Tag | Content |
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EnhancerAtlas ID | HS101-10439 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr12:53762180-53763970 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr12:53762832-53762844 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr12:53762836-53762848 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr12:53762840-53762852 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr12:53762844-53762856 | GTTTGTTTGTTT | + | 6.32 | Zfx | MA0146.2 | chr12:53762545-53762559 | GAGGCCGAGGCGGG | - | 6.01 |
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| Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
SE_00711 | chr12:53763583-53767006 | Adipose_Nuclei | SE_26935 | chr12:53762872-53763708 | Esophagus | SE_27963 | chr12:53762947-53768392 | Fetal_Intestine | SE_28934 | chr12:53763053-53768413 | Fetal_Intestine_Large | SE_31931 | chr12:53762875-53763578 | Gastric | SE_34531 | chr12:53762791-53767006 | HCT-116 | SE_34882 | chr12:53762596-53768384 | HeLa | SE_50848 | chr12:53762866-53763590 | Sigmoid_Colon | SE_52902 | chr12:53762879-53763703 | Small_Intestine | SE_53743 | chr12:53762837-53763518 | Spleen |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I053368 | chr12 | 53762586 | 53768254 |
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Enhancer Sequence | GCAGGAGAAT GGCGTGAACC CGGGAGGTGG AGCTTGCAGT GAGCTGAGAT CACGCCACCC 60 CACTCCAGCC TGGGTGACAG AGTGAGACTC CATCTCAAAA AAAGAAAAAG AAAAATTAGC 120 TGAGTGCAGG GGCGAGTGCC TGTAGTCTCA GCTAGTTAGG AGACTGAGGT GTGAGGATCA 180 CTTGAGCCCA GAAGTTGGAG GCTGCAGTGA GCTATGATCA TGCAACTGCA CTCCAGCCTG 240 AGTGACAAAG TGAGATCCTG TCTCAGAAAA AAAAAAAATT GAAAAATTTA ACCATTTGTA 300 CTGTTAAAAA ATCATTTAGG GCTGGCTGGG CGCAGTGGCT CACGCTTGTA ATCCCAGCAC 360 TTTGGGAGGC CGAGGCGGGT GGATCTCGAG GTCAGGAGTG TGAGACCAGC CTGACCAACA 420 TGAAGAAACC CGTCTCTACT AAAAATACAA AATTAGTCAG GTGTGGTGGC ACATGCCTGT 480 AATCCCAGCT ACTCGGGAGG CTGAGGCAGA AGAATCACTT GAACCCGGGA AGCAGAGGAT 540 GCAGTTAACC CAAGGTTGCG CCATTGCACT CCAGCCTGGG CAACAAGAGT GAAACTCCAT 600 CTCAAAAAAA AAAAAAGGTG AGTTTTTTTG GTTTTGTTTT GCTTCGTTTT TTGTTTGTTT 660 GTTTGTTTGT TTGTTTTTGA GACAGAGTCT GGCTCTGTCG CCCAGACTGG AGTGCAGTGG 720 CGCGATCTCG GCTCATTGCA AGCTCCGCCT CCCGGGTTCA GGCCATTATC CTGCCTCAGC 780 CTGCCAAGTA GCTGGGACCA CGCCCGGCTA ATTTTTTTTT GTATTTTTAG TAGAGATGGG 840 GTTTCACCGT GTTAGCCAGG ATGGTCTTGA TCTCCTGACC TCGTGATCTG CCCGCCTTGG 900 CCTCCCAAAG TGCTGGGATT ACAAGTGTGA GCCACCGCAC CCGGCCGGTG AGTTCTTGAC 960 CTGTGGCAGA AGGGCATTCT AGAAGACCAC AACTGTGTGT GTATTAGTGC AATGTCACAG 1020 AGGAAGACAC TTGGCTTTTT TTTTTTTTAA GACGGAGTTT CACTCTGTCG CCAGGCTTGA 1080 GTTCAGTGGC GTGATCTCAG CTCATGCAGC CTACACCTCC TGGGTTCAAG AGATTCCCCT 1140 GCCTCAGCCT CCTGAATAGC TGGGACTACA GGTGTGCACC ACCACACCCG GCTAATGTTT 1200 CGTGTTTTTA GTAGAGACGG GGAAACTCCG TCTAAAAAAA AAATAAATAA ATCATTTAAG 1260 GCCGGGCGCG GTGGCCCACG CCTGTAATCC CAGCACTTTG GGAGGCTGAG GCGGGCAGAT 1320 CATGAGGTCA AGAGATGGAG ACCATCCTGG CCAACATGGT GAAACACCGT CTCTAGCATG 1380 GCAACAGAGG GAGACTCCGT CTCAAAAAAA AATTATAATA ATAATCATTT AGGCCGGGCA 1440 CAGTGGCTCA CGCCTGTAAT CCCAGCACTT TGGGAGCCCG AGGCAGGCGG ATCACGAGGT 1500 CAGGAGATCA AGACCATCCT GGCTAACATG GTGAAACCCC GTCTCTACTA AAAATACAAA 1560 AAAATTAGCC GCGCCTGGTG GCAGGCGCCT GTAGTCCCAG CTACTGGGAG GCTGAGGCAG 1620 GAGAATGGCG TGAATCCGGG AGGCGGAGCT TGCAGTGAGC CGAGATCGCG CCACTGGACT 1680 CCAGCCTGGG CGACAGAGCC AGACTCCATC TCAAAAAAAT AAATAAATAA AATAATAATA 1740 ATAATCATTT AAATCAGAAG AGAAGAAAAT GAACCTAGAA CACCCATCAT 1790
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