Tag | Content |
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EnhancerAtlas ID | HS129-01126 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr1:51779510-51780960 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOS | MA0476.1 | chr1:51779722-51779733 | TGTGACTCATC | + | 6.14 | JUND | MA0491.1 | chr1:51779722-51779733 | TGTGACTCATC | + | 6.14 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_24436 | chr1:51779529-51780130 | Colon_Crypt_2 | SE_24436 | chr1:51780154-51781404 | Colon_Crypt_2 | SE_65473 | chr1:51777645-51782962 | Pancreatic_islets |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I051313 | chr1 | 51778781 | 51781505 |
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Enhancer Sequence | GTAATAATAA TTTTTTTAAA AAAGAAAGAA ATGCTCTTCC TCTACATCTC CTGACATATC 60 TGTCAAGGCC TCAAATGCCT CCCAGACCAC TGGGAATCCA GGCCTCCTCC TCAGGGACTC 120 CATCTGTAAC TGAGGCACGG GCCACGCTGA ACTGACATCA GCATAGGCTC AGCTCTCCCC 180 ATACTGTGGG CACCTCGAGG ACAGAGCTTG TGTGTGACTC ATCTCTGTCC TCAGCACCGA 240 TGTCAGGGCT GAGCCAAGGT GGCCTCAGGA GCCTCTGGGC TCCCTGCTCC TTCACCGACC 300 CAGGCTCCTC AGCTGAAGGG TGTGTTGGGG GCAGGGGGTG GCATTTAGTC CATCACATGG 360 AGAAGGCAAC AGGCAGGGAG GGACGGGAAC AATGCCAGGT CCTCTCTGTA TGTGGAGGGA 420 GTCACTTAAC ATGTCTGGGC CTAGATTTCT GCTTCTGCAA AATGGGGACG ATAATGCCAG 480 CCTGCCCGGG TCCCTGCGAG ACTGTGGGAC TGACTGAGAG CGCCTTTACT CCCTTCCCCA 540 GGTCTCCTCG TGAATTATTT ATGAATCTCC TCAGTGCCAG GTTTATGCTG GGAACTTCAG 600 AGGAAAGAGA GATGACTAAG GTTTACAGGC TGTTTGGTTG TGAAATCATG TGACTTTACC 660 CCTTTTCCTG CTTTTCCTGT TCATAAAACA CTCATAAGTT AAGTTACTTC TGGGTGACAC 720 TCCTGTGATC CTTGAGGGTC AAAGGAAGGA AACCAAGGCT GCTCTACCAC TCGCCAGCCA 780 GGGGCACTCT CTGGATGCTC CCAGGCCTTT GCTAGGACTG CTTAATCTGC AGGCAGTGGC 840 TTGTAGAGAG GAGCAGGCTG CCCAGAGTGG GGGCCAGAAC CAGGTTTCAG AGTCCCTCAG 900 ACACAGGTTG GAGTCAGCTT TGCCAGCTAC CAGCTGTGTG ACCTGGCATG TCTCATGTCT 960 CATAGCCTCT CTGAGCCTCA AGTTTTTCCC TGCGGAAGGA AAACCTTAAC TCTTCTCCCC 1020 AATGGGTTTT TGCATGGCTT AAATAGAATA CCCAGGCCAG GGGCCACTGC ACCAAAGCTC 1080 GGTAAATATG AGTCCCTCCG TGTCCTGCGT CACTTCCCTG CATAAAGTCC TTCTCCTCGA 1140 GGAGGGGCTT CCCTGGCAGC ACACAGACCC ATCCCCCAGA TAACACCCCC AGCCCCCAGG 1200 CCTCTCCATC TCTCAAGTCC TTGTCTCTCT CTTCCTCTCC CACTGCAGGT CTGAGGCCCG 1260 GGACTCAGCA CCACCTGCCC AGCCCCACCT GTGGAAACTT GTCTGGTGCT GGGCCCAGAA 1320 AGAGGGACAG CCCCACCCGG GCAGCTGGCA GAAATGTGGA ATTTCTAGTC TGAGGCCCAA 1380 GGCCCCAACA GGCACCTGTG GCTAAGAATA CTAGCCCCTC CCCAGCCTAC CTCCTGGAAG 1440 CCCCCAACTC 1450
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