Tag | Content |
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EnhancerAtlas ID | HS129-01758 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr1:118155150-118156030 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFE2L1 | MA0089.2 | chr1:118155616-118155631 | TAAGCTGAGTCATTC | - | 6.29 | Nfe2l2 | MA0150.2 | chr1:118155618-118155633 | AGCTGAGTCATTCTT | - | 6.2 |
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| Number of super-enhancer constituents: 12 | ID | Coordinate | Tissue/cell |
SE_11059 | chr1:118146523-118172865 | CD20 | SE_12835 | chr1:118155573-118155727 | CD34_fetal | SE_12835 | chr1:118155744-118155937 | CD34_fetal | SE_15163 | chr1:118153670-118158216 | CD4_Memory_Primary_7pool | SE_21364 | chr1:118154830-118158002 | CD8_Memory_7pool | SE_31627 | chr1:118155085-118157819 | Gastric | SE_43509 | chr1:118148646-118179652 | MM1S | SE_61007 | chr1:118138819-118218057 | HBL1 | SE_62427 | chr1:118147317-118217904 | Tonsil | SE_65708 | chr1:118155677-118157095 | Pancreatic_islets | SE_66608 | chr1:118154437-118162016 | Jurkat | SE_67143 | chr1:118148646-118179652 | MM1S |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I117611 | chr1 | 118154582 | 118158622 |
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Enhancer Sequence | AAGTGTTTGA GCTGTCTGGT GACAGCACAT TAATTACTTG ATGAACGCTA AACATGAGCT 60 GCTGCTATGC GCAGTACCTG GAGGCCCGGA ACCTGCAACT TGAATGCCAA CTCCTAAGGG 120 AAGGATCCAT GCAAAACAAA AACCTGGATG GAACTATGCA CGTAATTAGC ATCTGCTCTG 180 AAATGGAGGT CAGCTCACAC TTAGACACTT GTGAATGGGG TGTGTTTATG GTCTAACGTA 240 TGATAAGGGT GGCATTTGAG GAACTAAGAG TTGCTTGTCC CTTTCCTGAT AAGGCCTGGG 300 CAGGGAAGCT GCTAGTGATT AGACAGGACT TTTAGCTGAC TGAGGTCTTC CTTTTGGACA 360 ACTGTTTAAA GCTGTAGGCT GGAGAGTTAG ATGGTAAAGT AGCCTGTGGA AGCAGCCTTT 420 GATGAAACCC GGAGGCTGTC AGCTCTTAAA CCCTGTGGAT TACGTGTAAG CTGAGTCATT 480 CTTACAGTAA GCAGTCTCCT CCTTAGGAAT CATCTCATTT TTCTCAGTCT GGGCAATCTC 540 TAAAACAGAA AGGCAGGCTC TCTTTGGGGA GCTCTTTAAA TGAATTCAGA CCAGTAACAC 600 CTCTGATCTA GAAAGAAGCA GTTGATGGTG GGAAGGTGGT TACCAAGTAG CAACAAGGAT 660 TATTTCCATT TCAAGTTGTG TGTGTAGCAC TTAATGCTGA CACCTTGGAA AAAAATCAAG 720 GCTTTTATGC CCTGCTTCCA TCTGAAGATG TCTGTGTCCT GACCTTGTTA ATATTTCCAT 780 TTGCAACCAC GTCAGAGTAT ACCTTTCAAC ACTTGAACTT GTGTGGCATC CCTGCTGTAA 840 TATCTAGGCC AGTGTTTTGA TTCTGTTTGC TGTTTTGCGG 880
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