Tag | Content |
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EnhancerAtlas ID | HS184-13666 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr17:44185380-44186520 |
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) |
EWSR1-FLI1 | MA0149.1 | chr17:44186015-44186033 | AAAGGGAAGGAAGGAAGC | + | 6.04 | EWSR1-FLI1 | MA0149.1 | chr17:44186019-44186037 | GGAAGGAAGGAAGCAGGA | + | 7.55 | ZNF263 | MA0528.1 | chr17:44186028-44186049 | GAAGCAGGAAGAGAGAGGGAA | + | 6.69 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_09447 | chr17:44183178-44188340 | CD14 | SE_18395 | chr17:44183888-44186424 | CD4p_CD25-_Il17-_PMAstim_Th |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I046106 | chr17 | 44184167 | 44186566 |
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Enhancer Sequence | GAGCCTCTAA ATGGGCTTCT AGCTCTCACC CTTGACCACT TTCAGGATAT TATCATGAAC 60 ATAGCAGCCA GCCTAATATT GTATAAAAGG ATAAGTTCGA TCATGTCACT CCTCTACCCA 120 AAACCTAGCC TAGTTGTTTA CCATCTCTAA AAACCCAAGT CCTGACAACG ACCCTGTAAG 180 GCCTCAAACA GAGAGCCTCT ATCACCCAAT CCCTGCTACC TCTCTGGCCT CATCTCCTGT 240 TCTCCTCCTG GCTCATTCCA TTCCAGTCAC TGCTGTTTGC TGAACATGTT AGGCAAGCTG 300 TCACCCACAG GACCTTTTAT TTGCTATTCC TAAAGCAGAT ATCCTCACTT TCTTCAGGTC 360 ATTTCCTTAC ATGACACTTT ATTAAGGCTT TCCCTTAACT GTCCTATAAA ATTGCAACCC 420 CTCTCCAAAT ACCCCCTACA CACCTTTCTT TCCCGCTTCC TGGCTTTATT AATAGAACCT 480 TCATGAAAAT TATTTTTAAT TATCTATCTT TCTTACTGTC TGTTTCCCCC ACTAGAATCA 540 TATCCGGAAA ACAGAGATTT TTGTCTTGTT CACCATAATA TCTCTGGGTG CTTGGAACAA 600 TGCCTAGCAA ATGGCAGGTA CTCAAATATT TGTTCAAAGG GAAGGAAGGA AGCAGGAAGA 660 GAGAGGGAAT GAGGGTAACA GGCTGGAACT ATGATCCTAA CTTTTCCTTA CAAAAGATTA 720 AAACCAAAGT AATTCCAGAC TGAAGCTAAC CCCTTTTCTC ATCTGGTGCC AACAGACCTC 780 ATAAAACTAA CTCTGGCCTC CTCATAAAAC TAACTCTGGC CTCTAATGCT GAAAGCGAGT 840 CAAGCAATTA TAGTCCACAC TCTTAGTCCA AGTATACACA AACCAGGGAA AATAAAGCTA 900 TATTACAAAG TGAAAACTAC TAACAAGATA TTTGAGAGCT CTTCTTTTTT TGGAGATAGG 960 ATCTTGCACT GTCACCCGGG CTGAAGGGCA GTGATGCAAT CATAGCTCAC TATAGCCTCA 1020 ATCACCTGAG CTCAAGCAAC CACTCTCACC TCAGTCTCTG CAGTAGCTGG GACCTCAGAT 1080 GTGCACCACC ACGCCCAGCT AATTTTATTT TTTCATAGAA ATGGAGCCTC ACGATGTTGC 1140
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