Tag | Content |
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EnhancerAtlas ID | HS195-02862 |
Organism | Homo sapiens |
Tissue/cell | VCaP |
Coordinate | chr17:44185250-44186640 |
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 | CTCTATCTCT CTCATAAACA CACTCAATTG GCAAATCTTA TTGGCACTGT CTTCAAATAT 60 ATCCAGTATT CAGCCACTTC TTGCCACTTC ATTGTTAGTA CTTTGGTTGA ATCTTTCTAG 120 ATGAGTCCAA GAGCCTCTAA ATGGGCTTCT AGCTCTCACC CTTGACCACT TTCAGGATAT 180 TATCATGAAC ATAGCAGCCA GCCTAATATT GTATAAAAGG ATAAGTTCGA TCATGTCACT 240 CCTCTACCCA AAACCTAGCC TAGTTGTTTA CCATCTCTAA AAACCCAAGT CCTGACAACG 300 ACCCTGTAAG GCCTCAAACA GAGAGCCTCT ATCACCCAAT CCCTGCTACC TCTCTGGCCT 360 CATCTCCTGT TCTCCTCCTG GCTCATTCCA TTCCAGTCAC TGCTGTTTGC TGAACATGTT 420 AGGCAAGCTG TCACCCACAG GACCTTTTAT TTGCTATTCC TAAAGCAGAT ATCCTCACTT 480 TCTTCAGGTC ATTTCCTTAC ATGACACTTT ATTAAGGCTT TCCCTTAACT GTCCTATAAA 540 ATTGCAACCC CTCTCCAAAT ACCCCCTACA CACCTTTCTT TCCCGCTTCC TGGCTTTATT 600 AATAGAACCT TCATGAAAAT TATTTTTAAT TATCTATCTT TCTTACTGTC TGTTTCCCCC 660 ACTAGAATCA TATCCGGAAA ACAGAGATTT TTGTCTTGTT CACCATAATA TCTCTGGGTG 720 CTTGGAACAA TGCCTAGCAA ATGGCAGGTA CTCAAATATT TGTTCAAAGG GAAGGAAGGA 780 AGCAGGAAGA GAGAGGGAAT GAGGGTAACA GGCTGGAACT ATGATCCTAA CTTTTCCTTA 840 CAAAAGATTA AAACCAAAGT AATTCCAGAC TGAAGCTAAC CCCTTTTCTC ATCTGGTGCC 900 AACAGACCTC ATAAAACTAA CTCTGGCCTC CTCATAAAAC TAACTCTGGC CTCTAATGCT 960 GAAAGCGAGT CAAGCAATTA TAGTCCACAC TCTTAGTCCA AGTATACACA AACCAGGGAA 1020 AATAAAGCTA TATTACAAAG TGAAAACTAC TAACAAGATA TTTGAGAGCT CTTCTTTTTT 1080 TGGAGATAGG ATCTTGCACT GTCACCCGGG CTGAAGGGCA GTGATGCAAT CATAGCTCAC 1140 TATAGCCTCA ATCACCTGAG CTCAAGCAAC CACTCTCACC TCAGTCTCTG CAGTAGCTGG 1200 GACCTCAGAT GTGCACCACC ACGCCCAGCT AATTTTATTT TTTCATAGAA ATGGAGCCTC 1260 ACGATGTTGC CCAGGCTGGT CTCAAACTCC TAGGCTCAGG TGATTCTCCT GCCTCAGCCT 1320 TCCAAAATGT TGGGATTACA GGTGTGAGCC ACTGCACCCA GTCTAATCCC AACCATACAC 1380 AACTTGAATG 1390
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