| Tag | Content |
|---|
EnhancerAtlas ID | HS105-59335 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr4:964860-966990 |
Target genes | | Number: 20 | Name | Ensembl ID |
|
SNPs | | Number: 3 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Zfx | MA0146.2 | chr4:966843-966857 | CAGGCCCCGGCCGC | - | 7.04 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_24252 | chr4:963744-967421 | Colon_Crypt_2 | | SE_25204 | chr4:963623-968354 | Colon_Crypt_3 |
|
Enhancer Sequence | CTGTGGGAAT GAGCACTGTG TGAGTTGGCC CCTGTCCTAC CCAATGGCTG TCCTACCCAG 60
GAAGTTAGAG GCCCCAGGGC AATGACTGCC ATACCCACCA TGCTGCACCA GGGGCCCTGT 120
GGTCCTCGAG TTCCCCCACC ACCCTGCCCA CTCATTGGAG AGAGCCTGCA GCCCAGGAGC 180
CCAGGAGCAA GAACCTGGGT GGTCCTGACC ATCCTGGAGG ACAATGAGTG TATCCTCTCA 240
TCCAGAGAGC AGTCCCTCCC CTTCGCACGT AGGCCCAGCA CTCCTCCTGC CTCTGCAGTT 300
GGGCCTCTCA AGGGGCAGCC CTGGGCTCAC CAGGTTCGCC AGGTGGCAGG GGCTTCTCGG 360
CCTTCGGCAG ATTGGCTTTA CCAAGGACAT CTGTGTCTCA CTCCCCCGAA ACTACGCATA 420
CCCCTAATTG TCCCTGCTAC GTGCTGTGCA CCGTGCCTGA GACCGAGAGC CACCCAAGGC 480
AGGTGAGGGC TCTGGGAGGC AGGAGCCGCT GGGGAGTGGA CAGCCCCAAG CCTCCCAAGG 540
AGCTCTGGCT GTGTGCATAG GACCCAGGGA GCACCTGAGC CGGCGGGGTG CTCAGGAGGG 600
CATAAGAGGA GCAAGCGCCA CACCCCAGCA GTAAAACAGA CAGGAGGGTG GGGCCGGGGC 660
AGAAGGGAGG GCAGGAACCC TGGGCTGGGG CAAAGGCTGC GGGGGCTGGG AGTGGGCAGG 720
GCACCCAGTG ACACAACTGC CAAGACAGCC CCGGGTGAAG GTTGTGCCAC GGAGCCCCAG 780
GCAGTCCAGC TGGGACAGGG AGCTCTTCCA GAAGGCCCCG CTGGTGCCGC CCTTCACCTG 840
CTGCAGCCCT AGCCACCCCA GTCTCCAGAT GGGACCGGGA GAAGCTTCTC CTGGCAGCTT 900
AAGAGAAAAG CTCTGGAAGC AGGCCAGGGT CCACCGAGAG AAGGGGGGAC AGGCAGCACC 960
CAGGTCCCTC CTCTGCCATG GAGACAGGGC CTGCTCACCC CACGCCCCAC GCTTGGGTCT 1020
CCTGGCGGGG AGGGTGCCCT CCTTCCCATA CCGCTGCTGG CCCCTCTTCC ACGGGTGCTG 1080
CCCAGGAGGG CCCTTTTGCC CCCTCCGAAG GGGGAGGGGA CCCGGAGTCT GGCCTCAAGT 1140
CGGGAGCTGC CTCAGCCACA CATGCACACT CCCCACCTCT GGGGAAGCCC CTGGCATCCC 1200
CAGGCAGCAG GCATGGCTGT GCCATGCTCT GACGTGACAA AGAAGCTGGC GGGCCAGGCC 1260
ACCTTGTGCA GCCCTGGGGG TCAGAACAAC CATGCCGTTT CCACCACAGA CGACATCCCC 1320
GTGTGAGGGG ACAGTCTCCT CTGCGGACCC TGACCTGAGT GGACCCCTAT CCCCAGAGAA 1380
AGGCCTGAGG CTAAGGATAG CCCCTCCCAC CTCAGCGTCC CTGGCCAGGA CACAGTAAGT 1440
GTCAAACGTC CAGAACTCCG GTCCTGTCCC TCGCTCCCTC CAGAGGCTGG GCTGTGGTCC 1500
CCCTGTCCCT CGCTCCCTCC AGAGGCTGGG CTGTGGTCCC CCTGTCCCTC GCTCCCTCCA 1560
GAGGCTGGGC TGTAGTCCCC GGGGCCCGCC TGCTTGCCGC GGGGGAAGAT GAGAGCCAGC 1620
CCTGGGAGCA CCCGGGCCCA GAACAGGGAA GGGCTGTCCT CACCCCAGCA AGAGCTGGGC 1680
AGCTGGGTGG AGCAGGGCTG GGACACGCGC ACCGGGACGG CAGGGCCCGG CCTGGCTCTC 1740
CAGGAGGCTG GGACTCTGGG CCACAGCATG AGAAGGGCTA GGGCCAGGGG CCCAGGCCAG 1800
CCCTGCTTAG CCACACCTGC TGCCCCAGCC ACTGGGAGAG GAAGCCGGCC ATGGGGACCC 1860
CAGCTGAGGT CCCGCTCGCA TCAGGCACAG CCCCTGGGTC GCAGCCATCG CGCGGCACTA 1920
TGGAGATGCT GTCCGCACCT CCCAGGTGAG GAAGCCCGCA GCCTGGAGCG GCCCCACGGC 1980
GCACAGGCCC CGGCCGCCCC ACGAAGGCAC GTCCCGCGAG CAGGGCTGGG ACCCCGCCCT 2040
CCACTCCCCC GAAAGCGCCG GTGCCACCTC CGCTCAGGCT CCCGCCCACG GGGCAGAGGC 2100
AGGGCTGCAG CCGGGTAGGC ATCGGGCCCG 2130
|
