| Tag | Content |
|---|
EnhancerAtlas ID | HS062-06009 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr16:411810-412800 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myog | MA0500.1 | chr16:412641-412652 | AACAGCTGCAG | + | 6.02 | | PLAG1 | MA0163.1 | chr16:412178-412192 | CCCCCTGAGGCCCC | - | 6.02 | | Tcf12 | MA0521.1 | chr16:412641-412652 | AACAGCTGCAG | + | 6.62 |
|
| | 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 |
| GH16I000358 | chr16 | 408968 | 415126 |
|
Enhancer Sequence | TCATTCATGT CCAGTGTGTG GGGTCCTTGC CCCTCTCCTG GCCTGTCCGG GGCCACTCTG 60
TGCCCTGCCT TACCCCCAGC AGAGGCAGAA GCACTGGCCT TGCAGCCCCT GCTGAGAGGA 120
GGACTTCAGG TCAGGCTTGC CTCAGGGGCT GAAGGCCAGG CCCAGTCTGG TGGGAAAATA 180
AAGGGTGGGA GCAGTGGAAG CGGGAGCAGG GAGAACTTCC CAGCCCCACT GGGCAGAGCC 240
AAGCTCTCGC CCACCTCAGA CGGCAAAGGC TGCCAGCTTT CTCTCCGCCC ACAGTCCACT 300
CCGCCACCCT CTCGTTAGCT GCGGCCTGTG GAATACGTGC ACGTGCTCAC ACAGTCCCGT 360
CTCACAAGCC CCCTGAGGCC CCTCCCGAGG CCTTGCTCCC TGGACCTTGG GTTCCCACTG 420
GGCAGGACTC TGGGTCTTTG GCCACACTGA GGAGACCGTC TCGCCATCAG TCACACACCT 480
GCGGCTGCAC CCGCTCTCCC CTGGGCTGCA GTGCCCTCTT GCGTCCCAAG AACGCCTCTT 540
CCCTCCAGGG CGCACCAGCA TTGGCCCCTG GCAAAGCTTT CCCGTATGTC TGGAGACGAG 600
GCTTCTCAAC CGTCACCCGT GGACATCCTG GGCACTGCAG GGCACTGAGC ATCCCCGGAA 660
CCACCCCCTG CCCCCAGCCC CGTGACAGCC AGAAACAGTG TTGGCTTGTC CACGCGCTCT 720
GACAGCAGCA CTGCCTGGCC AAGACCCCTT CGAAGGCTTC CCCTAAGCCC GGGAAGCTGA 780
GTCCCACTTC CTGGCCCAGG CCCAGCACCC GATGAGCAGA ATCTGGTGAT GAACAGCTGC 840
AGGACTGCAA GGAGCAAGCG AGAGCCTTGG GCTGCTGCAG CCCAGGGAGG CCACTACCAA 900
GGCCATCAGA GGGACCCGGG ATCCAGGGGA GCCTGGAGCA TGGTCCATGG GGATCCACCT 960
TCAAGAGAGC GACTTCGGGG CCAGTCCCAG 990
|
