| Tag | Content |
|---|
EnhancerAtlas ID | HS037-05767 |
Organism | Homo sapiens |
Tissue/cell | ESC |
Coordinate | chr11:291250-291970 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZEB1 | MA0103.3 | chr11:291822-291833 | GGGCAGGTGGG | - | 6.14 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH11I000290 | chr11 | 290656 | 291404 | | GH11I000291 | chr11 | 291621 | 291770 |
|
Enhancer Sequence | CAGGAGTTTG GTAGAGGAGT GATCTAGGTG AGGGGAATGG AAGGTGCAGA GACCAGAGCT 60
GAGAGGGCCT GAGGCACTTT CCAGAGCGTG GGGAGGGGCC TCCACCAAGG CGAGAAGGGC 120
TGCAGGTCCA GATCACCAGC GTTTGTAGAC AGTAGTGTGG CGCTTGGAGT TTACCTGAGG 180
GCCAGTGGAG CTCCAGGGAC CTATCAGGAC GGGGACCTGT GGGGACTGGG AAGGCCTGTG 240
GGGCTGCGTG GAGCCCGGTA CTGGAGGCCG ACGGGGGTGA CGGGGACGCT GAGGGCACAG 300
AGCGGAGGGG CATGATGGCT GCTGGGCGTG GAGGTGTCGA GAGTGACTGT GCTGGGGCTG 360
CTCCATCGTT GTCTGAGCCT CCCGGTGCTG CCGCTGTGGC CGTTTCTTTG ATGAGGCTCT 420
CAGAGGCCGA GTCATTCACT GCCAGCCTGA AGCTGCCCAT GCGCATATTC GGGCTGGAGC 480
CTCTGAGGCC ACACAAACGC CGGCTGGGGA GGCGAAGTGT GGGGCTGAGC ACCAGAACTC 540
CAGGAGCGTC TGGGCTGGAG ACAGAACTGG GTGGGCAGGT GGGGAGGGCC TGCAGATCTG 600
AGTGGGCAGC CGAGGAGGAA CCCAGAAGAC GCCAGCGATG GAGCTCTGCC GGGGCGGAAT 660
GTGGCCAGGA GGGGCGGGAG CAGTGACGGC CTGTCCGGCG CTAGAACGAG GGACCGTGCT 720
|
