Tag | Content |
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EnhancerAtlas ID | HS101-09327 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr11:128294130-128296440 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr11:128295857-128295869 | AAACAAACAAAC | - | 6.32 | Foxd3 | MA0041.1 | chr11:128295861-128295873 | AAACAAACAAAC | - | 6.32 | Foxd3 | MA0041.1 | chr11:128295865-128295877 | AAACAAACAAAC | - | 6.32 | GLI2 | MA0734.2 | chr11:128295924-128295939 | TGACCACCCACCCTG | + | 6.11 | Nr5a2 | MA0505.1 | chr11:128295646-128295661 | GAGATCAAGGCCATC | + | 6.05 | ZBTB18 | MA0698.1 | chr11:128294621-128294634 | GAACATCTGGATT | - | 7.22 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_24595 | chr11:128294033-128295631 | Colon_Crypt_2 | SE_24595 | chr11:128295839-128296156 | Colon_Crypt_2 |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I128420 | chr11 | 128290218 | 128296150 |
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Enhancer Sequence | ACATATATAT ATATATGCCG AAGGTCATTC AATGAATTTG TTACCGTCAC TACATAATGG 60 GTTGAGTGCA ACGAAGAATG GCTGAGGCTG CAGCTGAGCT CAGTCTCATT CATGAGAGCC 120 TGAGTCCTGG AGGCCCTGCC AGGAGTTGGG CCCTCCCTGT CTGCCTCCAG GCCTCAGTTT 180 GGAGCGGTCC TCAGGTTTCT GGGTGCTTCA CTTCATTTGT ACTTGGCCGA AGACAGTTTC 240 CTGTTTCTAA GAAAAGACTG CTTGGATGTC TTTTGAGGGC CTTTGGACAG CAAATCCTGC 300 TGGCCTGGGA GGGGCCGAGG GGCAGCACCA GGGGGAAGGG AAGCCACCAG GGAGGGCTTG 360 TTCTCATTAA CCCCTTCCAG CCCGAAGGTG TCCTGGAACT CACAGAGTGA GGCGATTGCA 420 AACGTTTGTC AGATTGGATG AAAAATGAAG ACAAGTTTAT GCTTGGGCCA AATATGCCTG 480 AATTATTTGA AGAACATCTG GATTTGCTTA GCCTAAATGA AAAGATCTTA CATGACAAGG 540 ACTACAGAAA GGGACCTGTG CGTCCAGCAC CTTGGAGCAT CCGGAGAGAC CCTGCCCTTT 600 CTCTGTCTCC CGCTACAGCT CTCTCCAACT CTGCCTTTTC CTTCCAGCTT GGAGTCCCAC 660 AAATGGCTTT TCCAGTGATA TCACACGCTG TTGCCATGGA GGCAGCTGTT ATGGCCAAAC 720 AAAACTGTGT GACCTTCACC CTATGGCTTG CAACCTGTGG CAGAACATGG AAGGGAGTCA 780 CTCTGTGACC ACAGGCCTCA GTGGAGCTCT CTGGGTACAA ATACAAATGG AACTGCTGGG 840 ACACACTGTG GTGGGAACGG AGACCCTGTG ACGGAGCTGG GAAACGCTTG GGAGGGTGGA 900 GCAGCGCAGC CTCCTGCGGC GACAAGGCCA TCCAGACCCT GATGTGAACA GCAGCTGCCT 960 CTCCTCTGCC ACTGCCAGTC CAGCCCCACC CACGCTGGAC TCTGCTCCCC TCTCATCCAG 1020 CTCTCTCCAA GCCTTGGTGA GCCACAATTA ACAGCAATGC TGGCAGTGGC TTACACAAGC 1080 TTTTGATGGG AGAAACGCTA TGCTGAAGGT TATGAAAGCA GGTTCTGGAA CCCTAGCCAC 1140 CTGGGTTCTA ATCTGGGTTC CACGACTCAA CAGCAGTGTG GCTTTACAAA AGCCACTCGG 1200 GATCCCTAAA GCCTCAGTGT CCCAATGTAA GACACGTCAG CCCTTGCAGG GTTATGATCA 1260 TCCATTGAGA TCATGTAGGT GGAATCCTCC TAACAGATCT TTCTGTGTTC ACTCTTGCCA 1320 AAAAATGAAT CTGATCATGT TGCTGCCCCA TTGAAACCCT CCAACAGTTT CCCACCACCA 1380 GGAATAAGAT CCTAACCATG GTCCACAAGC CACACCCGCT GGCGGCCCAT AAAACTCAAC 1440 TCATGGCTGG GCGGGGTGGC TCATGCCTGT AATCCCAGCA CTTTGAAAGG CCAGGGCGGG 1500 CAGATCACAA GGTCAGGAGA TCAAGGCCAT CCTAGCTAAC ATGGTGAAAC TCTGTCTCTA 1560 CTAAAAATAC AAAAAATTAG CCAGGAGTGG TGGCGCACGC CTGTAGTCTC AGCTACTCAG 1620 GAGGCTGAGG CAGGAGAATC GCTTGAACTC AGGAGGCAGA GGTTGCAGTG AACTGAGATC 1680 ACGCCATTGC ACTCCAGCCT GGGCGACAGA GCAAGACTCC GTCTCAAAAA CAAACAAACA 1740 AACAAACAAA AACAAAAACT CAACTCATGC CCTGGTCCAC TGGTGGATCT GCTCTGACCA 1800 CCCACCCTGC CAGGCCCTCT CTCTGCCTTC CAGTGTGCTC TGTGCAGGAG TGTCAGCCTG 1860 CTCTTCTCTT CTCAGGGAGA CCCCCACCCC CTATTGTCAA GTCTTCTGTC TCAGCACAAG 1920 TCACCTCCTC AGCAGGGAAC CATGAATCTA AAGCTGCTGT GTTCCCCACC CCGGGACTCT 1980 CTAGCCCATT TTCTGTGTAG TATTCTTTTT TCCTTTCTTT CTTTTTTATT ATACTTTAAG 2040 TTCTAGGGTA CATGTGCACA ACATGCAGGT TTCTTACATA TGTATACATG TGCCATATTG 2100 GTTTGCTGCA CCCATGAACT CGTCATTTAC ATTAGGTATT TCTCCTAATG CTATCCCTCC 2160 CCCAGCTCAC CACCCCACGA CAGGCCCCAG TGTGTGATGT TCCCCACCCT GTGTCCAAGC 2220 GTTCTCATTG TTGAGTTCCT ACCTGTGAGT GAGAACATGC GGTGTTTGGT TTTCTGTCCT 2280 TGTGATAGTT TGCTGAGATT GATGGTTTCC 2310
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