| Tag | Content |
|---|
EnhancerAtlas ID | HS139-35871 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr22:44525260-44526270 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL2 | MA0478.1 | chr22:44525548-44525559 | GGATGACTCAG | + | 6.32 | | JUNB | MA0490.1 | chr22:44525548-44525559 | GGATGACTCAG | + | 6.14 | | REST | MA0138.2 | chr22:44525741-44525762 | TCCAGCACCTAGGACAGTGCC | + | 8.76 | | SOX10 | MA0442.2 | chr22:44525646-44525657 | TGCTTTGTTTT | - | 6.02 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_65916 | chr22:44524774-44525565 | Pancreatic_islets | | SE_65916 | chr22:44525736-44526687 | Pancreatic_islets |
|
| | 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 |
| GH22I044129 | chr22 | 44525281 | 44525881 |
|
Enhancer Sequence | GACAAACGAA TCCAGTGTCC TCCGCTCCTC TGCCGACTCC TCTTCCTCCA CCCTGGGTGA 60
CGTGGCCATG TTCAGTCTGC GGGGCCGGAT GGTGGCAGGT GCAACGGGGG CGCGTCAGGC 120
TTCCCATCTC CCTGGTGGGC GAGGCTCTCA GACCACCCAG TTCTGTATGA TCCTATCTCT 180
CTCCTTCCTT CTCCAAGCTG CCCTGCTCTG CCCTTTCCAT GGTTGTTGAA CACCTGTGGG 240
ACCTACTTGC TCTCTACTTC CAGGGCGCAA ATTCAGACAG ACAGCTGTGG ATGACTCAGC 300
GAGGAGCTGT TAGATCCAGA TGGAGGGAAA TCAGATGAAT AAGCGGGAAT CGTTTCCACT 360
CCCCTGCAGG ATGTGTTTTG TTGGGCTGCT TTGTTTTTTC TCTTGCAGTC ATTGCCACCC 420
AATCAGATGT TTTTTACGGG TGTTTATCTC CCCACTAGGG ACCTCTGTTA TCTGTGCCAT 480
ATCCAGCACC TAGGACAGTG CCTGTCCCAT AGTAGGTGTT CAGTCCCTAT CTGTGAGCCA 540
ACAAACGCAT GATCGAAGGG GTATTCCGAG CCCAGCAGGC CTTGCTCTAG AATTTTATTA 600
TCTTGAAAGG GATGCCAAAG CTGTTTGTTT TCTAATTGAG GGAGGGGAGG CTGCTGGGGA 660
GATAACACTG AAGACATGGG GGCCTCCAGC TAAAATGTTT TAAACAGAAC TTTGTGCTGG 720
GAACCACTTG CAAAACAGAA ACCCCATTTG TGACTGGCCT GGACTTGATT GCTTTCATGA 780
TGGCATGTCA ATGCCGCGTC ACTGACAGCA GCTGTGTATT GAAGGCTCTG TGCTGAGTGC 840
TTGCAGTCAC CCTCCCAGTG AACCATCTCA CGATGCTCTG TGACGTCGCT TTTGTTGTTT 900
TGCAGAGTGG ATCTATCAGT AAACACTGGA GTCTTAGAAT CGAAGACTAG CAGGGAAACT 960
GGGGGTCCTT CCTGCTGTGT GGCCCTGCAG CGGGCGTGGG GTGGGGCGCT 1010
|
