCCTGAAGAG GAAAGCTGGA GGCCCCAACA GACGCAGAAG TGGGCTGCAC 360 TGCTGTGCTT CCATGGGGCA GTCAGGGCTC AGGGCCCCAG CAGCAGGCCA AACCCCAGCC 420 CAGCTCCCTT GCAAACCTCC TCTGTCATGT ACCCTGGGAG TCAGGTCCAA CCCCACTATG 480 TCACAACTGA GGAAACAGAG GCCCCGAGAA GTTCAGGGAG AGCTGGGGTC AAGATGCTAG 540 ATCCTGCCTC TGGGTGTGGT GGCTTTTGTT CTTGTCATCC GGTGGGCACT GGGCCTGCCC 600 CGCACAGCTC CTTCACCCCG GAGAGGTGAC AGCAGACTAC ATTAGGCCCT GCCAGGCCCA 660 AAGACTCCAG CCTGTTAATC TTTAACCAGA GCTCTGGACA AAGGTAGCCC TTCTGACCTC 720 CTGAGAGTTT CTGAATAGCT CGGAGGCTTC TGTGACAGAG CCACACGTTA GCAATGACAT 780 ATATTTAGTG CAGGGAGGCA TGTTGAGTAC AGTTCTAAAT TCTGTTGTGA ATTGTGCCCA 840 GGGAACAAGC ACAGAGAACA TTTTCACCAT GGATATGTAT GTACTTGTAA GAAGCAGCTG 900 GGTGGTTCCT TCAGCAATCT GCTGAGCTGT GGCGATTACA TCACACACTG GTGCAAAGGC 960 CTTGAACCAT TAATGTGCTG CCTCTGCGAG GGTGACCAGG ATTCCAGCAA TGAACAGAGA 1020 AGGTGCTTGT CCCCACTGCT CACTGGGTGC CTTCAGATTC TTAACTTTTG TCTTTTTCTT 1080 TTTTCTTTCA CTTCTTACCT GTATCTATAA AACAGGACTC TGTTTGCTTT GAAAAGAGCC 1140 AGAATGACCT CAGGGGTCAG TGACTCATGC TGTTGGCTCT GTGAACACAA TCGAGTGCCC 1200 CTTACGTAAG AAGCTCCTGC TATCTGAGGG AAGGGAGGTC CGAGCCATTA TTCCTTGGTT 1260 ATAAACACTC CATGTGGTTT TGTTTGGTGG TTTTAAAAAA GGTGTGTCCA CAGGGTTGGT 1320 GTTCTAGAAT CGTGGGCAGA AAGAAGTCTA GCTCCTTTCA TCCAAGGTTC TAAAGGGTTC 1380 TCTGAGCTGT AACTCAGCTC TAACTGGACA AAGAGGCAAC AATTCCCCTC ATTTCCTGTG 1440 CGCTGTCACC ACAGGAGGCT ACACTTAAGG AGGTCAACTC AAGTTGTTTG GACCAAGCTT 1500 CCGCAGTTGT TCCCATTATC CTGTTTGAAT CCATTCACTC TTACACTGGC CATGCAAATA 1560 GACACTCCCC AAGGAAAGAA GGACCTTAGA AAATAAGTGA TCTCAGTTTT CATCTGACTT 1620 TCTTCTGGGG TGTGGGGCTG GTCATGGGTC TATATTCCCT GCTGTGGTCA GGGCCCTGTG 1680 GGACATGTGG CTGTGTCCCA GCCCTCTAGC ACAATCTGCC GTCACTCCTG GGCTTTTGTA 1740 TGCCTGCTCC CATTTGCTCT TATCTCCTCA ACAACCACGT CAGGTAGATA ATACATACCA 1800 TCAGTCCCAG TTTACAGATG AAAAAAGTGA GGCACAGGGA GCTTCAGTAA CTTGATCAAG 1860 ACTAGAATTC AGAGAAATAG CCAAACCATG ACTCATGATC CTCTTGCTCC AAAGTGCGTT 1920 GTCTCCCCCA CAGCCCACTA TATTTGTTGT TTATTTTTGA AAATGGTCAT GAACTCAGCT 1980 AAGACGCTGG GGCAGTGGAG CGGAGGGAGA GAGCCTGCTC TTCACAGAGG GCTTATGGGG 2040 TGAGAGGAAG GGAAGCTAAG TACAGGGCAG GCCGGGGCCA TCTAAGGTGG CCTCTGACCA 2100 TCCTGGAGAG GCATGGGGCT AGAGAATGAA GAATGAGGCA GAAATGAGCG TTTTTGAACT 2160 GGTTTACCGA GCAAGAACTA GAATGGAAGG GGACATATTA CAAATGACAA ATGCCTGATC 2220 CAAAGCCCAT GAGATGCTAT TGATGAGGGC CACGGACCCT TACTCTGTGC AGACACAGAG 2280 GCTTGGATGC ACACACTTGC ATACACACAC ACACACACAC ACGCACTGTT TTGTTTTGCT 2340 CTGCTTTATT TTTGCCACTG 2360
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