Tag | Content |
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EnhancerAtlas ID | HS184-24118 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr5:66510680-66512240 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESR1 | MA0112.3 | chr5:66511107-66511124 | TAGGTAACTGTGACCTG | + | 6.14 | PPARG | MA0066.1 | chr5:66511106-66511126 | TTAGGTAACTGTGACCTGTT | + | 6.01 |
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| Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
SE_09678 | chr5:66510668-66513068 | CD14 | SE_10334 | chr5:66510576-66514036 | CD19_Primary | SE_10981 | chr5:66510129-66514936 | CD20 | SE_43394 | chr5:66509553-66515196 | MCF-7 | SE_58543 | chr5:66482007-66542810 | Ly1 | SE_59619 | chr5:66423406-66518818 | Ly4 | SE_60797 | chr5:66482600-66512719 | DHL6 | SE_61350 | chr5:66477635-66518960 | HBL1 | SE_61690 | chr5:66482564-66519078 | Toledo | SE_62454 | chr5:66477233-66519293 | Tonsil |
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| Number: 1 | ID | Chromosome | Start | End |
GH05I067214 | chr5 | 66510650 | 66514479 |
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Enhancer Sequence | AACAGCGCTG AACTTTCCAG ACAGCTGCAT GGAGTTGTCA TCCATCCTTC TCTGGAGAGT 60 GTCTGATCCC TTCTCTAAAC TTATGCCCTG CTCCTCTCCC CTATCTGTGC ACAGAGGACT 120 TGGTCCGATT CTACCTCCGG AACAATGCTC AGCCCACAGC CCTCATTCCC TCCGTGATGA 180 ACAGTAACTG TGGACTTTTG ACCTTCCTCT TGAGCTTGGT CTGAGTCTTG GCATTTACAA 240 CCACGGCTCT AGGTAAGGAC ATGCTTTGGG GTGTCTTTCT GGCCCTTGCC TTTGCGTTTG 300 CGCATAGGGC TCTAGTGGCC CAATTATGTT GTTGCAGTAA AGTTTCTCCT TGCTCTGGTC 360 TGGAGCAGTT GAGGTCATTC ATCCCCTGGA TCTCTGTTGG CACAGGTGGC TTGGCCGAGT 420 GCCACTTTAG GTAACTGTGA CCTGTTTACT CAACTTCTTC CTGGAGTTTT GATATTCTTG 480 TTGTCAGGGC CTTTGAGAAA GTTTATACGA TGGGCTCAGT GAAGAAGCCG CAGCTGTTCT 540 GAAATTAGGC TCCTTTCCCC GTGAATGTGC AGCTATGCGG GTGTGTGGAT CAGGTGCACA 600 GGGCTTTGAG GAATGTGGCG GAGACTCAGT GGCAAGAACA GTTGTCTGTG ATTGCTGGGC 660 CTTGTTTTGA CCCAGTCCCT CACCCCACAT AAGCCTCTCA GCGAGGAACA TGGAAGGGTC 720 AGGCCTCTCA CGTTTCCTCC CCTGTGAGAT TGGATCGCCA CTGTGATGGC ATTTCTCCCC 780 ATCTTCAGTT GCTGGGCAGA CCCTGCGTGT GTGCGCACAT GTCCATGAGC CCACAACCCT 840 TGCATATTTG CAACAAAAGT CTCTGGGGAG AATGAATTTA AATGGACTCT TGACTATTTG 900 TTCTGGAGCG GCACGTGTTT ACTTAAGTCA CCAGCCTCCT TCCTAAATGC AGTCACGAGC 960 TCTCCCAAAC TCCACAGACA CCCAAACAAC CAAATATTCA GAGAGCCCGT GCCCTTGCCC 1020 TGCTTCAGCC CCACAGCCCC GCCTGGGTTG CTGGTCTGAC CCGGCTGGGC AGGGTGGCTG 1080 TGAGCTGCCG GTGTGGCCCC AGGCACCTCA AAGGGTCCTC GGTGTTCAAC AACAGGAAGT 1140 GCTGGCAGGC TTCCCTCGCT AGGGAACTGA AAGTGGTGAC AACAGAGGAT GTGTTCTTCA 1200 GGCTATCAGA TAAAGCCCTC TGCACTGAGA ACTGCTTCTG ACGAGGAACA GAGACTTCAC 1260 TGGTCTCTTC CCCATGCCTT GCCCTTGCCC TAACTAACTT CTGAATTTAT ATCACCTGTG 1320 AGTTCTGCTC TAATTCAGGG ACTTGGGCGG AGAGGTTTCG GACAGTGGCC AAAAGCAAGA 1380 GACTGTCTGC ATGACCCTTT AGAAACACCC GTGACCTGGT GCAGAGCTGA GCCAGCTTTG 1440 GCCACACTGT TTGGGATGCT GACTCAACGC AGCTCATTAT ATCTGATTGA ATTTATCTTT 1500 CATTACTATG CAATCAAATT AAAGGGCAAG AAGGGATTTT TCTCTGTTTT CTGAAAGTGG 1560
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