Tag | Content |
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EnhancerAtlas ID | HS184-14787 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr18:55415180-55416470 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL2 | MA0478.1 | chr18:55416150-55416161 | GGATGACTCAT | + | 6.62 | JUN(var.2) | MA0489.1 | chr18:55416147-55416161 | TAGGGATGACTCAT | + | 6.17 | JUNB | MA0490.1 | chr18:55416150-55416161 | GGATGACTCAT | + | 6.62 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_23224 | chr18:55415170-55415980 | Colon_Crypt_1 | SE_25111 | chr18:55414943-55416007 | Colon_Crypt_3 | SE_29272 | chr18:55414862-55417287 | Fetal_Intestine_Large | SE_45764 | chr18:55414670-55417359 | Osteoblasts | SE_50343 | chr18:55415096-55415971 | Sigmoid_Colon |
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| Number: 1 | ID | Chromosome | Start | End |
GH18I057747 | chr18 | 55414836 | 55417490 |
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Enhancer Sequence | GGAAATACTT GCATTTGGCT TGAAATATCT ACAGAGCTTC CTACCAACAG TCAGCAATTC 60 TATCTGTTCT GGCTTTCAGA GTTTGAACAG GTCAAATATA AGGAGTGTGT CCAAGCTTCT 120 CCTACAAATC TGATCAGTTT AAGCACCCAT GGTAAGACTT CTGATGTAAG GCTTCTGAAA 180 CTCCCCATGT TTTCCTAGGA TGATGGTGGC GTGCGTTTAC AGAGAGCTAA CTATGTGTTC 240 TATGCATCAG GCTCTCCACT ATGTATTCGC ATTAGCTTAC TTTGTTTGAG GATCAAATTA 300 TTATCCCCAT TCTACAAATA AAGAAACTGT AACTGAGAGG TTAAGTTCTT TGCCCAAGGA 360 CATATAAGGG GTAACCAGAA TAAAATCCCT TGGAGACATG CTGCCACAAG CCAAGGAACT 420 TCCAGAAACT AGGAGAGAAT CCTGAAACAG ATCCTTCCCC AGCACCCTCA CAGGGAAGAT 480 GGCCGTGCAA AACCTTGATC TTGAACTTCT GGCTTCCAGA TTTGTGAGAC AATAAGCTTC 540 TGTTCTTTAA GCTGCTCTGT GTGTGGTACC TTGTTACAGC AGCCCCAGCT AACTAATATA 600 TGGCTTGAAT GTGTAGCTTT AACATCGGAG AGGGCCTTTC AAATTCCTTA ATTCCAACAA 660 ACAGAGGACT CCACAGTCAG GTACTGCAAA TTTGTTACTT AATGTCTTTA AATTCTGAAT 720 CCACCTTTGC CAAGACTATG TGCACAAAAG GAAAAACTGT GGTTACCTTT TGTAACAAGT 780 TATATAAATA AGAACTAAAT GACCATGTTT TCTTTTCTCT CTTCTAATTA CCCAAAGGTT 840 AACATGCTAT TTTAAAGTTT AATTTAATTT AATTTTGCAG CTTACCCAGG TTTAACAGTT 900 ATTTGCAGAG AATAATCAGA AGGAACTGCA ACTGGTGTTT AATGCAAATA AGGCCAGGCT 960 GCTGAACTAG GGATGACTCA TGCAGGCCTT GTGCAAACAT CTAGTCTGAT TTGCATTTAA 1020 GAGAAAAGGT ACACCTATAG AAGTATCCAA CATGTATTAA AACATCTTCA AAATGTTTTG 1080 GAGTTTTAAA GAAGTGCCCA TTAAAGATGC TTTCTGCTCC ACCTCTTAAA AAAAGCATGG 1140 CCCCAGGAAA AATGATAATG TATTCTAGAA CTTTTTTCTG CTGTGATATT TTCTCCTCCC 1200 AATCAATGTT TGCTTCCCCT TTAAAATCTC TGTGTACTTT CATGGGTGCA GTAGCACATG 1260 GTGATGAGGG CTTGGGTTTG ATTGAGCAAT 1290
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