| Tag | Content |
|---|
EnhancerAtlas ID | HS085-00416 |
Organism | Homo sapiens |
Tissue/cell | Heart |
Coordinate | chr11:291110-291940 |
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 | CAGGTGAGCA CTGTACACCC AGCACCAGCC ACACAGCAGG CGACACATGG AGGTCCACGG 60
TCTCTGCCCT CCCTGGGACC AGGGCTATGG TTGGGGAAGC ACAGGGACTG TGGCAAAAGG 120
GAAGAGGCCT GGAAGGTGTG CAGGAGTTTG GTAGAGGAGT GATCTAGGTG AGGGGAATGG 180
AAGGTGCAGA GACCAGAGCT GAGAGGGCCT GAGGCACTTT CCAGAGCGTG GGGAGGGGCC 240
TCCACCAAGG CGAGAAGGGC TGCAGGTCCA GATCACCAGC GTTTGTAGAC AGTAGTGTGG 300
CGCTTGGAGT TTACCTGAGG GCCAGTGGAG CTCCAGGGAC CTATCAGGAC GGGGACCTGT 360
GGGGACTGGG AAGGCCTGTG GGGCTGCGTG GAGCCCGGTA CTGGAGGCCG ACGGGGGTGA 420
CGGGGACGCT GAGGGCACAG AGCGGAGGGG CATGATGGCT GCTGGGCGTG GAGGTGTCGA 480
GAGTGACTGT GCTGGGGCTG CTCCATCGTT GTCTGAGCCT CCCGGTGCTG CCGCTGTGGC 540
CGTTTCTTTG ATGAGGCTCT CAGAGGCCGA GTCATTCACT GCCAGCCTGA AGCTGCCCAT 600
GCGCATATTC GGGCTGGAGC CTCTGAGGCC ACACAAACGC CGGCTGGGGA GGCGAAGTGT 660
GGGGCTGAGC ACCAGAACTC CAGGAGCGTC TGGGCTGGAG ACAGAACTGG GTGGGCAGGT 720
GGGGAGGGCC TGCAGATCTG AGTGGGCAGC CGAGGAGGAA CCCAGAAGAC GCCAGCGATG 780
GAGCTCTGCC GGGGCGGAAT GTGGCCAGGA GGGGCGGGAG CAGTGACGGC 830
|
