Tag | Content |
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EnhancerAtlas ID | HS069-00017 |
Organism | Homo sapiens |
Tissue/cell | GM18951 |
Coordinate | chr1:2342670-2343820 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Zfx | MA0146.2 | chr1:2342915-2342929 | CCCGCCTCGGCCTC | + | 6.01 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_24340 | chr1:2343111-2346064 | Colon_Crypt_2 | SE_25169 | chr1:2343208-2346524 | Colon_Crypt_3 | SE_27514 | chr1:2343120-2346479 | Esophagus | SE_41711 | chr1:2342986-2346400 | LNCaP |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I002408 | chr1 | 2339732 | 2342704 |
|
Enhancer Sequence | TTTTTTTTTT TTTTTTTTTT TTGAGATGGA GTCTCACTCT GTTGCCCAGA CTGGAGTGCA 60 GTGGCACGAT CTTGGCTTAC TGCAACCTCC GCCTCCCGGG TTCAAGTGAT TCTGTCTCAG 120 CCTCCCAAGT AGCTGGGATT ACACGCACGC GCCACCACGC CCTGCTGATT TTTGTATTTT 180 TAGTAGAGAC GGGGTTTCAC CATGTTGTGT AGACTGGTCT CGAACTCCTG ACCTCAAGTG 240 ATCCACCCGC CTCGGCCTCC CAAAGTGCTG GGATTACAGG CGTGAGCCAC CACACCCGGC 300 ATCTTTTTTT TTTCGTTTTT TAATCGGTGA TGGGGTCTGG CCCCGTCGCC CAGGCTGGAG 360 TGCAGCGGCA CAATCATGGC TCACTGCAGC CTCATCCCTC GGGCTCAGGC GATTCTCTTG 420 CCTCAGCCTC CTGAAGAGCT GGGATTACAG ACGCCGCCAC CACGTCCGGC TAATTTTCAG 480 ATTTTTTGTA GAGACGGGGT CTTGCCATGT TGCCCAGGCT GGTTTCAAAC TCCTGGGCTC 540 AAGCGATCCT CCCGCCTCTG CCTCCCAAAC TGCTGGGATG ACAGGTGCTG CTTCATTGAG 600 TACACTGGCT TCTGTACTCA GCTCCCGGCC TGGTGAGGCA GGCAGGGCCT GGCTGAGCCT 660 ACACTGGGGT CAGCAGGGCG AGGGGCCTGG GCTGCTGCTC AGGCCTAGGA AAGGCCGGGG 720 TCAGTGTGAA CCGGACCGAG GTATGAGGCG TTCGCGCCGC GGGCGCTCTG ACCCCTCTGC 780 TCACAGGGGA GGATCGGAGG GAGGCTTGAA GCACTTGCCA AGGCCTCACA CCTGGAGGGG 840 ACAGAGTCTT CCCCAGCCGC TGGCGTCAGC TGGACCTGCC CTGAGCTGGG GACGGGAAGG 900 GCTTGGGCGG GAACTGGAGG CCCACGCAGG TCCCCCGCGG TGTCTGCGGC CTGTGCCTCT 960 GGGGCCACCT GGCCAGGGAG GGCAGGAGGT GCCCCGCACA TCCCTGAATG GCCGCAGGGC 1020 AGGCGAAGGA GACTGCCGGG TCCCAGGTTG TGGGACGGGC CCAGGCGACC GTGACCACAC 1080 ACGGCAGACA CCCCGCCTCC ATGAGGGGCA ACACCCCCTG GGCCGCTCGC GAGGACGTCC 1140 GGCCGCGCCC 1150
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