Tag | Content |
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EnhancerAtlas ID | HS184-13732 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr17:47448240-47449240 |
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) |
Lhx3 | MA0135.1 | chr17:47448603-47448616 | GAATTAATTAATT | + | 6.29 | Lhx3 | MA0135.1 | chr17:47448604-47448617 | AATTAATTAATTA | - | 6.78 | POU6F1 | MA0628.1 | chr17:47448605-47448615 | ATTAATTAAT | + | 6.02 | POU6F1 | MA0628.1 | chr17:47448605-47448615 | ATTAATTAAT | - | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_11408 | chr17:47447492-47452144 | CD20 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH17I049370 | chr17 | 47448304 | 47449608 |
|
Enhancer Sequence | AGAAGTGAGG CCACCACCCA CCTGCAATAG CTTGGCTTCC TGGATCCCTA AGCAAAGGTA 60 GAAAGGAACC CTGGGGTTAG GTAGTGTGGG CAAAGACCTG CAGCCGGAGA ATTCCCTATC 120 CTCCTATCTC AGAGCAGACT GTTGCAGCCC TCAATTCATC CTTTGGGGGT TCTGCCTCAG 180 GCTCTTGTCT CCAGTAGAAT GATCTAAGGA TCTAAGGGAG CGAGGCCCAA ATTGTGTTTG 240 AGTCTTTAAA GAGACTCACA AATCTTTTTA AGCAGCAAGC TTAATTGTTG TCTGTAATTG 300 ATGTGACATA TGCCCCAGAG GCATGCACTG AGGTCCAATT GAGATGGTTT TTTAAAAAAA 360 TTGGAATTAA TTAATTAAAG AAGGCAGCTG CACGGGCCTG GTAGTTGGTG CCAAGCTCTG 420 TAACCCTAAA CCAGCCAACC AACCCAACTG GCCTCACCAC CTGAGGAACA ATCCCTGCAG 480 CTCTCATGGA GATGAGATGG GATGGAAGTG CTGGGAAGCA GTGCAGGGAA GAGGGGCTTG 540 CAAGGGGGAA CGGTGGGGCT CAAGGGACCC ACTCTTCACT TTCATGATCC CCCAAAGGCT 600 TAGCTCTTGA GAACTGTTCG GGGGGACTAG GTAACTGGGA AAAAGGGGTG GGAAATTCAA 660 ATGGAAGTAT GTGAGGGGCA GGCGAGATTT TGGGGGAGGG GAAGCCAGGG GGCTGGAATG 720 GGAGGGGGAG GGGTTCGCAG GTGTGAGAAC GGTGTAGCAG CTCCGGTAGG GAATGGAAGG 780 ATCCGGGGGT GGAGAGGCCT ATGGGCGGAG CTCAGAGGAG GTGGAGCCTG GGTGTGGGGG 840 CGGTAACATG GTGCCTGAGG CCTCAGCACT CAGAGGAGGT GTTAATTAAA CCCCTTACCT 900 GAGGTCGTTA ACAATGCTGT GGCAGCTTTT CCTAGGAGTT GGGTTAATAA CAGTAATAAT 960 AACAATTAAC GATAATGAGA CCTTATCTGG AGAAAGTTGT 1000
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