Tag | Content |
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EnhancerAtlas ID | HS003-03800 |
Organism | Homo sapiens |
Tissue/cell | A549 |
Coordinate | chr1:222059970-222061280 |
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) |
BCL6 | MA0463.2 | chr1:222061242-222061258 | CATTCCTCAAAAGCAC | - | 6.35 | FOSL2 | MA0478.1 | chr1:222060687-222060698 | GGATGACTCAG | + | 6.32 | JUNB | MA0490.1 | chr1:222060687-222060698 | GGATGACTCAG | + | 6.14 | RREB1 | MA0073.1 | chr1:222060325-222060345 | GGGAAGGGGTGGGTTGGGGG | - | 6.22 | RREB1 | MA0073.1 | chr1:222060324-222060344 | TGGGAAGGGGTGGGTTGGGG | - | 7.16 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_36705 | chr1:222058928-222062088 | HMEC | SE_55946 | chr1:222059265-222061847 | u87 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I221886 | chr1 | 222059486 | 222061718 |
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Enhancer Sequence | GTGACATGGA AGATCAAGTT GAAGGAATAT TCTAAAGCCT ACGACAAATA TCCATATCTC 60 ACCATTGTTA GTACAAGGGG CCTGAAATAA AATTCCCTTG GGGTAAGATT GCACACAGGA 120 GGCTACATCT GCTGTGCAGC TCCCCAAAAC TTTAGCCACT CTGACTCATC CCAAGGGGAA 180 GAATTTTGGC CACCTGAGTT CCTGACTTGG ATTCTGACTG TGGCTTTTAG CCTTTGCATC 240 ATCCTGCATC TTAAGGATTG CTCTGTCTGT CTCTCCTTCT CTGTCCTGGG TGAGCAAGCT 300 GCTGGCATCT CCTGTCGGCC ACAGGAGGTG TGTTGACAAG GGCCAGGAAA TATGTGGGAA 360 GGGGTGGGTT GGGGGGAGTT TCCTAGGCAG CGTTCCTCTA GGAACTTTCT TCTCTAGGAA 420 TTCTCTTAGA TCAGCATCCA TTGCCTGTCC ACTGGGTCAT AAGCTTTCCT TATGCACGTT 480 CAGTTGTTAA ATCTACAACA CCTCTCGCCC CCACACAGAC TTTCACTCCC GCTCAAGAGA 540 GGGGTCAGGG TGTGTGTGTG TGTTGTGAGC AAACTCCTTC ATTGCCATGG ACCTGGCAGA 600 GGCACAAGCC AGCCCCATTC CAGGACCATG TGACACTGGC TGGGTTACTC ACTTGTTTGC 660 CCTCCAGCAG GGGCAGCCGG GGACACCTCC CTAGAGTGAC TACAGCGTTT ATCCCTGGGA 720 TGACTCAGCC CAAGCCTCCC TCTGCCCAAA AAGGGAATCT GAGGCTGGGG CTGGAGATGG 780 GGCCTGTTGA TTAGCCGCAT CTATGGTTGG GAGAGCATAG AAACTACCTC TCACCTGGGA 840 AACATGAGGG ACAGAGTGAG TAATGCTCAG ATCAGTGGCT CAGGAACTCA GCGTGAAACA 900 TAAGTTTATT TGAGAAGCTC AAGTGACAGG TGGAGCTTTG CTTCCAGAAC CCCAAGGAAG 960 ATCCTACTCA GCCACCTAAT GATAACATTT TCATTTCAGA TTTCCATTCA TTTCATCTCA 1020 CTGACTTCAC TCTCACCTTT ATTTTGTTTT CGTCATTTCT GGAGTGGGTC AATTACTTAA 1080 CCCTGAATAG AGATGTGATA TAGCAGAGTC TTAGGGTGGG TTCTGGCTGA TTCCTCATCA 1140 AGAATAAGAT TCTATTTCCT TTGTCCTGAA CAGGATAATC TCTTCAGATT ACAAAGCTGT 1200 ACCTACCTAG TATTGTTTGT TGATGTTTCT GTTGTTTATA AACACTGGTC TCATCTCTCC 1260 AAGAGCATAA TACATTCCTC AAAAGCACTC GCTTCCCTTA TAGTTCTAAT 1310
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