| Tag | Content |
|---|
EnhancerAtlas ID | HS178-09316 |
Organism | Homo sapiens |
Tissue/cell | Skeletal_muscle |
Coordinate | chr16:67888860-67890330 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr16:67889492-67889504 | GAATGTTTGTTT | + | 7.22 | | Nr5a2 | MA0505.1 | chr16:67889896-67889911 | GGTGACCTTGAGCAC | - | 6.05 | | ZNF263 | MA0528.1 | chr16:67889796-67889817 | GGGGGATGGGGGAAATGAGAA | + | 6.07 |
|
| | 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 |
| GH16I067854 | chr16 | 67888854 | 67893302 |
|
Enhancer Sequence | GGCAGGATTT CTTTAAGCTG AGGTTGAGCC GAACCTTGTG CTGGGTGCTG GTTTGTTTTT 60
TTTTTTAATT AATGTTTTGA TAGGGCATTT GAGAATGATG TTTGTGTGTT TGCAGTTCAG 120
TTTGAGTTGG CTACCCCTTT CCTGGCTTTG TGATTCTGTG ATTCTCTCTT CCTTTGATCA 180
TATATGGCAG GAATTCTTGA GTCCCTCCCT CGGGGAGCCA GCAGTGTATG GATTATCCTT 240
GGAGTGACTT AGGTCATGTG ATATTATTCA CCCTCTTTTT CCTCACCCTA TCAGCTGGAG 300
TGTGCCCTCC TGGGCAGAAT GCTTTGCTTG GGTCTGGGTT TGGCTGGGAA CGTGTCTTAG 360
TGGCCAAGGG AGAGGGACAC GAGGCCCAGG GTGGCCTGCC TAGGGGCCAC AGGGCTCCTA 420
CTGCTGGCTG ACCAGTGGCC AAGAACTTCT TTTCATTGTC TGGGGCGTTA CTCATTTGTT 480
GCTGTACCTG CTGTGTGCCA GCTCCTTAAG CCCCCAGGCT GGAGACAGGG CTGCTATGGG 540
GATAGGGAAC CCTTATTAGA GAGGGGTTTC TGGGGTACCT GGGAACTGAG GGCTGTTTGT 600
CCCAGTGTCC TCAGTAAACT GGGGGAATTT TGGAATGTTT GTTTCTTAAA GTCTCGAATG 660
ATTCCATCAG AGCCAGTGGG TCTCCCGAGG GCAGAAACTG GAAAGCTTGC TGCCCCAGGA 720
AAGAGCTCTG TGTGGAGATA CTGGTTCCAC TTGCAGGTGG TTTCAGGACT AGGAGAATGC 780
AAATTCTCAG TTGTCCTAAG GTGTAAAGCT GCTTTGACCT GCTGAGTAGG TGCTCAGGTT 840
CTTCCATTCT GAGGCTCCAT GGAGCTTGCT GATTTCATAG GGGAAGACAA GGCCTGGGCT 900
GCATTCCTTG CCACCCGATT TTTTTTTGGC GGGGGGGGGG GATGGGGGAA ATGAGAATAA 960
CTTTATTTCA TTGCGGGGAG TGGGCAGATG TCCAGCCTCA GAACTTCTGG AACTGCTTCT 1020
TGGTGCCAGC GGCCTTGGTG ACCTTGAGCA CGTTGAAGCG TACTGTCTTG CTCAGGGGCC 1080
GGCACTCACC CACTGTTACG ATGTGGCCAA TCTGGACGTC CCTGAAGAAG GTGGACAGGT 1140
GTATGGACAT GTTCTTGTAA CACCTGATTT TGTCACTTAG GTGCTTTCTG CTACTCCACA 1200
TTGGCTCTCA GCTGTTTGCA TCTCGGCCAG TTTTTTTTTG TTGTTGTTGT TTTTTGAGAC 1260
AGTCTCGCTC TGTCGCCTAG GCTGGAGTGC CGTGGTGTGA TCTCAGCTCA CTGCAACCTC 1320
CACCTCCCAG GTTCAAGCAA TTCTCTGCCT CAGCCTCCTG AGTAGCTGGG ATTACAGGCA 1380
CCCACCACCA CGCCTGGCAA ATTTTTATAT TTTTAATAGA GACAGGGTTT CACCATCTTG 1440
GCCAGGCTGG TCTTGAATTC CTGACTTCAT 1470
|
