Tag | Content |
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EnhancerAtlas ID | HS074-01382 |
Organism | Homo sapiens |
Tissue/cell | GM19239 |
Coordinate | chr1:228972800-228974910 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr1:228974358-228974369 | AGTGACTCATG | + | 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 | AATTGCTTGG TTTTGTATTT TCATTTCTTT TCCTGACTGA AAATGGATCT GGAGCCTGAG 60 AGCACCTGAT GTTGGGCGAG GCCTCTGGGT ACGAGGTGGA AGTTCACATT TCTGGATTAT 120 GTGTAGTTTC AGAATGCCTT CTATCTCGGT GTCAGGATAG ATGTTAAGAT GCAGGAATTC 180 TCATAAATCT TCTCGTTAAA AAGAAGAAAA CAACAAAACT TCTCACAGAA CATAAAAACC 240 ATGTCAGGTG GCCGGGCGTG GTGGCTCATG CCTGTAAACT CAGCACTTTG GAAGTCCAAG 300 GTGGGTGGAT CACGAGGTCA GGTATTTGAG ACCAGCCTGG GCAACATGTG AAATCCCGTC 360 CCTACTAAAA ATACAAAAAT TAGCGGGGAG TTGTGGCACA CTCCTGTAAT CCCAGCTACT 420 CAGGAGGCTG AGGCAGGAGA ATCGCTTGAA CCCAGGAGGC AGAGGTTGCA GTGAGCCAAG 480 ATCATGCCAT TGCACTCCAG TCTGGGCGAC AGAGCAAGAC TGTCTCAAAA AAAACCCCAA 540 AAAAACAAAA AAAACCCATG TCAGGTTGCT CCCCTGAGCA AGGCCAAGCT CAGTTTTCAC 600 CTGGTGGTCC CATGGGGAGC TTCCTGTGGC TTAGTGTTTG CGTCTGCCAT TTGCTATCCC 660 TCCCCAGCAC ACCTTCCTGT GGATGGAACT TGCCAGAACT TCCTCAGCAA CCCTGAAGAG 720 GAAAGCTGGA GGCCCCAACA GACGCAGAAG TGGGCTGCAC TGCTGTGCTT CCATGGGGCA 780 GTCAGGGCTC AGGGCCCCAG CAGCAGGCCA AACCCCAGCC CAGCTCCCTT GCAAACCTCC 840 TCTGTCATGT ACCCTGGGAG TCAGGTCCAA CCCCACTATG TCACAACTGA GGAAACAGAG 900 GCCCCGAGAA GTTCAGGGAG AGCTGGGGTC AAGATGCTAG ATCCTGCCTC TGGGTGTGGT 960 GGCTTTTGTT CTTGTCATCC GGTGGGCACT GGGCCTGCCC CGCACAGCTC CTTCACCCCG 1020 GAGAGGTGAC AGCAGACTAC ATTAGGCCCT GCCAGGCCCA AAGACTCCAG CCTGTTAATC 1080 TTTAACCAGA GCTCTGGACA AAGGTAGCCC TTCTGACCTC CTGAGAGTTT CTGAATAGCT 1140 CGGAGGCTTC TGTGACAGAG CCACACGTTA GCAATGACAT ATATTTAGTG CAGGGAGGCA 1200 TGTTGAGTAC AGTTCTAAAT TCTGTTGTGA ATTGTGCCCA GGGAACAAGC ACAGAGAACA 1260 TTTTCACCAT GGATATGTAT GTACTTGTAA GAAGCAGCTG GGTGGTTCCT TCAGCAATCT 1320 GCTGAGCTGT GGCGATTACA TCACACACTG GTGCAAAGGC CTTGAACCAT TAATGTGCTG 1380 CCTCTGCGAG GGTGACCAGG ATTCCAGCAA TGAACAGAGA AGGTGCTTGT CCCCACTGCT 1440 CACTGGGTGC CTTCAGATTC TTAACTTTTG TCTTTTTCTT TTTTCTTTCA CTTCTTACCT 1500 GTATCTATAA AACAGGACTC TGTTTGCTTT GAAAAGAGCC AGAATGACCT CAGGGGTCAG 1560 TGACTCATGC TGTTGGCTCT GTGAACACAA TCGAGTGCCC CTTACGTAAG AAGCTCCTGC 1620 TATCTGAGGG AAGGGAGGTC CGAGCCATTA TTCCTTGGTT ATAAACACTC CATGTGGTTT 1680 TGTTTGGTGG TTTTAAAAAA GGTGTGTCCA CAGGGTTGGT GTTCTAGAAT CGTGGGCAGA 1740 AAGAAGTCTA GCTCCTTTCA TCCAAGGTTC TAAAGGGTTC TCTGAGCTGT AACTCAGCTC 1800 TAACTGGACA AAGAGGCAAC AATTCCCCTC ATTTCCTGTG CGCTGTCACC ACAGGAGGCT 1860 ACACTTAAGG AGGTCAACTC AAGTTGTTTG GACCAAGCTT CCGCAGTTGT TCCCATTATC 1920 CTGTTTGAAT CCATTCACTC TTACACTGGC CATGCAAATA GACACTCCCC AAGGAAAGAA 1980 GGACCTTAGA AAATAAGTGA TCTCAGTTTT CATCTGACTT TCTTCTGGGG TGTGGGGCTG 2040 GTCATGGGTC TATATTCCCT GCTGTGGTCA GGGCCCTGTG GGACATGTGG CTGTGTCCCA 2100 GCCCTCTAGC 2110
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