| Tag | Content |
|---|
EnhancerAtlas ID | HS012-04026 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr11:62165230-62166550 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr11:62166368-62166379 | AGTGACTCATG | + | 6.14 | | Mecom | MA0029.1 | chr11:62166245-62166259 | TGTTGTCTTATCTC | - | 6.16 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_26858 | chr11:62165319-62171408 | Esophagus | | SE_30860 | chr11:62165065-62171276 | Fetal_Muscle |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I062394 | chr11 | 62161921 | 62170750 |
|
Enhancer Sequence | GGGTGTGTAT ATGCATAATT ATTTTTTCAA AAGTGAGACC ATGCCATGTA TGTTTCAGTT 60
AACACTCTCC ACCATTGCTT GCCAAGAAAT GTTCACCTTA CCTAATATTT GGTCAATATT 120
CAAATTTCCC CAGTTTTCTC AAAAATTGTC TTTTTAGCAG AATTGTTCAA ATCCAGCACC 180
TTTCTTACTG GCACTGCTTG CTGGGTAGTT AGGGCCCCGG GCCCCTCGGC GTCGCATCTT 240
CTGCTTGTCA GGCTGCCCCT CGTTGAGTGA GGGAAGCACC TGGCTGAACA CCACCACAGG 300
CGCTGGGGGC CAGGCCGACC ATTTCAAACA GAAATGTCGA CACCCTGCCA CCGCAGGAGC 360
CATGCAGCGC TGGCCTGTGG GCTGGGGAGG GTTTGGAAAG GGAAATATGG GTTGTGCCAA 420
AGCACAAGGC CCCACCCAGA AGTTTGGCAA AGGGTGACTT GGAGTGAGAA GAGCAGGTGG 480
GGAGCAAGTC CACCCTGCGC CACCACCAGG AAAGGACCTG CCCCCACCCT TCCTCAGCGG 540
CCTCTTCCCA GGTCACTTCC CCTCATACAA AAAGCGTGTG TGCTCCCTTC CCAGCTCCCC 600
TCACCTCAGC CTTTCCCACA CAGCTAGGAG CCAGAGCTAC CCCACGTGCT TGTTGGCCAA 660
AGGGCCACTT TCAGAAGTGT TTACAAATTA CCCCAGGTGG AGGCCACTCA CACCAAATCC 720
AGGAACATTT ACCTCGGGCA TAGAACCACA TTCCCTGGCT ACCCAGTGAA GATCCCCGGG 780
GGCTCGAACC CCCAAATTCT CCCAACTTTC TTTGCAGACA CCAAGTATTT CATCTTTTTT 840
AAAAGTAAGA AACACCAAGG CCAGTTCCCC TCCTCCTCCC ATCTGCTCCC CGCCCCTCCC 900
CTGGGCCCAC TCCCGCTAGC GGCGGCGGCT CATTGCAGGC CGGCATGTCT CCCCGGTGAC 960
CTCACCCCAG ATCTGGCCTT TCTCTGTCAG GCCTCACAAT CTTCCGGGCC ATCTTTGTTG 1020
TCTTATCTCT GGCTTTGGCA CAAATATCAC ACCCTGGATG CCTCATGACT AAAAGTCCAT 1080
CACTTTCCCC AAGCCCTTTC CCTGTCTTCC CTAGAAATTC CAATATATGG CCAGGCGCAG 1140
TGACTCATGC CTGTAATCTC AGTTCTTTGG GAGGCCAAGA CAGGCAGATG ACCTGAGGTT 1200
AGGAGTTGAA GACCAACCTG GCCAACATGG TGAAACCCCG TGTCTACTAA AAATACAGAA 1260
TTAGCTGGAC GTGGTGGTGC AAAACCCCGT GTCTACTAAA ATACAAAATT AACTGGGCGT 1320
|
