Tag | Content |
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EnhancerAtlas ID | HS120-01411 |
Organism | Homo sapiens |
Tissue/cell | LNCaP-abl |
Coordinate | chr12:13029740-13031100 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxo1 | MA0480.1 | chr12:13030402-13030413 | TGTAAACAAGA | - | 6.02 |
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| Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
SE_02173 | chr12:13030262-13031253 | Aorta | SE_23547 | chr12:13029794-13031250 | Colon_Crypt_1 | SE_24533 | chr12:13030302-13030703 | Colon_Crypt_2 | SE_24533 | chr12:13030713-13031131 | Colon_Crypt_2 | SE_28138 | chr12:13029843-13031213 | Fetal_Intestine | SE_34394 | chr12:13029943-13032936 | HCT-116 | SE_57272 | chr12:13029850-13031356 | VACO_400 | SE_64427 | chr12:13030014-13031054 | NHEK |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I012876 | chr12 | 13029846 | 13032176 |
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Enhancer Sequence | CCGTCTCTAC TAAAAATACA AAAAATTAGC AGGGCGTGGT GGCGGGTGCC TGTAGTCCCA 60 CCTACTCGGG AGGCTGAGGC AGGAGAATGG CGTGAACCCA GGAGGCGGAG CTTGTGGTGA 120 GCCGAGATCG TGTCACTGCC CTCCAGCCTG GGCGACAAAG CAACGCTCCG TCTCAAAAAA 180 CAAACAAAGA AACAAACAAA ATCTCCTCTG AAAAATGTCA TTATTACCTT TCCTTAGTTC 240 CAGGAGTCCG GGAGCCTCCT TTGTGCAGAG ATCTTTGTAT TGCCACATTA GTGCAATGCC 300 CTGCACATAA TAGATGCTTA ATATATAGCA CTGCACTGAA CTGAAATGAG TAGTGACACT 360 TGCCAGACAG TCTTGCAAAA GAGGAACAGG TGAATCCTTA ACACAATTCA AGGTCTTATA 420 GGAAGAAACT GCCAGTCAAC CAAAACTAAA CCGAGGCATA CATTTCTTTC CTCACCTGGC 480 TTACAATGCT GGAAGGTCTC TGGTTTCCTC TAAAGTGCCC TGGGTTTAGC CCATTAAACC 540 TTATCTGTCT TATAAACCTT GCCATGAATA TGCTTATCAG CTTCTTCCTG GGAGCATAAA 600 ATGGGTTTGG ATAATGACTA TAAAGCGCTG GAATAAGGAA GGTGCTCAAC AGAAGTTGTT 660 AGTGTAAACA AGAGCAGGTT AGAAGTGAGA AGAAGGTGCT CAGAGGACAG AGGAGATATG 720 GGGAAGGACT TGGAATTAGT GGGGTGGAAC TGGGGAGGAG AGCAGGAGGC CTGGCACTGA 780 GAGCATCTCC TTCCCAGCTT GTTCTAGACA AGAGTAGCCT TGCCTGCCAG AAGCCCTGAG 840 ATTACAGGTG AGCTGGATCC CGAGAAATGA AGTCCCTGAC TAATAGCAAA TAAAGACACG 900 GCCATTTGAT AGTTCTGTTC TACATCTCGG AATGGGTAGA AATACAATAA TAGCACCAAA 960 CATGAATTAT GGAAAACAAG CTGTGAATGG AGACATTTGC TAAGAGATGC CAGCCCGGCT 1020 CAGCGAAGTC AATTCATCAG CTATTTTCAC TTGGGAAAGA GAAATTAAGG GCAGAGCCGC 1080 AGTCCCTGCC AAACCTAACA GTCTAAAAAG CAGACTGTGT AACTTACCAA GGCCTCAGGG 1140 CAACATTAGC TGCAAATGAG CTCAGCAGGG CGGGGGCCTC CGCACAGTTC TCTAGGGGGA 1200 GAGATGGCAG GGGCCACAGC CTCTAATGTT AAAGCCACCT GCAGGGCCAG AGGGCCTCTC 1260 TGGAGGCAGA GGGATGCAGC AAAGACTACT TGGCTCTGCA GTCAGGGCTG GGCCGGGTGG 1320 TGCCGCACCG CTTTCTAATG GTAACTTAAC CTCTCCAAGC 1360
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