Tag | Content |
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EnhancerAtlas ID | HS129-18027 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr19:18879600-18882250 |
Target genes | Number: 19 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GLI2 | MA0734.2 | chr19:18880408-18880423 | GGACCACCCACGGCC | + | 6.4 | RREB1 | MA0073.1 | chr19:18881377-18881397 | TGTGTGTGTGTGGGTTGTGG | - | 6.94 | TP53 | MA0106.3 | chr19:18881796-18881814 | TGCATGCATGGGCATGTA | - | 6.05 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_28464 | chr19:18879217-18880952 | Fetal_Intestine |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I018767 | chr19 | 18878793 | 18880672 |
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Enhancer Sequence | TCGGTAAGCC CAGGGTGGGG TCCCTCGGGG CCTGACTGGG GGTCTTGTAG AGGACAGCCC 60 GGGGGCTGCA GAACAGTCGG GTTACCTGCT GCATGGGCCA GGGGTCAGAA CCCCAGCGAA 120 CGCTGCCTGG GCCCACCTCT CCACGGGGCT ACCCCTTGGA ATCAAACTGA GACTGTCACT 180 CCCTGTAGAG ATGGAGAAAC TGAGGCACGA GCAGGTGGCT GGCCCCAGAT TCCACCCAAG 240 GTGGGCCACC CCATGTTTAA CTGCCGAGCA CCCCTTCTTG GCCTCTCTGG CCCCTCCCAC 300 CTGAAGCCAG GCTTCCTAGG AGGCAAGAAG AGTACGGCGT TCTCAGGGCC AGGGCGCAGG 360 CCGGGGGCCG GGGATGACGT GAGCTTATCA GAGAAGGAAA GACGAGGCCA GTCCAAGAGG 420 CGGCAGCCCG TTGGGCACAG CGCCTGGGGC CCAGGGCTGG GGGCTGCAGC TCAGACCATT 480 GGACTTTTCT GCCTAGGGCC GGCTCAGGCA GACAAAGGCT GGGCTTTAAC CCTGTACCCA 540 CAAACCTTCC TGACTGTCCA GACCACCTGC TTGCTCCAGC GGCGCGGGCT GGGTGGCAAA 600 CAGCTGCATT GGGCCACATC CAGGGAAACA GGGACTTGTG TTCCGGGCAC AATGAGTCCT 660 CCCACTTGAC CCCGACTGCC AGCCCCAGGC TAAATGTCCT CCAAACATTG TGTGCTCTGC 720 AAAGAACAGC CGCCTGAGCT GGGTGGGGCA GGCAGGTGAG CCTGTGGGTA GACACCCATG 780 TTCCCAAGCT GCTCTGACCT CACGGAGGGG ACCACCCACG GCCCCTGGGT GGAAGAGTGC 840 CCAAGTCCTT TCTTTGGTGG AAACACAGCA GGTCCTGGGG GAGGCTCCCA AGGTGGGGCC 900 TCGCCTTGGA GCTGGGTGGT TCTTGGAGTC ACAGGGTGTC TGGGCCAGGT GCAGGGACGG 960 CCCTTCTAGG GCTCTTGGGT CAGGCTGTCC ATGTCCAGCA CCCTCACACA ACAAAGACGG 1020 CTTCCTGCCC CCACTTCAAG GACTTCTAGC CTCCTGGGGT TGAGGGGGGA CTCTTGAGTT 1080 TTTGCACAGA CTCACCCAAA TGAGAATCTC CCTCTGATCC CTTTGTCCTT TCCAACTCCA 1140 GGAAGGCCCA AGTCAGCCAT CCCTAAGTAA CAGTGCTGGC ACCTCCATCA CCCACGCAGG 1200 CGAGCTCACC GCCACCCCCC GCCCTACCCC ACCCCGCCCC ACCTGGACTC AAGCCCTACC 1260 CCAAACTGCC CAGAAGGCGC CACCAAGGAC ATGGGGGAGA CAGCAATTAT AGGCCCTGGA 1320 CCGGTCAGGC TGGGCCTCAT TCAGTGACTG GCTCAGACAG GTCAGGCAAG TTGTCTGCAG 1380 GCACACAGCA TGGCTGGGCC GTGCTAGGAC AAGAGAGTGG TCTGAATCCG GGGCCTGGCC 1440 TGGCCCGACC TGCCTCTGAA AGTTCTGGGT CATAGCAGTG AGATGCCCGG GCCTTTCGTC 1500 CCTCGAGCAG GTGGAGGAAG TGACTGCCCC TTGCAGGTCT CAGATGGCAT AACCCAGGCA 1560 GGTTTGTCCT GCAGCAGGGC AGGGATAGTG ACTGCGCCAT GCTGGGAGCC TGGGCTACCA 1620 GCAAGATGGC CTTCACTCAG TCCCCACCCC CAGAGGTGGG CCAGACCTGC TGGGCTGCAG 1680 ACTTAGGGGC TTAGAGAGCC AGGGGACCTG CCCAGGGCAC ACAGTCAGCG AGAGCCGGGA 1740 ACAGGAGGCA GCCTTGGGTT TTCCCTGCCC ATGGCGGTGT GTGTGTGTGG GTTGTGGGTG 1800 TGCACAAGTG GGTGGGTGCG GGTGTATGTG GTGTGCACCT GCATGGGTGT GCATGCATGT 1860 GAATGTGTGT GCATGTGTGC ATGCGTGGGT ATGTACATTT GTGGATGTGT GGACATTTGT 1920 GGATATGTGG ACATTTGTGT GTGGATATGT GTGCTTGTGT GGGTGTGTGC ACACGGTGTG 1980 TACATTTTGG TGTGTGAATA TATGTGTGTG TGGGTGTGTA CATGCGTGGG TGTGTCCATG 2040 TGGGTGTGGG TGTGCATGTG GGTGTGGGTG TGCATGCGTG GGTGTGTACA TTTGTGTGCA 2100 TGTGTGCATT TGTGGGTATG TACGTTTGTG TGTGGATGTG TGCCTGTGTG TGTGCATTTG 2160 TGGGTGTGAG TATGCGTGTG TGTGCATGTG TGGGTGTGCA TGCATGGGCA TGTACATTCA 2220 TGTGTGGATA TGTGCACATG TGTGGGTGTG CATGTGTGGG TATGTATATT CTAGTGTGGA 2280 TATGTGTACA CGTGGGTATG TCTGTGTGGG TGTGCATGCA TGAGAGTGCA CACGTTGCTA 2340 TATGGCTCTG AGCCTGCTGA GTCAGGGCCA ACCCTCTGAT CACCCTCCTG TAGCTCCAAG 2400 AAGGAGGGCA GTTATTCACC CTCCACGCCG TTCCTTCCTG GGTTCGGGGG CAGCTCCCCG 2460 GAGGCTCAGG TACCCACCTT TCCTGCAGGT GTCCAGGCTC CTCTGCCTAC CAGTGGGGTG 2520 GCGACCATCA CCAAGGTGTG AGGGGCGGGG GGACCTGCCT GGGGGCTGAT CAGGCTGCTC 2580 CCGGGAAGCA GGGACTGGAG CCCGGGCTTG GGCAGCTGGG CTGCGGCGTG CTGATCTGTC 2640 TGTCATCGCA 2650
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