Tag | Content |
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EnhancerAtlas ID | HS161-02359 |
Organism | Homo sapiens |
Tissue/cell | PC3 |
Coordinate | chr11:413380-414820 |
Target genes | Number: 45 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr11:414397-414418 | CTCCTCTGCCCCTCCTCCCCT | - | 6.34 | ZNF263 | MA0528.1 | chr11:413878-413899 | CCCTCTCCCCTCCCCACCTTC | - | 6.54 | ZNF263 | MA0528.1 | chr11:414394-414415 | CCTCTCCTCTGCCCCTCCTCC | - | 6.89 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_23605 | chr11:414318-418165 | Colon_Crypt_1 | SE_23968 | chr11:414308-415071 | Colon_Crypt_2 | SE_24885 | chr11:413237-413970 | Colon_Crypt_3 | SE_24885 | chr11:414416-418679 | Colon_Crypt_3 | SE_27233 | chr11:414457-418242 | Esophagus |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I000413 | chr11 | 413238 | 413970 |
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Enhancer Sequence | CCCAGGGGAA CCACCCACTG AGGGTCCTTA AAGCACACAC TTCCCAGGAA ACCAACCCCT 60 CACAGCAAGC CCGGGAGGTC ACACCGCCAG CCCAGCAGAA CCCCTGGCAT CTCCTGCAGT 120 GCTTCCGTGA CCGCCCCAAG CTCAGACCTC AAAGTCCTCC CTCCAAAAGC AGCCTCAGAG 180 CCTTCTGGAA GTCAAGGGCA GACTGCCAGG ATACGAGCAC AGCAAGAAAG CAGGTGCCCT 240 CCCCTGCAAA CCCTCCTCTG CACCCTCTCC GCTGCCTGCC TCTCCTTGCA CCCTCTCCCC 300 TGCACCCTCT CCCTGCAAAC CCTCCCCTGC ACCCTCTTCC CGCACCCTCT CCCCTGCTCC 360 CTCTCCCCTA CGCACCTTCC CCTGCACCCT CTCCTCTGCC TGCCTCCCCC TGCACGCTCT 420 CCACTCCCCA CCTTCCCCTG CCCACCTTCC CCTGCACCCT CTCCCCTGAA CCCTCTCCTC 480 TGCCTGCCTC CCCCTGCACC CTCTCCCCTC CCCACCTTCC CCTGCACCCT CTCTTCTGCC 540 TGCCTCCTCC TGCACCTTCT CTCCTCCCTA CCTTTCCCTG TACTCTCGTC TGCCTACCTT 600 CCCCTGCACC CTCTCCCCTC CCCACCTTTC CCTGCACCCT CTCCCCTGCA CACCTTCCCC 660 TGCACTCTCT CCTCTGCCTA CCTTCCCCTG CACCCTCTCC CTCCCCACCT TTCCCTGCAC 720 ACCTTCCCCT GCACCCTCTC CTCTGCCTAC CTTCCCCTGC ACCCTCTCCC CTCCCCACCT 780 TTCCCTGCAC CCTCTCCCCT GCACACCTTC CCCTGCACCC TCTCCTCTGC CTACCTTCCC 840 CTGCACCCTC TCCCCTCCCC ACCTTTCCCT GCACACCTTC CCCTGCACCC TCTCCCCTGC 900 ACCCTCTCCT CTGCCTACCT TCCCCTGCAC CCTCTCCCCT CCCCACCTTT CCCTGCACCC 960 TCTCCCCTGC ACACCTTTCC TTGTACCCCC TCCCCTCCCT AACTTCCCCT GCACCCTCTC 1020 CTCTGCCCCT CCTCCCCTGC ACACATCACA TACACACAGC CCTCTGGCCC ATGTGCACCT 1080 GCACAGAGCT TCAGTCTCAG CCCGTGTGCA CACTTGCACC TCCTACACAG CACACTTCCT 1140 ACCACACACA CCTCCCATTA CCACTGCACA CAGCTTAGGC TGCAGACCCC TCACACAACT 1200 GTTGAGTATA TACAACACCC ATTGCAACGC TTGTCACAGA GCCTAGGACC ACAGGCACCC 1260 CACAGCACAC ACACTGCACC TGACACCCAC CCTTGGCCGC TGATGCGACA CAGCCTCCTG 1320 CTGCCCCTCG CTCTGTCTCA CACACACATG CACACACATG CATATGGGTC TTGGGCGCCG 1380 TGGGCCTCCT CTCAGCCAGG CCCTGACACA GGCTCACTCA GAGCAGCGGG GAAGGCAGTC 1440
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