| Tag | Content |
|---|
EnhancerAtlas ID | HS029-02768 |
Organism | Homo sapiens |
Tissue/cell | CUTLL1 |
Coordinate | chr11:67231020-67231810 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2C2 | MA0504.1 | chr11:67231356-67231371 | TGCCCTCTGCCCCCA | - | 6.14 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_27544 | chr11:67231042-67233407 | Esophagus | | SE_42089 | chr11:67231301-67232191 | LNCaP |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | TTCTTTTCTT TTTTTTTTTT TAAATAGAGA TGGGTTCTCG CCATGTTGTC CAGGTTGGTC 60
GCGAACTCCT GGGCTCAAGC GATCCTCCCA CCTTGGCCTC TCAAAGTGCT AGGATTACAG 120
GCTTGAGCCA CCGTGCCCGG CCATCCTGGG GTCTTTCAAC AAATTGATAA CTGGTAGCTA 180
CTATGATCTC AGATTTCAGG TTTCTCAAAG ATTCTGTTTC TTGTTTCGTA AGATTCTGAA 240
ATGCTGATGT TCCAAAATTC TGAGATGGTT TGTTTCTAAC GTTCTGCATT TCTAAGTCTT 300
TGACCACTGA GGGTGTCTGT CAGGCGCGGC TTCCTATGCC CTCTGCCCCC AGGTTCTCCC 360
AACCTCTGGG ACTGGGAAGG AGGGCAGTGG GTGGAGGGGG CTGGGCCATT GCCTTGACAT 420
GGCCCACATT CAGGGCTGGC TGTGGCAGCC CAGGGCCCCA GAGCCAGGCT GGAACTAGGA 480
TACCAGCCTC CAGGTCCCAG GCCTGCGTCA TCTCTGCGTG CCCTCGGCCA GGGCCACCAG 540
ACAGAGACGG GCTGGTTGAG TCATCCAAGG GCTGGGGGTG GGGCAGGCTG TTCCGGCCGG 600
CTCCTGGCTG GCAAGGCAGG AGTCCTACGC CCAGCTCTGC CCCTAACATG CCCCGTGCCC 660
TTGGGCAAGC CTCAGCATCA GGGCTGCCAC GCGTTCGGTG GTGCTCGAAG CCCTTCAGCG 720
TCAGGGTCAG TCCTTGGGAG GGGGGCTGTG GTCAGGCTGG TGGGCTGGGC TAGCAGTGGC 780
AGGACAGGAG 790
|
