| Tag | Content |
|---|
EnhancerAtlas ID | HS098-41485 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr4:965150-966990 |
Target genes | | Number: 14 | 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 | CTCTGCAGTT GGGCCTCTCA AGGGGCAGCC CTGGGCTCAC CAGGTTCGCC AGGTGGCAGG 60
GGCTTCTCGG CCTTCGGCAG ATTGGCTTTA CCAAGGACAT CTGTGTCTCA CTCCCCCGAA 120
ACTACGCATA CCCCTAATTG TCCCTGCTAC GTGCTGTGCA CCGTGCCTGA GACCGAGAGC 180
CACCCAAGGC AGGTGAGGGC TCTGGGAGGC AGGAGCCGCT GGGGAGTGGA CAGCCCCAAG 240
CCTCCCAAGG AGCTCTGGCT GTGTGCATAG GACCCAGGGA GCACCTGAGC CGGCGGGGTG 300
CTCAGGAGGG CATAAGAGGA GCAAGCGCCA CACCCCAGCA GTAAAACAGA CAGGAGGGTG 360
GGGCCGGGGC AGAAGGGAGG GCAGGAACCC TGGGCTGGGG CAAAGGCTGC GGGGGCTGGG 420
AGTGGGCAGG GCACCCAGTG ACACAACTGC CAAGACAGCC CCGGGTGAAG GTTGTGCCAC 480
GGAGCCCCAG GCAGTCCAGC TGGGACAGGG AGCTCTTCCA GAAGGCCCCG CTGGTGCCGC 540
CCTTCACCTG CTGCAGCCCT AGCCACCCCA GTCTCCAGAT GGGACCGGGA GAAGCTTCTC 600
CTGGCAGCTT AAGAGAAAAG CTCTGGAAGC AGGCCAGGGT CCACCGAGAG AAGGGGGGAC 660
AGGCAGCACC CAGGTCCCTC CTCTGCCATG GAGACAGGGC CTGCTCACCC CACGCCCCAC 720
GCTTGGGTCT CCTGGCGGGG AGGGTGCCCT CCTTCCCATA CCGCTGCTGG CCCCTCTTCC 780
ACGGGTGCTG CCCAGGAGGG CCCTTTTGCC CCCTCCGAAG GGGGAGGGGA CCCGGAGTCT 840
GGCCTCAAGT CGGGAGCTGC CTCAGCCACA CATGCACACT CCCCACCTCT GGGGAAGCCC 900
CTGGCATCCC CAGGCAGCAG GCATGGCTGT GCCATGCTCT GACGTGACAA AGAAGCTGGC 960
GGGCCAGGCC ACCTTGTGCA GCCCTGGGGG TCAGAACAAC CATGCCGTTT CCACCACAGA 1020
CGACATCCCC GTGTGAGGGG ACAGTCTCCT CTGCGGACCC TGACCTGAGT GGACCCCTAT 1080
CCCCAGAGAA AGGCCTGAGG CTAAGGATAG CCCCTCCCAC CTCAGCGTCC CTGGCCAGGA 1140
CACAGTAAGT GTCAAACGTC CAGAACTCCG GTCCTGTCCC TCGCTCCCTC CAGAGGCTGG 1200
GCTGTGGTCC CCCTGTCCCT CGCTCCCTCC AGAGGCTGGG CTGTGGTCCC CCTGTCCCTC 1260
GCTCCCTCCA GAGGCTGGGC TGTAGTCCCC GGGGCCCGCC TGCTTGCCGC GGGGGAAGAT 1320
GAGAGCCAGC CCTGGGAGCA CCCGGGCCCA GAACAGGGAA GGGCTGTCCT CACCCCAGCA 1380
AGAGCTGGGC AGCTGGGTGG AGCAGGGCTG GGACACGCGC ACCGGGACGG CAGGGCCCGG 1440
CCTGGCTCTC CAGGAGGCTG GGACTCTGGG CCACAGCATG AGAAGGGCTA GGGCCAGGGG 1500
CCCAGGCCAG CCCTGCTTAG CCACACCTGC TGCCCCAGCC ACTGGGAGAG GAAGCCGGCC 1560
ATGGGGACCC CAGCTGAGGT CCCGCTCGCA TCAGGCACAG CCCCTGGGTC GCAGCCATCG 1620
CGCGGCACTA TGGAGATGCT GTCCGCACCT CCCAGGTGAG GAAGCCCGCA GCCTGGAGCG 1680
GCCCCACGGC GCACAGGCCC CGGCCGCCCC ACGAAGGCAC GTCCCGCGAG CAGGGCTGGG 1740
ACCCCGCCCT CCACTCCCCC GAAAGCGCCG GTGCCACCTC CGCTCAGGCT CCCGCCCACG 1800
GGGCAGAGGC AGGGCTGCAG CCGGGTAGGC ATCGGGCCCG 1840
|
