Tag | Content |
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EnhancerAtlas ID | HS041-13920 |
Organism | Homo sapiens |
Tissue/cell | EWS502 |
Coordinate | chr22:21973590-21975800 |
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) |
Gata4 | MA0482.1 | chr22:21974500-21974511 | AGGAGATAAGA | - | 6.14 | NR2C2 | MA0504.1 | chr22:21974809-21974824 | CAGGGTCAGGGGGCA | + | 6.02 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_41896 | chr22:21973533-21974030 | LNCaP | SE_41896 | chr22:21975076-21975674 | LNCaP |
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| Number: 2 | ID | Chromosome | Start | End |
GH22I021619 | chr22 | 21973534 | 21974030 | GH22I021620 | chr22 | 21975077 | 21975674 |
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Enhancer Sequence | CTTGTACAGG GAGGTGATAC CACCTACCCC TGAAGAGGCT TAGAGACTGA ATTAGAGGCC 60 ACCCTGGCCT GCAGAGAGCT TTCCAGGCCC CTTGCCCCTG CTTGCTGTTC ACAGTCCACC 120 CTCCTTGCCC ATCCACCCCC AACAAACGTG GAACCTGTCA GCATTGCATG CGCAATGCCC 180 TCCTCGCCTC TGCCCCACTG CTTCACCTCT ACCCACTGTG GTCACAGGAG CCCTCTCTTT 240 CCCATTCTCA CCAGGCACAG TAAAAAGCAG AGGTTAGGCA GGTGGGTTTT GGACACCAGG 300 CCAGGAGTAC TTTGTGCTGT GGCCCTCACT TAATGTGTGC TGTTGAATGA TTATGCCTTT 360 GCATATGACT CAGCCAGCAT CAGCATTTTG TTTTATTTAT TTACTTTTGA GACAGAGTCT 420 CGCTCTGTTG CCCAAGCTAG AGTGCAGTGG CACGATCTCG GCTCACTGCA ACTGCCGTCT 480 CCCGGGTTCA AGCGATTCTC CTGCCTCAGC CTCCTGAGTA GCTGGGACTC TAGGCATGGG 540 CCACCATGCC TGGCTAATTT TTGTATTTTT AGTAGAGACG GGGTTTCACC ATGTTGCCCA 600 GGCTGGTCTT GAGCTCCTGA CCTCAGGTGA TCTGCCTGGC TAGCATTTGC ATTTTAATCC 660 ATTTCTTGTA ATGCTGAATG AACAATATGA GCCCTTAATA AAGGAATTGA CCAGGTGCAG 720 TGGCTTCATG CCTGTCATCC TAGCACTTTT GGGAGGATGA GGCGGTAGGA TCACTCAAGC 780 CCAGGAGTTT GAGACCAGCC TGGGCAACAT AGTGAGACCC CATCTCTACA AAAAACTAGG 840 CCAGGAGCAG TGGCTAACAC CCGTAATCCC AACTACTCTC AAGGCCAAGG TGGGAGGATT 900 GTTTGAGCCC AGGAGATAAG ACTGCAGTGA GCTGTGATTG CACCACTGTA CTCTAGCCTA 960 GGTTAAAAAA AAAAATTAGC TGGACGTGAT GGCATGTGCT TGTAGTCTCA GCTACTCAGG 1020 AAGCTGAGGC AGGAGGATCA TTTACACCCA GGAGTTTGAG GGTACCGTGC AGTAAAGTAT 1080 GATTGAGCCA CTGCACTCCA GTCTGAGTGA CAGCAAGACT GTCTAAAAAA AATAAGAAGG 1140 AATTTGTGGC ATCAGCAGTT CGGAGAAGAG GGGCACTGTT TTACAGTGGG AAGGAACATT 1200 CTGAGGGTGC TGGTCCTGAC AGGGTCAGGG GGCAACTGTG GCAAAGTATG TGAGGAGGTG 1260 TGGGTAGCAG CTGCTTCTGA TTCCCCACTA TCCTTCCACC CTGGGGCACG TCTGGGCTAC 1320 GGCACCTAGG GGGAGTACTG TGGCACCCAT CAGAGCCATC AGCGTGACAT CTGCCTGTGG 1380 TCTTGACAAT GTGATGCGAT GGCGGTTGTC AGCTTCCCAT TGGCTGGCCC CAGTGACCCT 1440 TTCTAGAGGG TTCAGAAACT CCTAAGGGTC TTCCAGAGTT GGGTCATTGC GCATTGACAA 1500 GTGCAGCGCC ATCACATACC CTTCTCTCTA GTGCCCACTC AGTCACCTTA ACCGAAACTT 1560 CCCTGAGCCG AGCATGGTGC TGGGTGCTGG GCTGATGCAG GGAAGTTCTA CCCGGTCCTG 1620 CCCTGAAGAA AGTGACCCTG TGTGCATGCA TGAGAGTGAG CAGTCAGTTC AATACTAGGC 1680 CTCCTATCTC CAGAGTACAC AAGAGGACTG GATTAGCCGG GCATGGTGGT GCACGACTGT 1740 AGTCCTGGCT ACTTGGGGGA CTGAGGCTGG AGGATTGCTT GAGGTCAACC CAGGAGGTTG 1800 AGGCTGCAGT GAGCCAAGAT GGTGCCACTG CACTGCAGCC TAGGTGACAG AGTGAGACCC 1860 TGTCCCTCCT CCCCAACCCC CCGCCAAGAA AAAAGGGCTG GGAGTGACTG AGGGCTAAGA 1920 CCTCCCCAGG TGTTAGGTCA GGAAGGCTTC CTGGAGGCGG AAGCACATCA CTGTGAACAA 1980 TTATCCACTG TAGTGTTAGC TATTTGTTGT CCATCAGTGT CTTCTAATCA CAGAGGAAAG 2040 ATGAGTTTTC TGGCAGTCAG AATTTTGGAT AAATAGGAGG CAGCTTTGGC TTAAAAGCAC 2100 ATTAGCTGTA AATCAGTTGT AAAGCCAGAG TTTTGTTCCC GGATTAGCTG CCTCTTGCCT 2160 GTGCCATTTC TGAGACTGTG TTAACCCCCC ATGCCTTGTC CTTCTCTTGG 2210
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