Tag | Content |
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EnhancerAtlas ID | HS105-62921 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr4:187543110-187545380 |
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 | chr4:187544189-187544207 | CTTCACTTCCTTCCTTTC | - | 6.08 | GATA2 | MA0036.3 | chr4:187543472-187543483 | TTCTTATCTTT | + | 6.62 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_66818 | chr4:187543986-187545345 | Jurkat |
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| Number: 1 | ID | Chromosome | Start | End |
GH04I186621 | chr4 | 187542639 | 187547206 |
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Enhancer Sequence | GTATACTTTA CAGAATTTTG TCCATAAATG ATGAAAAACA AAAAACAGAA GAAACAGCAC 60 TCTGCTCTTA GCGAAGCCAA AACTCCCTCT CTCGGCTGCA CTGGGAATGT GTGGTGGAAA 120 GACAAGGCTA TCCTTCCACA AAGCAGTTGA GTGAGTCACT TTCCAGGAGT CCCTCAAAAC 180 ACTTCTGGAC CACATTTGTA TTTTCAACGG TTATGACTTA CAAATTCTTA AGATATGTAT 240 TCATTACGAA AGATTTCGAT TCAGTAAGAA ATTGACATCA AGCTTCAAGA GACAATTGTC 300 CATGGATAAA TGTGTGTAAC CCACCCCACT TTACAGGTTT TGAAGATTGC AACAACATTC 360 CCTTCTTATC TTTTTCAGGT CAACTTATCC TCTAGGTCAG TGGTTTTCCC CTGGGGGCAA 420 TTCTGCTCCC TAGGAGACAT CTGGTAATGC CTGCAGACAT TTTTGGTTGT CACTACTTGT 480 CGGAAGAGGG TGCTCCTGGC GTCTCGTGGG TGGAGACCAG GGGTGTTGCT AAGCATCCTA 540 CAACGCACAG GACAGCCCTA CACAACCAAA AATATCTGGT TCCAAATGTC AGCAGTGCTG 600 AAGCTGAGAG GCTGCTCAAA GATAGAGTGT TTTACCTCCT TTTCTTTGGA CCTTTTCAGG 660 CTATACTGTA TGTATCTTTA GCTGCAACCA CAACTCCAGA ATATTGTATA ATTTTGTATC 720 ATCGACTGAA TCTTCAAAGA AACAAGCAGT TCTCTACAGC CCTTTTGGAT AAATCAGGGT 780 GGCGTTGCAG GTTCTCAGGT TTAATCCATC CACGAGCCCA TCCTTTTTCT GTTTCATGAA 840 CAAGCACCCA GAATTCACCA TCCCTGTCAT AGCACAGAAT TTATTTTCCC CAAATGAACT 900 ATTATACTTA CCCAAAACAA AGCTCACTTG CCACTTAACT GCTTTCTCAG ATTCTTGCTC 960 TAGGTTTGCC ACGAGTGTGG CATTTCACAG ACCAGAACTG CTCAGTGTGA GCTGCACACC 1020 AGGGATTCAC CAAGCACTTT GTTCTCCACA TCATTAACAG GAAACACTTC CTCTACAGTC 1080 TTCACTTCCT TCCTTTCATA CATTTTCCAA AAATCCACGG CCATTTTTTA GAGACCAGAT 1140 CCAGCCTGCT TTTCATTAAG TCTTACTGGC TCTGCATCCG AGCCCCAAGG CAGTGCCTCA 1200 GTCTGCAACA GGGTGGAGGC CCAGGGTTTC TCTAGGCCCT GACGCTCTGA GCTGAACCCT 1260 GGCCGAGAAC TGGGTCCTGC TGCCTCTGCC AGGCTTTTGA GACACTAATT TCCGGCCTGT 1320 CTGTACTTAT GAGTCAGTGA TCCCAGGTCC TTCCTGATTG CATTTTTGGC CGTCGTCAGA 1380 ACGCCAAGAT CCTTTTCTCA TCCCACCTGT ACATCACCCT CACTGTCTAA AATTGTGACT 1440 GACTGCCTGG CCTGACACAG GAGACTGGGG CAGCCATGGT GACTCTCTTC ATCCCTGCCC 1500 CTCAGACTTC CCTATGTCTG TACTCACCAG CTGACCTACC ATATTTTATA TTCATTCTTC 1560 TATATCCACT TCTCTCTTAT TGTACAGGAT AATCTTATCT TGCCGATGAA GCTTCAAATA 1620 TGCAAGGCCT CATGTGGAGG AACGAAGAGA CTATCTGCTG TGGAGGAGGC TGGTGCTGCT 1680 AGAACACACT GCTTTCTGCA AAACTTGCTC CCTGCCCTCC AGCCAAGTGG GCATTCTCTT 1740 TGTCCTCAAT CAGGAGAGCA CACTCATCTC AGAGCCCCAG TGTCTGATGC ATCCTCTCCT 1800 GGAAGAGTCT CCTCCCGCTA TTCTTACTGT TTCTGTCTCA TCGCCCTGTG TTTTCTTTAC 1860 AGCATGGATT ACAACCTTGC TCTTTATCGG CCATGCAAGA TTCAGAAACA TCCTCTATTA 1920 TCTGGGGCAT CATGACTCTG GTGAACACAG CTTGGAGCAT GTCACTGATA ACAAGGTTAA 1980 ACAGGAACCC AGCTCGTGAT GGGATACATG AATCCCACAT CCATATAGAT TAAGGCAGAA 2040 ATCATCAGAT TTGCAGGTGG GAAAGCAGCA TCGTGTTTAT GTGAAGAAAC AATGAGGGCT 2100 GCTGAGTGGT AGAAAGTGCC CCTGCCTGGC CTAACAACAG GTTCATTCAC AGACACTGAG 2160 ATGCACTGGT GCTGTTGAAC GACTTCCTAA GGTGGCAGAA AAGGTCTGTA CGAGGCTGGG 2220 GGCTTATTCA CTGACTTTAG CTACAATATG AGTGATTTTT AAACAACTTT 2270
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